| Year |
Citation |
Score |
| 2014 |
Pearson AJ, Zhang S. Stereocontrolled intramolecular iron-mediated tandem [6+2]-ene-type diene/dienol ether double cyclization reactions Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2014.11.129 |
0.486 |
|
| 2013 |
Pearson AJ, Panda S, Bunge SD. Synthesis of a potential intermediate for TMC-95A via an organocatalyzed aldol reaction. The Journal of Organic Chemistry. 78: 9921-8. PMID 24024913 DOI: 10.1021/Jo4017315 |
0.759 |
|
| 2012 |
Pearson AJ, Zhang S, Sun H. Stereocontrolled intramolecular iron-mediated diene/vinyl ether cyclocoupling reactions. The Journal of Organic Chemistry. 77: 8835-9. PMID 22950891 DOI: 10.1021/Jo301721D |
0.469 |
|
| 2011 |
Pearson AJ, Panda S. N-Prolinylanthranilamide pseudopeptides as bifunctional organocatalysts for asymmetric aldol reactions. Organic Letters. 13: 5548-51. PMID 21958056 DOI: 10.1021/Ol202284N |
0.768 |
|
| 2011 |
Pearson AJ, Panda S. N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions Tetrahedron. 67: 3969-3975. DOI: 10.1016/J.Tet.2011.04.033 |
0.75 |
|
| 2010 |
Pearson AJ, Kim EH, Sun H. A synthetic pathway to diquinane and angular triquinane systems via an iron carbonyl promoted tandem [6+2] ene type reaction Tetrahedron. 66: 4943-4946. DOI: 10.1016/J.Tet.2010.05.018 |
0.429 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2010 |
PEARSON AJ, SRINIVASAN K. ChemInform Abstract: Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes. Synthesis of Polyhydroxylated Cycloheptane Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199134079 |
0.351 |
|
| 2009 |
Pearson AJ, Zhou Y. Diels-Alder reactions of cyclopentadienones with aryl alkynes to form biaryl compounds. The Journal of Organic Chemistry. 74: 4242-5. PMID 19422257 DOI: 10.1021/Jo900559N |
0.442 |
|
| 2008 |
Pearson AJ, Ciurea DV, Velankar A. Studies toward the total synthesis of ristocetin A aglycone using arene-ruthenium complexes as S(N)Ar substrates: Construction of an advanced tricyclic intermediate. Tetrahedron Letters. 49: 1922-1926. PMID 18496593 DOI: 10.1016/J.Tetlet.2008.01.094 |
0.799 |
|
| 2008 |
Paramahamsan H, Pearson AJ, Pinkerton NM, Pinkerton AA. 1,5-Asymmetric induction during nucleophilic additions to arenetricarbonylchromium complexes: tricarbonyl(eta(6)-1-methyl-4-{spiro[(1R,2S)-1,7,7-trimethylbicyclo[2.2.1]heptane-3,2'-1,3-dioxolan]-2-yloxy}benzene)chromium. Acta Crystallographica. Section C, Crystal Structure Communications. 64: m147-8. PMID 18391373 DOI: 10.1107/S0108270108004666 |
0.79 |
|
| 2008 |
Pearson AJ, Ciurea DV. Synthesis of a key precursor for orienticin C and model study on ruthenium-mediated macrocyclization. The Journal of Organic Chemistry. 73: 760-3. PMID 18154355 DOI: 10.1021/Jo702245Z |
0.468 |
|
| 2008 |
Paramahamsan H, Pearson AJ, Pinkerton AA, Zhurova EA. Toward an understanding of 1,5-asymmetric induction during nucleophilic addition to (arene)chromium tricarbonyl complexes: Conformational preference of the chromium tricarbonyl tripod for transmission of chirality Organometallics. 27: 900-907. DOI: 10.1021/Om701117R |
0.771 |
|
| 2007 |
Pearson AJ, Sun H. An iron-promoted aldehyde-diene cyclocoupling reaction. The Journal of Organic Chemistry. 72: 7693-700. PMID 17824648 DOI: 10.1021/Jo071124Y |
0.484 |
|
| 2007 |
Pearson AJ, Sun H, Wang X. Dynamic diastereoselectivity during iron carbonyl mediated spirocyclization reactions. The Journal of Organic Chemistry. 72: 2547-57. PMID 17328576 DOI: 10.1021/Jo0625608 |
0.514 |
|
| 2007 |
Pearson AJ, Protasiewicz JD, Updegraff J, Zhang M. Stereoselective conjugate additions of Grignard reagents to cyclopentadienones Tetrahedron Letters. 48: 5569-5572. DOI: 10.1016/J.Tetlet.2007.05.125 |
0.379 |
|
| 2005 |
Pearson AJ, Kwak Y. A new method for the selective oxidation of allylic and benzylic alcohols Tetrahedron Letters. 46: 5417-5419. DOI: 10.1016/J.Tetlet.2005.05.147 |
0.465 |
|
| 2005 |
Pearson AJ, Wang X. A stereospecific intramolecular [4π+4π] cycloaddition reaction between tricarbonyliron-complexed cyclohexadiene and pendant dienes Tetrahedron Letters. 46: 4809-4811. DOI: 10.1016/J.Tetlet.2005.05.045 |
0.618 |
|
| 2005 |
Pearson AJ, Kwak Y. A new method for stereoselective oxidation of chiral 2-pyrrolidino-1- ethanol derivatives to oxazolopyrrolidines using trimethylamine-N-oxide in the presence of iron carbonyls Tetrahedron Letters. 46: 3407-3410. DOI: 10.1016/J.Tetlet.2005.03.101 |
0.53 |
|
| 2005 |
Pearson AJ, Wang X. Dynamic kinetic resolution during iron carbonyl promoted [6+2] ene-type reactions Tetrahedron Letters. 46: 3123-3126. DOI: 10.1016/J.Tetlet.2005.02.166 |
0.565 |
|
| 2005 |
Pearson AJ, Cui S. Ruthenium mediated SNAr reactions in synthetic approaches to ristocetin a aglycon: Preparation of an ABCD ring intermediate Tetrahedron Letters. 46: 2639-2642. DOI: 10.1016/J.Tetlet.2005.02.108 |
0.598 |
|
| 2004 |
Pearson AJ, Ghidu VP. Iron tricarbonyl stabilized pentadienyl cation as initiator for cascade polycyclizations: a diastereoselective entry into octahydrophenanthrenes. The Journal of Organic Chemistry. 69: 8975-8. PMID 15575788 DOI: 10.1021/Jo048557A |
0.806 |
|
| 2004 |
Pearson AJ, Wang X, Dorange IB. Intramolecular iron-mediated diene/olefin cyclocoupling: formation of carbon spirocycles. Organic Letters. 6: 2535-8. PMID 15255684 DOI: 10.1021/Ol040036M |
0.821 |
|
| 2004 |
Pearson AJ, Paramahamsan H, Dudones JD. Vicinal stereocontrol during nucleophilic addition to arene chromium tricarbonyl complexes: formal synthesis of (+/-)-erythro Juvabione. Organic Letters. 6: 2121-4. PMID 15200300 DOI: 10.1021/Ol0494414 |
0.817 |
|
| 2004 |
Mesaros EF, Pearson AJ, Schoffers E. Tricarbonyltris(pyridine)molybdenum(0) and its use as a Mo(0) source for allylmolybdenum(II) complexes Inorganic Syntheses. 34: 104-107. |
0.683 |
|
| 2003 |
Pearson AJ, Wang X. A convenient one-pot procedure to afford bicyclic molecules by stereospecific iron carbonyl mediated [6 + 2] ene-type cyclization: a possible approach to gelsemine. Journal of the American Chemical Society. 125: 13326-7. PMID 14583006 DOI: 10.1021/Ja030407E |
0.584 |
|
| 2003 |
Pearson AJ, Kim JB. Conjugate additions of carbon nucleophiles to cyclopentadienones. Organic Letters. 5: 2457-9. PMID 12841754 DOI: 10.1021/Ol0300571 |
0.417 |
|
| 2003 |
Pearson AJ, Xiao W. Fluorescence and NMR binding studies of N-aryl-N'-(9-methylanthryl)diaza-18-crown-6 derivatives. The Journal of Organic Chemistry. 68: 5369-76. PMID 12816501 DOI: 10.1021/Jo030060Y |
0.422 |
|
| 2003 |
Pearson AJ, Xiao W. Fluorescent photoinduced electron transfer (PET) sensing molecules with p-phenylenediamine as electron donor. The Journal of Organic Chemistry. 68: 5361-8. PMID 12816500 DOI: 10.1021/Jo030059Z |
0.416 |
|
| 2003 |
Pearson AJ, Xiao W. Preparation of N-aryl azacrown ether derivatives, using arene-iron chemistry. The Journal of Organic Chemistry. 68: 2161-6. PMID 12636375 DOI: 10.1021/Jo020527P |
0.57 |
|
| 2003 |
Pearson AJ, Wang X. Double cyclization via intramolecular coupling between cyclohexadiene-Fe(CO)3 complexes and pendant conjugated dienes. Journal of the American Chemical Society. 125: 638-9. PMID 12526656 DOI: 10.1021/Ja0210188 |
0.588 |
|
| 2003 |
Pearson AJ, Kim JB. Cyclopentadienones as intermediates for the synthesis of highly functionalized biaryls Tetrahedron Letters. 44: 8525-8527. DOI: 10.1016/J.Tetlet.2003.08.123 |
0.449 |
|
| 2002 |
Pearson AJ, Ghidu VP. A new paradigm for cationic cyclization of iron tricarbonyl diene complexes with pendant alkenes and arenes. Organic Letters. 4: 4069-71. PMID 12423088 DOI: 10.1021/Ol020177T |
0.809 |
|
| 2002 |
Pearson AJ, Kim JB. Silicon-tethered cyclocarbonylation of alkynes. Organic Letters. 4: 2837-40. PMID 12182568 DOI: 10.1021/Ol020099+ |
0.409 |
|
| 2002 |
Pearson AJ, Mesaros EF. Diastereoselective conjugate additions to pi-allylmolybdenum complexes: a stereocontrolled route to 3,4,5-trisubstituted gamma-butyrolactones. Organic Letters. 4: 2001-4. PMID 12049502 DOI: 10.1021/Ol020043F |
0.761 |
|
| 2002 |
Pearson AJ, Velankar AD, Heo JN. Synthesis of the F-O-G fragment of ristocetin A via ruthenium-promotedintermolecular SNAr reaction Arkivoc. 2002: 49-58. DOI: 10.3998/Ark.5550190.0003.606 |
0.768 |
|
| 2002 |
Pearson AJ, Mesaros EF. Diastereoselective Conjugate Additions to π-Allylmolybdenum Complexes: A Stereocontrolled Route to 3,4,5-Trisubstituted γ-Butyrolactones Organic Letters. 4: 2001-2004. DOI: 10.1021/ol020043f |
0.75 |
|
| 2002 |
Pearson AJ, Wang X. Intramolecular coupling between cyclohexadiene-Fe(CO)3 complexes and pendant alkenes: Formation of azaspiro[5,5]undecane derivatives Tetrahedron Letters. 43: 7513-7515. DOI: 10.1016/S0040-4039(02)01827-0 |
0.594 |
|
| 2001 |
Pearson AJ, Mesaros EF. Stereocontrolled construction of tetrahydrofurans and gamma-butyrolactones using organomolybdenum chemistry. Organic Letters. 3: 2665-8. PMID 11506604 DOI: 10.1021/Ol010121J |
0.768 |
|
| 2001 |
Pearson AJ, Dorange IB. Use of a methoxy substituent in controlling the stereochemistry of intramolecular iron-mediated diene/olefin cyclocoupling. The Journal of Organic Chemistry. 66: 3140-5. PMID 11325280 DOI: 10.1021/Jo010035X |
0.803 |
|
| 2001 |
Pearson AJ, Mesaros EF. Stereocontrolled construction of tetrahydrofurans and γ-butyrolactones using organomolybdenum chemistry Organic Letters. 3: 2665-2668. DOI: 10.1021/ol010121j |
0.672 |
|
| 2001 |
Pearson AJ, Zigmantas S. Synthetic studies on the BCDF ring system of ristocetin A via ruthenium-promoted SNAr reaction Tetrahedron Letters. 42: 8765-8768. DOI: 10.1016/S0040-4039(01)01928-1 |
0.804 |
|
| 2001 |
Pearson AJ, Hwang JJ. Crown-annelated p-phenylenediamine derivatives as electrochemical and fluorescence-responsive chemosensors: Cyclic voltammetry studies Tetrahedron Letters. 42: 3541-3543. DOI: 10.1016/S0040-4039(01)00503-2 |
0.495 |
|
| 2001 |
Pearson AJ, Hwang JJ, Ignatov ME. Crown-annelated p-phenylenediamine derivatives as electrochemical and fluorescence responsive chemosensors: Fluorescence studies Tetrahedron Letters. 42: 3537-3540. DOI: 10.1016/S0040-4039(01)00500-7 |
0.485 |
|
| 2001 |
Pearson AJ, Hwang JJ. Crown-annelated p-phenylenediamine derivatives as electrochemical and fluorescence responsive chemosensors: Synthesis via arene-ruthenium chemistry Tetrahedron Letters. 42: 3533-3536. DOI: 10.1016/S0040-4039(01)00499-3 |
0.604 |
|
| 2001 |
Pearson AJ, Hwang JJ. The triphenylmethyl group as thiol protection during ruthenium-promoted synthesis of tetraalkyl-p-phenylenediamine systems having alkanethiol side chains Tetrahedron. 57: 1489-1495. DOI: 10.1016/S0040-4020(00)01145-5 |
0.548 |
|
| 2001 |
Pearson AJ, Alimardanov AR, Kerber WD. Cationic cyclizations of (diene)iron tricarbonyl complexes with pendant alkenes and arenes Journal of Organometallic Chemistry. 630: 23-32. DOI: 10.1016/S0022-328X(01)00872-5 |
0.811 |
|
| 2000 |
Pearson AJ, Heo JN. Approaches to the fully functionalized DEF ring system of ristocetin A via highly selective ruthenium-promoted S(N)Ar reaction. Organic Letters. 2: 2987-90. PMID 10986089 |
0.577 |
|
| 2000 |
Pearson AJ, Hwang JJ. Preparation of donor-sigma-acceptor molecules using arene-ruthenium chemistry. The Journal of Organic Chemistry. 65: 3466-72. PMID 10843632 DOI: 10.1021/Jo000018S |
0.62 |
|
| 2000 |
Dudones JD, Pearson AJ. The first examples of ester enolate addition across a chiral (alkoxybenzene)-chromium complex π-bond with a remarkable degree of 1,5-asymmetric induction Tetrahedron Letters. 41: 8037-8040. DOI: 10.1016/S0040-4039(00)01407-6 |
0.516 |
|
| 2000 |
Pearson AJ, Heo JN. Synthetic studies on the DEF ring system of ristocetin A via ruthenium-promoted S(N)Ar reaction: Problems and solutions using arylserine-Ru complexes Tetrahedron Letters. 41: 5991-5996. DOI: 10.1016/S0040-4039(00)00855-8 |
0.641 |
|
| 2000 |
Pearson AJ, Belmont PO. Ruthenium-promoted diaryl ether synthesis in the construction of the F- O-G ring system of a teicoplanin model Tetrahedron Letters. 41: 1671-1675. DOI: 10.1016/S0040-4039(00)00030-7 |
0.365 |
|
| 2000 |
Pearson AJ, Katiyar S. Approaches to the synthesis of heptitol derivatives via stereocontrolled functionalization of cycloheptatrienone using organo-iron chemistry Tetrahedron. 56: 2297-2304. DOI: 10.1016/S0040-4020(99)01112-6 |
0.666 |
|
| 1999 |
Pearson AJ, Neagu IB. Lateral Stereocontrol Using pi-Allylmolybdenum Systems: The Use of Methyl Substitution To Effect Conformational Control Leading to High Levels of Stereoselectivity. The Journal of Organic Chemistry. 64: 2890-2896. PMID 11674362 DOI: 10.1021/Jo9900376 |
0.805 |
|
| 1999 |
Pearson AJ, Neagu IB. Lateral stereocontrol using π-allylmolybdenum systems: The use of methyl substitution to effect conformational control leading to high levels of stereoselectivity Journal of Organic Chemistry. 64: 2890-2896. DOI: 10.1021/jo9900376 |
0.774 |
|
| 1998 |
Pearson AJ, Gontcharov AV. Asymmetric Conversion of Arenechromium Complexes to Functionalized Cyclohexenones: Progress toward Defining an Optimum Chiral Auxiliary. The Journal of Organic Chemistry. 63: 152-162. PMID 11674056 DOI: 10.1021/Jo971676O |
0.498 |
|
| 1998 |
Pearson AJ, Alimardanov A. Studies on intramolecular coupling of tricarbonyl(diene)iron systems with pendant olefinic groups: Configurational requirements for reactions of acyclic diene complexes and mechanistic implications Organometallics. 17: 3739-3746. DOI: 10.1021/Om980323S |
0.793 |
|
| 1998 |
Pearson AJ, Alimardanov A, Alan Pinkerton A, Parrish DA. Intramolecular Coupling Reactions of Allylic Thioesters with Diene Iron Tricarbonyl Systems Journal of Organic Chemistry. 63: 6610-6618. DOI: 10.1021/Jo980773U |
0.785 |
|
| 1998 |
Pearson AJ, Chelliah MV. Synthesis of a model bicyclic CDE ring system of ristocetin A and observation of a facile inversion of configuration in a 16-membered DE ring model Journal of Organic Chemistry. 63: 3087-3098. DOI: 10.1021/Jo980060B |
0.384 |
|
| 1998 |
Pearson AJ, Babu M. Observations on regioselectivity during the addition of carbon nucleophiles to isoprene-Mo(CO)2Tp cationic complex Tetrahedron Letters. 39: 6273-6276. DOI: 10.1016/S0040-4039(98)01332-X |
0.436 |
|
| 1998 |
Pearson AJ, Vickerman RJ. Conversion of an amine-substituted amine-manganese tricarbonyl complex to a functionalized cyclohexenone Tetrahedron Letters. 39: 5931-5932. DOI: 10.1016/S0040-4039(98)01214-3 |
0.469 |
|
| 1998 |
Pearson AJ, Alimardanov A, Pinkerton AA, Fouchard DM, Kirschbaum K. Stereocontrolled cyclization of unactivated alkene onto cationic dienyl iron tricarbonyl systems Tetrahedron Letters. 39: 5919-5922. DOI: 10.1016/S0040-4039(98)01211-8 |
0.77 |
|
| 1998 |
Pearson AJ, Douglas AR. Demetalation of dicarbonyl(π-allyl)[hydridotris(pyrazolyl)borato]molybdenum complexes via lactonization Organometallics. 17: 1446-1448. |
0.698 |
|
| 1997 |
Pearson AJ, Zhang P, Bignan G. Synthesis of an Epimer of a 16-Membered Ring Model for Teicoplanin: Confirmation of Epimerization during Cycloamidation. The Journal of Organic Chemistry. 62: 4536-4538. PMID 11671792 DOI: 10.1021/Jo970508T |
0.353 |
|
| 1997 |
Pearson AJ, Yao X. Synthesis of Hydroazulene Derivatives via Iron Carbonyl-Promoted Cyclocarbonylation of 1,8-Diynes Synlett. 1997: 1281-1282. DOI: 10.1055/S-1997-1026 |
0.389 |
|
| 1997 |
Pearson AJ, Schoffers E. Tricarbonyltris(pyridine)molybdenum: A convenient reagent for the preparation of (π-allyl)molybdenum complexes Organometallics. 16: 5365-5367. DOI: 10.1021/Om970473N |
0.507 |
|
| 1997 |
Pearson AJ, Neagu IB, Pinkerton AA, Kirschbaum K, Hardie MJ. Studies on lateral stereocontrol using the (π-Allyl)molybdenum system Organometallics. 16: 4346-4354. DOI: 10.1021/Om970466Z |
0.829 |
|
| 1997 |
Pearson AJ, Fang X. A synthesis of (±)-stemodinone: An application of organoiron chemistry to the construction of sterically congested quaternary carbon centers Journal of Organic Chemistry. 62: 5284-5292. DOI: 10.1021/Jo9705475 |
0.436 |
|
| 1997 |
Pearson AJ, Gelormini AM. Manipulation of the reduction potentials of Wurster's blue derivatives via steric and conformational effects Tetrahedron Letters. 38: 5123-5126. DOI: 10.1016/S0040-4039(97)01091-5 |
0.39 |
|
| 1997 |
Pearson AJ, Gontcharov AV, Zhu PY. Chiral auxiliary-promoted asymmetric nucleophile additions to arene-manganese tricarbonyl complexes Tetrahedron. 53: 3849-3862. DOI: 10.1016/S0040-4020(97)00006-9 |
0.513 |
|
| 1997 |
Pearson AJ, Sun L. An application of arene-iron chemistry in the synthesis of a novel liquid crystalline polymer Journal of Polymer Science, Part a: Polymer Chemistry. 35: 447-453. DOI: 10.1002/(Sici)1099-0518(199702)35:3<447::Aid-Pola7>3.0.Co;2-P |
0.443 |
|
| 1996 |
Pearson AJ, Zhang P, Lee K. Application of Arene-Ruthenium Chemistry to a Formal Total Synthesis of OF 4949 III. The Journal of Organic Chemistry. 61: 6581-6586. PMID 11667524 DOI: 10.1021/Jo960956L |
0.41 |
|
| 1996 |
Pearson AJ, Bignan G, Zhang P, Chelliah M. Cycloetherification Reactions of Areneruthenium Complexes: Construction of a 16-Membered Cyclic Peptide Model for Teicoplanin. The Journal of Organic Chemistry. 61: 3940-3941. PMID 11667263 DOI: 10.1021/Jo960435Y |
0.378 |
|
| 1996 |
Pearson AJ, Gontcharov AV, Woodgate PD. Studies on asymmetric conversion of arenes to functionalized cyclohexenones via chiral auxiliary-promoted nucleophilic additions to arene-chromium complexes Tetrahedron Letters. 37: 3087-3088. DOI: 10.1016/0040-4039(96)00367-X |
0.488 |
|
| 1996 |
Pearson AJ, Bignan G. Studies on the applications of arene-ruthenium complexes in synthetic approaches to vancomycin: A mild procedure for the selective formation of chlorinated aryl ethers and triaryl diethers Tetrahedron Letters. 37: 735-738. DOI: 10.1016/0040-4039(95)02301-1 |
0.496 |
|
| 1995 |
Pearson AJ, Milletti MC, Zhu PY. Observations on selectivity reversal during chiral auxiliary-directed asymmetric nucleophile additions to arene-manganese tricarbonyl complexes Journal of the Chemical Society, Chemical Communications. 853-854. DOI: 10.1039/C39950000853 |
0.41 |
|
| 1995 |
Pearson AJ, Lee K. Synthesis of a 16-membered cyclic peptide model of the BCF rings of ristocetin a using arene-ruthenium chemistry coupled with cycloamidation The Journal of Organic Chemistry. 60: 7153-7160. DOI: 10.1021/Jo00127A020 |
0.338 |
|
| 1995 |
Pearson AJ, Gelormini AM. Selective arylation of diols using arene-iron chemistry The Journal of Organic Chemistry. 60: 281-284. DOI: 10.1021/Jo00106A053 |
0.358 |
|
| 1994 |
Pearson AJ, Manoj Babu MK. Reactions of alkyllithium and grignard reagents with (cyclopentadienyl)dicarbonyl(2-methylbutadiene)molybdenum: Observations of solvent effects on regioselectivity Organometallics. 13: 2539-2541. DOI: 10.1021/Om00019A001 |
0.408 |
|
| 1994 |
Pearson AJ, Dubbert RA. Cyclocarbonylation of 1,6-enynes promoted by iron carbonyls Organometallics. 13: 1656-1661. DOI: 10.1021/Om00017A024 |
0.314 |
|
| 1994 |
Pearson AJ, Shively RJ. Iron Carbonyl Promoted Cyclocarbonylation of 3-Hydroxy .alpha.,.omega.-Diynes To Give (Cyclopentadienone)Iron Tricarbonyl Complexes Organometallics. 13: 578-584. DOI: 10.1021/Om00014A032 |
0.345 |
|
| 1994 |
Pearson AJ, Chang K, McConville DB, Youngs WJ. Chiral-auxiliary-directed asymmetric tricarbonyliron complexation of dienes Organometallics. 13: 4-5. DOI: 10.1021/Om00013A002 |
0.442 |
|
| 1994 |
Pearson AJ, Gelormini AM. Applications of arene -iron chemistry to polymer synthesis: Preparation and polymerization of novel triaryl diether monomers Macromolecules. 27: 3675-3677. DOI: 10.1021/Ma00091A034 |
0.32 |
|
| 1994 |
Pearson AJ, Gelormini AM. Studies on selective nucleophilic substitution reactions of [(cyclopentadienyl)(1,3- and 1,4-dichlorobenzene)Fe]+PF6 - complexes: Applications to the synthesis of polymer monomers Journal of Organic Chemistry. 59: 4561-4570. DOI: 10.1021/Jo00095A036 |
0.481 |
|
| 1994 |
Pearson AJ, Shin H. Synthesis of a 14-membered cyclic peptide model of the CFG rings of ristocetin A and observations on atropdiastereoisomerism Journal of Organic Chemistry. 59: 2314-2323. DOI: 10.1021/Jo00088A010 |
0.453 |
|
| 1994 |
Pearson AJ, Lee K. A formal total synthesis of the ACE inhibitor K-13. An application of arene-ruthenium chemistry to complex chemical synthesis Journal of Organic Chemistry. 59: 2304-2313. DOI: 10.1021/Jo00088A009 |
0.442 |
|
| 1993 |
Pearson AJ, Chang K. Organoiron-templated stereocontrolled alkylation of enolates: Functionalization of cycloheptadienones to give useful synthetic building blocks Journal of Organic Chemistry. 58: 1228-1237. DOI: 10.1021/Jo00057A041 |
0.447 |
|
| 1993 |
Pearson AJ, Zhu PY, Youngs WJ, Bradshaw JD, McConville DB. Chiral auxiliary-directed asymmetric nucleophile additions to arene-manganese tricarbonyl complexes Journal of the American Chemical Society. 115: 10374-10375. DOI: 10.1021/Ja00075A070 |
0.481 |
|
| 1993 |
Pearson AJ, Balasubramanian S, Srinivasan K. Stereocontrolled functionalization of cyclooctadiene using organoiron chemistry Tetrahedron. 49: 5663-5672. DOI: 10.1016/S0040-4020(01)87275-6 |
0.366 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/S-1992-21555 |
0.434 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereocontrolled Functionalization of Cycloheptatrieneiron Complexes via Consecutive Electrophile/Nucleophile Additions Synlett. 1992: 983-984. DOI: 10.1055/s-1992-21555 |
0.323 |
|
| 1992 |
Pearson AJ, Shively RJ, Dubbert RA. Iron carbonyl promoted conversion of .alpha.,.omega.-diynes to (cyclopentadienone)iron complexes Organometallics. 11: 4096-4104. DOI: 10.1021/Om00060A028 |
0.341 |
|
| 1992 |
Pearson AJ, Gelormini AM, Pinkerton AA. Preparation of optically pure tricarbonylcyclohexadienyliron complexes: use of a trifluoromethyl group as a regiodirector during hydride abstraction Organometallics. 11: 936-938. DOI: 10.1021/Om00038A065 |
0.352 |
|
| 1992 |
Pearson AJ, Burello MP. Preparation and reactions of tricarbonyliron complexes of methyl cycloheptadienecarboxylates and methylcycloheptadienes Organometallics. 11: 448-456. DOI: 10.1021/Om00037A072 |
0.477 |
|
| 1992 |
Pearson AJ, Srinivasan K. Approaches to the synthesis of heptitol derivatives via iron-mediated stereocontrolled functionalization of cycloheptatrienone The Journal of Organic Chemistry. 57: 3965-3973. DOI: 10.1021/Jo00040A043 |
0.494 |
|
| 1992 |
Pearson AJ, Park JG, Zhu PY. Studies on selective nucleophilic substitution reactions of [(cyclopentadienyl)(1,3-dichlorobenzene)M]+ PF6- complexes (M = iron, ruthenium) The Journal of Organic Chemistry. 57: 3583-3589. DOI: 10.1021/Jo00039A015 |
0.42 |
|
| 1992 |
Pearson AJ, Mallik S, Pinkerton AA, Adams JP, Zheng S. Stereocontrolled functionalization of 1,5-cyclooctadiene using organomolybdenum chemistry Journal of Organic Chemistry. 57: 2910-2917. DOI: 10.1021/Jo00036A028 |
0.453 |
|
| 1992 |
Pearson AJ, Park JG. Model studies on the synthesis of carboxylate-binding pocket analogs of vancomycin using arene-ruthenium chemistry Journal of Organic Chemistry. 57: 1744-1752. DOI: 10.1021/Jo00032A028 |
0.5 |
|
| 1992 |
Pearson AJ, Srinivasan K. Stereo- and regiocontrolled multiple functionalization of cyclooctadiene using organoiron chemistry. Tetrahedron Letters. 33: 7295-7298. DOI: 10.1016/S0040-4039(00)60170-3 |
0.4 |
|
| 1992 |
Pearson AJ, Shin H. Studies on ristocetin A. A synthesis of protected ristomycinic acid using organomanganese chemistry Tetrahedron. 48: 7527-7538. DOI: 10.1016/S0040-4020(01)90366-7 |
0.511 |
|
| 1991 |
Pearson AJ, Chang K. Stereocontrolled multiple functionalization of cycloheptadienoneiron complexes via enolate alkylation Journal of the Chemical Society, Chemical Communications. 394-396. DOI: 10.1039/C39910000394 |
0.449 |
|
| 1991 |
Pearson AJ, Srinivasan K. Stereocontrolled functionalization of cycloheptatrieneiron complexes. Synthesis of polyhydroxylated cycloheptane derivatives Journal of the Chemical Society, Chemical Communications. 392-394. DOI: 10.1039/C39910000392 |
0.352 |
|
| 1991 |
Pearson AJ, Dubbert RA. Intramolecular alkyne–alkyne and alkyne–alkene couplings promoted by iron carbonyls Journal of the Chemical Society, Chemical Communications. 202-203. DOI: 10.1039/C39910000202 |
0.371 |
|
| 1991 |
Pearson AJ, Bruhn PR. Studies on the synthesis of aryl ethers using arene-manganese chemistry Journal of Organic Chemistry. 56: 7092-7097. DOI: 10.1021/Jo00025A026 |
0.551 |
|
| 1990 |
Pearson AJ, Lee S, Gouzoules F. Synthesis of a deoxyristomycinic acid derivative using organomanganese chemistry Journal of the Chemical Society-Perkin Transactions 1. 2251-2254. DOI: 10.1039/P19900002251 |
0.513 |
|
| 1990 |
Pearson AJ, Roden BA. An approach to the cyclohexyl moiety of the immunosuppressive agent FK-506 Journal of the Chemical Society-Perkin Transactions 1. 723-725. DOI: 10.1039/P19900000723 |
0.383 |
|
| 1990 |
Pearson AJ, Mallik S, Mortezaei R, Perry MWD, Shively RJ, Youngs WJ. Stereocontrol during the alkylation of enolates attached to .pi.-allyl-Mo(CO)2Cp systems Journal of the American Chemical Society. 112: 8034-8042. DOI: 10.1021/Ja00178A028 |
0.473 |
|
| 1990 |
Pearson AJ, Holden MS. Preparation and reactions of tricarbonyl(3-trimethylstannylcycloheptadienyl)iron hexafluorophosphate and tricarbonyl(3-trimethylsilylcycloheptadienyl)iron hexafluorophosphate Journal of Organometallic Chemistry. 383: 307-319. DOI: 10.1016/0022-328X(90)85139-P |
0.707 |
|
| 1989 |
Pearson AJ, Park JG, Yang SH, Chuang Y. A mild procedure for the selective formation of aryl ethers and triaryl diethers using arene–M–CP cations (M = Fe, Ru; Cp =η5-cyclopentadienyl) Journal of the Chemical Society, Chemical Communications. 1363-1364. DOI: 10.1039/C39890001363 |
0.493 |
|
| 1989 |
Pearson AJ, Burello MP. Preparation and reactions of methoxycarbonyl-substituted cycloheptadienyliron tricarbonyl cations: unusual regiochemistry during the addition of stabilized enolate nucleophiles Journal of the Chemical Society, Chemical Communications. 1332-1333. DOI: 10.1039/C39890001332 |
0.483 |
|
| 1989 |
Pearson AJ, Bruhn PR, Gouzoules F, Lee S. Stereoselective synthesis of arylglycine derivatives using arene–manganese tricarbonyl complexes Journal of the Chemical Society, Chemical Communications. 659-661. DOI: 10.1039/C39890000659 |
0.515 |
|
| 1989 |
Pearson AJ, Perry MWD. Synthesis and reactions of η3-5-oxocyclohexenyl(dicarbonyl)(η5-cyclopentadienyl)molybdenum Journal of the Chemical Society, Chemical Communications. 389-391. DOI: 10.1039/C39890000389 |
0.508 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/Jo00282A035 |
0.489 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, Khetani VD, Roden BA. Asymmetric induction during the reactions of dienyl-iron and diene-molybdenum complexes with chiral N-acyloxazolidinone enolates The Journal of Organic Chemistry. 54: 5141-5147. DOI: 10.1021/jo00282a035 |
0.389 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/Jo00280A039 |
0.472 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, O'Brien MK. Trichothecene synthesis using organoiron complexes: diastereoselective total syntheses of (.+-.)-trichodiene, (.+-.)-12,13-epoxytrichothec-9-ene, and (.+-.)-trichodermol The Journal of Organic Chemistry. 54: 4663-4673. DOI: 10.1021/jo00280a039 |
0.368 |
|
| 1989 |
Pearson AJ, Lai YS, Lu W, Pinkerton AA. Stereocontrolled functionalization of cycloheptadiene using organometallic chemistry: synthesis of the (+)-Prelog-Djerassi lactone and a tylosin subunit The Journal of Organic Chemistry. 54: 3882-3893. DOI: 10.1021/Jo00277A027 |
0.362 |
|
| 1989 |
Pearson AJ, Khetani VD. Construction of quaternary carbon centers using organomolybdenum chemistry Journal of the American Chemical Society. 111: 6778-6789. DOI: 10.1021/Ja00199A043 |
0.356 |
|
| 1989 |
Pearson AJ, Zettler MW. Intramolecular coupling between tricarbonyl(diene)iron complexes and pendant alkenes Journal of the American Chemical Society. 111: 3908-3918. DOI: 10.1021/Ja00193A023 |
0.427 |
|
| 1989 |
O'Brien MK, Pearson AJ, Pinkerton AA, Schmidt W, Willman K. A total synthesis of (.+-.)-trichodermol Journal of the American Chemical Society. 111: 1499-1501. DOI: 10.1021/Ja00186A057 |
0.337 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/Ja00183A024 |
0.476 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Blystone SL, Nar H, Pinkerton AA, Roden BA, Yoon J. A study of asymmetric induction during the addition of enolate nucleophiles, having sulfoximine chiral auxiliaries, to diene-molybdenum and dienyliron complexes Journal of the American Chemical Society. 111: 134-144. DOI: 10.1021/ja00183a024 |
0.373 |
|
| 1989 |
Pearson AJ, Mortezaei R. Multiple stereocontrol using organotransition metal templates: Alkylation of enolates Tetrahedron Letters. 30: 5049-5052. DOI: 10.1016/S0040-4039(01)93444-6 |
0.465 |
|
| 1988 |
Pearson AJ, Lai Y. A synthesis of the (+)-Prelog–Djerassi lactone Journal of the Chemical Society, Chemical Communications. 442-443. DOI: 10.1039/C39880000442 |
0.313 |
|
| 1988 |
Pearson AJ, Khetani VD. Construction of quaternary carbon centers using organomolybdenum chemistry. Synthesis of a trichothecene intermediate Journal of Organic Chemistry. 53: 3395-3396. DOI: 10.1021/Jo00249A063 |
0.334 |
|
| 1988 |
Pearson AJ, O'Brien MK. Alkylation of silyl ketene acetals with dienyliron complexes: application in the formation of quaternary carbon centers. Tetrahedron Letters. 29: 869-872. DOI: 10.1016/S0040-4039(00)82469-7 |
0.497 |
|
| 1987 |
Pearson AJ, O'Brien MK. Reaction of tin enolates with substituted tricarbonylcyclohexadienyliumiron hexafluorophosphate electrophiles: diastereoselective synthesis of (±)-trichodiene Journal of the Chemical Society, Chemical Communications. 1445-1447. DOI: 10.1039/C39870001445 |
0.437 |
|
| 1987 |
Pearson AJ, Zettler MW. Control of absolute stereochemistry during ene-type coupling between diene–Fe(CO)3 groups and alkenes Journal of the Chemical Society, Chemical Communications. 1243-1245. DOI: 10.1039/C39870001243 |
0.423 |
|
| 1987 |
Pearson AJ, Zettler M, Pinkerton AA. Intramolecular ene-type reaction between a diene-Fe(CO)3 complex and alkene units Journal of the Chemical Society, Chemical Communications. 264-266. DOI: 10.1039/C39870000264 |
0.384 |
|
| 1987 |
Pearson AJ, Zettler M, Pinkerton AA. Intramolecular ene-type reaction between a diene-Fe(CO)3 complex and alkene units Journal of the Chemical Society, Chemical Communications. 264-266. DOI: 10.1039/C39870000264 |
0.384 |
|
| 1987 |
Pearson AJ, Zettler M, Pinkerton AA. Intramolecular ene-type reaction between a diene-Fe(CO)3 complex and alkene units Journal of the Chemical Society, Chemical Communications. 264-266. DOI: 10.1039/C39870000264 |
0.384 |
|
| 1987 |
Pearson AJ, Zettler M, Pinkerton AA. Intramolecular ene-type reaction between a diene-Fe(CO)3 complex and alkene units Journal of the Chemical Society, Chemical Communications. 264-266. DOI: 10.1039/C39870000264 |
0.384 |
|
| 1987 |
Pearson AJ, Zettler M, Pinkerton AA. Intramolecular ene-type reaction between a diene-Fe(CO)3 complex and alkene units Journal of the Chemical Society, Chemical Communications. 264-266. DOI: 10.1039/C39870000264 |
0.384 |
|
| 1987 |
Pearson AJ, Chen Y, Daroux ML, Tanaka AA, Zettler M. Free radical coupling reactions of organoiron complexes: electrochemical studies and preliminary cross coupling experiments Journal of the Chemical Society, Chemical Communications. 155-157. DOI: 10.1039/C39870000155 |
0.379 |
|
| 1986 |
Pearson AJ, Khetani VD. Molybdenum-stabilized carbanions: a novel decyanation reaction with stereoelectronic requirement suggesting participation of the η3-allyl–Mo(CO)2(cp)(cp =η5-C5H5) moiety in stabilizing neighbouring carbanions Journal of the Chemical Society, Chemical Communications. 1772-1774. DOI: 10.1039/C39860001772 |
0.419 |
|
| 1986 |
Pearson AJ, Yoon J. Chiral recognition during the reaction of dienyliron complexes with sulphoximine-stabilized enolates Journal of the Chemical Society, Chemical Communications. 1467-1469. DOI: 10.1039/C39860001467 |
0.52 |
|
| 1986 |
Pearson AJ, Kole SL, Yoon J. Stereocontrolled double functionalization of (cyclohexadiene)- and (cycloheptadiene)iron complexes via oxidative cyclization techniques Organometallics. 5: 2075-2081. DOI: 10.1021/Om00141A025 |
0.368 |
|
| 1986 |
Pearson AJ, Hsu SY. Ester-directed alkene functionalization. A potential approach to trichothecene synthesis The Journal of Organic Chemistry. 51: 2505-2511. DOI: 10.1021/Jo00363A019 |
0.344 |
|
| 1986 |
Pearson AJ, Bruhn PR, Hsu SY. Preparation of diaryl ethers from tyrosine or 4-hydroxyphenylglycine using organomanganese chemistry Journal of Organic Chemistry. 51: 2137-2139. DOI: 10.1021/Jo00361A043 |
0.41 |
|
| 1986 |
Pearson AJ, Holden MS, Simpson RD. Generation and reactions of carbanions in the presence of a neighboring η3-allyl-Mo(CO)2Cp moiety; A novel rearrangement suggesting participation of Mo in carbanion stabilization. Tetrahedron Letters. 27: 4121-4124. DOI: 10.1016/S0040-4039(00)84926-6 |
0.718 |
|
| 1986 |
Pearson AJ, Bansal HS. Controlled functionalization of cyclohepta-1,3-diene: Conformational analysis of cycloheptenones and derived cycloheptadienolate anions Tetrahedron Letters. 27: 287-290. DOI: 10.1016/S0040-4039(00)83998-2 |
0.355 |
|
| 1986 |
Pearson AJ, Bruhn PR, Hsu S-. Preparation of Diaryl Ethers from Tyrosine or 4-Hydroxyphenylglycine Using Organomanganese Chemistry. Cheminform. 17. DOI: 10.1002/Chin.198651152 |
0.371 |
|
| 1985 |
Pearson AJ, Chen Y, Han GR, Hsu S, Ray T. A new method for the oxidation of alkenes to enones. An efficient synthesis of Δ5-7-oxo steroids Journal of the Chemical Society-Perkin Transactions 1. 16: 267-273. DOI: 10.1039/P19850000267 |
0.375 |
|
| 1985 |
Pearson AJ, Chen B. A convenient preparation of dicarbonyl(.eta.5-cycloheptadienyl)(triphenyl phosphite)iron tetrafluoroborate, a potential macrolide antibiotic precursor The Journal of Organic Chemistry. 50: 2587-2588. DOI: 10.1021/Jo00214A040 |
0.332 |
|
| 1985 |
Pearson AJ, Khan MNI, Clardy JC, Cun-heng H. Stereocontrolled functionalization in the cyclohexane ring using organomolybdenum chemistry Journal of the American Chemical Society. 107: 2748-2757. DOI: 10.1021/Ja00295A030 |
0.38 |
|
| 1985 |
Pearson AJ, Khan MNI. Stereo- and regio-controlled functionalization of cycloheptene using organomolybdenum chemistry Tetrahedron Letters. 26: 1407-1410. DOI: 10.1016/S0040-4039(00)99057-9 |
0.492 |
|
| 1985 |
Pearson AJ, Ray T. A convergent organoiron approach to steroid synthesis Tetrahedron Letters. 26: 2981-2984. DOI: 10.1016/S0040-4039(00)98597-6 |
0.355 |
|
| 1985 |
Pearson AJ, Ray T. A convergent organoiron approach to steroid synthesis Tetrahedron Letters. 26: 2981-2984. DOI: 10.1016/S0040-4039(00)98597-6 |
0.355 |
|
| 1985 |
Pearson AJ, Yoon J. Effects of licand environment on nucleophile addition to cyclohexadienyliron cations. Tetrahedron Letters. 26: 2399-2402. DOI: 10.1016/S0040-4039(00)94837-8 |
0.455 |
|
| 1985 |
Pearson AJ, Ray T. New strategies for the construction of macrolide antibiotic subunits using organoiron precursors Tetrahedron. 41: 5765-5770. DOI: 10.1016/S0040-4020(01)91415-2 |
0.391 |
|
| 1985 |
Pearson AJ, Perrior TR. Organoiron complexes in organic synthesis Journal of Organometallic Chemistry. 285: 253-265. DOI: 10.1016/0022-328X(85)87372-1 |
0.473 |
|
| 1985 |
Pearson AJ, Richards IC, Gardner DV. Organoiron Complexes In Organic Synthesis. 33. Tricarbonylcyclohexadienyliron N Complexes As Aryl Cation Equivalents: A Formal Synthesis Of (.+-.)-O-Methyljoubertiamine Cheminform. 16. DOI: 10.1002/Chin.198514341 |
0.45 |
|
| 1984 |
Pearson AJ. Iron-stabilized carbocations as intermediates for organic synthesis. Science (New York, N.Y.). 223: 895-901. PMID 17781612 DOI: 10.1002/Chin.198428370 |
0.347 |
|
| 1984 |
Eisenstein O, Butler WM, Pearson AJ. A theoretical study of the formation and reactivity of substituted cyclohexadienyliron complexes. The structures and reactivities of tricarbonyl(2-methoxycyclohexadienyl)iron cation and tricarbonyl(1-methyl-4-methoxycyclohexadienyl)iron cation Organometallics. 3: 1150-1157. DOI: 10.1021/Om00086A003 |
0.405 |
|
| 1984 |
Pearson AJ, Richards IC, Gardner DV. Organoiron complexes in organic synthesis. 33. Tricarbonylcyclohexadienyliron complexes as aryl cation equivalents: a formal synthesis of (.+-.)-O-methyljoubertiamine Journal of Organic Chemistry. 49: 3887-3891. DOI: 10.1021/Jo00195A003 |
0.45 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/Ja00318A072 |
0.426 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MNI. Stereocontrolled lactone synthesis using diene-molybdenum chemistry Journal of the American Chemical Society. 106: 1872-1873. DOI: 10.1021/ja00318a072 |
0.314 |
|
| 1984 |
Pearson AJ, Khan MI. Stereocontrolled functionalization of cyclohexene using organomolybdenum chemistry Tetrahedron Letters. 25: 3507-3510. DOI: 10.1016/S0040-4039(01)91061-5 |
0.491 |
|
| 1984 |
Pearson AJ, Chen Y, Hsu S, Ray T. Oxidation of alkenes to enones using tert-butyl hydroperoxide in the presence of chromium carbonyl catalysts Tetrahedron Letters. 25: 1235-1238. DOI: 10.1016/S0040-4039(01)80121-0 |
0.312 |
|
| 1984 |
Pearson AJ, Bruhn P, Richards IC. Regio- and stereocontrolled functionalization of the seven-membered ring using organomanganese chemistry Tetrahedron Letters. 25: 387-390. DOI: 10.1016/S0040-4039(00)99890-3 |
0.459 |
|
| 1984 |
Birch AJ, Raverty WD, Hsu SY, Pearson AJ. Acetylation of dicarbonyl(η4-cyclohexadiene)triphenyl- phosphineiron Journal of Organometallic Chemistry. 260: C59-C62. DOI: 10.1016/S0022-328X(00)99488-9 |
0.667 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/ijch.198400016 |
0.37 |
|
| 1984 |
Pearson AJ, Bruhn PR, Richards IC. Tricarbonyl(η6-Cycloheptatriene)manganese Hexafluorophosphate: Reactions with Enolate Nucleophiles and Decomplexation of the Product Dienyl Complexes Israel Journal of Chemistry. 24: 93-98. DOI: 10.1002/Chin.198450308 |
0.474 |
|
| 1983 |
Pearson AJ. Natural products synthesis using organoiron complexes Pure and Applied Chemistry. 55: 1767-1779. DOI: 10.1351/Pac198355111767 |
0.402 |
|
| 1983 |
Pearson AJ, Perrior TR, Griffin DA. Organoiron complexes in organic synthesis. Part 27. Synthesis and reactivity of tricarbonyliron derivatives of 1,2-disubstituted 4-alkoxycyclohexadienylium cations Journal of the Chemical Society-Perkin Transactions 1. 14: 625-631. DOI: 10.1039/P19830000625 |
0.509 |
|
| 1983 |
Pearson AJ, Rees DC, Thornber CW. Synthetic approaches to C-18 oxygenated aspidosperma alkaloids via Organoiron Complexes Journal of the Chemical Society-Perkin Transactions 1. 619-623. DOI: 10.1039/P19830000619 |
0.385 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/Ja00351A064 |
0.416 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Kole SH, Chen B. Organoiron complexes in organic synthesis. 30. Approach to stereochemically defined cycloheptadiene derivatives using organoiron chemistry Journal of the American Chemical Society. 105: 4483-4484. DOI: 10.1021/ja00351a064 |
0.301 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.463 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Direct carbomethoxymethylation of organoiron and organomanganese complexes using the reformatsky reagent Tetrahedron Letters. 24: 2465-2468. DOI: 10.1016/S0040-4039(00)81956-5 |
0.306 |
|
| 1983 |
Pearson AJ, Richards IC. Preparation and reactivity of ν6-veratrolemanganese tricarbonyl tetrafluoroborate Journal of Organometallic Chemistry. 258. DOI: 10.1016/S0022-328X(00)99267-2 |
0.516 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
PEARSON AJ, KOLE SL, CHEN B. ChemInform Abstract: ORGANOIRON COMPLEXES IN ORGANIC SYNTHESIS. 30. APPROACH TO STEREOCHEMICALLY DEFINED CYCLOHEPTADIENE DERIVATIVES USING ORGANOIRON CHEMISTRY Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341301 |
0.304 |
|
| 1983 |
Pearson AJ, Rees DC, Thornber CW. Organoiron Complexes In Organic Synthesis. Part 26. Synthetic Approaches To C-18 Oxygenated Aspidosperma Alkaloids Via Organoiron Complexes Cheminform. 14. DOI: 10.1002/Chin.198324344 |
0.394 |
|
| 1982 |
Pearson AJ, Chandler M. Organoiron complexes in organic synthesis. Part 24.<sup>1</sup> Studies in the synthesis and reactivity of 6-exo-substituted cyclohexadienylium(Tricarbonyl) iron salts Journal of the Chemical Society, Perkin Transactions 1. 2641-2646. DOI: 10.1039/P19820002641 |
0.496 |
|
| 1982 |
Pearson AJ, Heywood GC, Chandler M. Organoiron complexes in organic synthesis. Part 23. New strategies for steroid and aphidicolane synthesis Journal of the Chemical Society, Perkin Transactions 1. 2631-2639. DOI: 10.1039/P19820002631 |
0.47 |
|
| 1982 |
Pearson AJ, Rees DC. Total synthesis of (±)-limaspermine and formal synthesis of (±)-aspidospermine using organoiron complexes Journal of the Chemical Society-Perkin Transactions 1. 2467-2476. DOI: 10.1039/P19820002467 |
0.352 |
|
| 1982 |
Pearson AJ, Ham P, Ong CW, Perrior TR, Rees DC. Organoiron complexes in organic synthesis. Part 21. Methods for controlling the regioselectivity of nucleophile addition to tricarbonyl(cyclohexadienylium)iron complexes Journal of the Chemical Society-Perkin Transactions 1. 13: 1527-1534. DOI: 10.1039/P19820001527 |
0.516 |
|
| 1982 |
Pearson AJ, Ham P, Rees DC. Organoiron complexes in organic synthesis. Part 18. Spiroannelation reactions of some bifunctional tricarbonyl(cyclohexadienyl)iron hexafluorophosphate salts Journal of the Chemical Society-Perkin Transactions 1. 13: 489-497. DOI: 10.1039/P19820000489 |
0.519 |
|
| 1982 |
Pearson AJ, Richards IC, Gardner DV. A convergent approach to the synthesis of (±)-O-methyljoubertiamine using organoiron complexes Journal of the Chemical Society, Chemical Communications. 807-809. DOI: 10.1039/C39820000807 |
0.335 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/Jo00140A044 |
0.434 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| 1982 |
Pearson AJ, Ong CW. Organoiron complexes in organic synthesis. 25. Complete stereocontrol in the synthesis of 4,4,5-trisubstituted cyclohexenones The Journal of Organic Chemistry. 47: 3780-3782. DOI: 10.1021/jo00140a044 |
0.322 |
|
| Show low-probability matches. |
