| Year |
Citation |
Score |
| 2014 |
Maddani MR, Fiaud JC, Kagan HB. Stoichiometric Kinetic Resolution Reactions Separation of Enantiomers: Synthetic Methods. 13-74. DOI: 10.1002/9783527650880.ch2 |
0.721 |
|
| 2013 |
Gopalaiah K, Kagan HB. Recent developments in samarium diiodide promoted organic reactions. Chemical Record (New York, N.Y.). 13: 187-208. PMID 23468168 DOI: 10.1002/Tcr.201200028 |
0.3 |
|
| 2012 |
Haleema S, Sasi PV, Ibnusaud I, Polavarapu PL, Kagan HB. Enantiomerically pure compounds related to chiral hydroxy acids derived from renewable resources Rsc Advances. 2: 9257-9285. DOI: 10.1039/C2Ra21205F |
0.347 |
|
| 2012 |
Kagan HB. Chiral Ligands for Asymmetric Catalysis Asymmetric Synthesis. 1-39. DOI: 10.1002/Chin.198631351 |
0.384 |
|
| 2011 |
Anas S, Cordi A, Kagan HB. Enantioselective synthesis of 2-methyl indolines by palladium catalysed asymmetric C(sp3)-H activation/cyclisation. Chemical Communications (Cambridge, England). 47: 11483-5. PMID 21927738 DOI: 10.1039/C1Cc14292E |
0.429 |
|
| 2011 |
Gopalaiah K, Kagan HB. Use of nonfunctionalized enamides and enecarbamates in asymmetric synthesis. Chemical Reviews. 111: 4599-657. PMID 21568332 DOI: 10.1021/Cr100031F |
0.37 |
|
| 2011 |
Kumar RR, Haveli SD, Kagan HB. A mild one-pot method for conversion of various steroidal secondary alcohols into the corresponding olefins Synlett. 1709-1712. DOI: 10.1055/S-0030-1260803 |
0.582 |
|
| 2011 |
Kagan HB, Gopalaiah K. Early history of asymmetric synthesis: Who are the scientists who set up the basic principles and the first experiments? New Journal of Chemistry. 35: 1933-1937. DOI: 10.1039/C1Nj20216B |
0.357 |
|
| 2010 |
Kagan HB, Fiaud JC, Hoornaert C, Meyer D, Poulin JC. Synthesis of new chiral phosphines for asymmetric catalysis Bulletin Des SociéTéS Chimiques Belges. 88: 923-931. DOI: 10.1002/Bscb.19790881113 |
0.396 |
|
| 2010 |
Kumar RR, Kagan HB. Regioselective Reactions on a Chiral Substrate Controlled by the Configuration of a Chiral Catalyst Advanced Synthesis & Catalysis. 352: 231-242. DOI: 10.1002/Adsc.200900822 |
0.654 |
|
| 2009 |
Satyanarayana T, Abraham S, Kagan HB. Nonlinear effects in asymmetric catalysis. Angewandte Chemie (International Ed. in English). 48: 456-94. PMID 19115268 DOI: 10.1002/Anie.200705241 |
0.431 |
|
| 2009 |
Delamare M, Belot S, Caille JC, Martinet F, Kagan HB, Henryon V. A new titanate/(+)-(1R,2S)-cis-1-amino-2-indanol system for the asymmetric synthesis of (S)-tenatoprazole Tetrahedron Letters. 50: 1702-1704. DOI: 10.1016/J.Tetlet.2009.01.111 |
0.388 |
|
| 2009 |
Anas S, Kagan HB. Routes toward enantiopure 2-substituted indolines: an overview Tetrahedron Asymmetry. 20: 2193-2199. DOI: 10.1016/J.Tetasy.2009.08.008 |
0.423 |
|
| 2009 |
Belokon YN, Chusov D, Peregudov AS, Yashkina LV, Timofeeva GI, Maleev VI, North M, Kagan HB. Asymmetric meso-epoxide ring-opening with trimethylsilyl cyanide promoted by chiral binuclear complexes of titanium. Dichotomy of C-C versus C-N bond formation Advanced Synthesis and Catalysis. 351: 3157-3167. DOI: 10.1002/Adsc.200900523 |
0.41 |
|
| 2009 |
Kagan HB. Asymmetric Synthesis of Chiral Sulfoxides Organosulfur Chemistry in Asymmetric Synthesis. 1-29. DOI: 10.1002/9783527623235.ch1 |
0.354 |
|
| 2008 |
Tsukamoto M, Gopalaiah K, Kagan HB. Equilibrium of homochiral oligomerization of a mixture of enantiomers. Its relevance to nonlinear effects in asymmetric catalysis. The Journal of Physical Chemistry. B. 112: 15361-8. PMID 19006277 DOI: 10.1021/Jp8058917 |
0.387 |
|
| 2008 |
Gopalaiah K, Kagan HB. Use of samarium diiodide in the field of asymmetric synthesis New Journal of Chemistry. 32: 607-637. DOI: 10.1039/B718330P |
0.401 |
|
| 2008 |
Fan CA, Ferber B, Kagan HB, Lafon O, Lesot P. Two aspects of the desymmetrization of selected prochiral aromatic or vinylic dihalides: enantioselective halogen-lithium exchange and prochiral recognition in chiral liquid crystals Tetrahedron Asymmetry. 19: 2666-2677. DOI: 10.1016/J.Tetasy.2008.12.003 |
0.438 |
|
| 2007 |
Lafon O, Lesot P, Fan CA, Kagan HB. Analysis of intramolecular dynamic processes in enantiomeric diaryl atropisomers and related derivatives by 2H NMR spectroscopy in polypeptide liquid crystals. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 3772-86. PMID 17225229 DOI: 10.1002/Chem.200601284 |
0.314 |
|
| 2007 |
Satyanarayana T, Ferber B, Kagan HB. Asymmetric amplification in catalysis by trans-1,2-diaminocyclohexane bistriflamide. Organic Letters. 9: 251-3. PMID 17217277 DOI: 10.1021/Ol062653B |
0.337 |
|
| 2007 |
Satyanarayana T, Kagan HB. Amplification of the enantiomeric excess of a compound in kinetic resolution by a racemic reagent Tetrahedron. 63: 6415-6422. DOI: 10.1016/J.Tet.2007.03.077 |
0.371 |
|
| 2007 |
Kumar RS, Perumal S, Kagan HB, Guillot R. 1,3-Dipolar cycloaddition of nitrile oxides to (R)-1-(1-phenylethyl)-3-[(E)-arylmethylidene]tetrahydro-4(1H)-pyridinones: synthesis of enantiomerically pure spiro heterocycles Tetrahedron Asymmetry. 18: 170-180. DOI: 10.1002/CHIN.200725091 |
0.576 |
|
| 2007 |
Ferber B, Kagan HB. Metallocene sulfoxides as precursors of metallocenes with planar chirality Advanced Synthesis and Catalysis. 349: 493-507. DOI: 10.1002/Adsc.200600639 |
0.429 |
|
| 2007 |
Kagan HB. Organocatalytic Enantioselective Reduction of Olefins, Ketones, and Imines Enantioselective Organocatalysis: Reactions and Experimental Procedures. 391-401. DOI: 10.1002/9783527610945.ch11 |
0.375 |
|
| 2006 |
Satyanarayana T, Kagan HB. Asymmetric amplification by kinetic resolution using a racemic reagent: example in amine acetylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 5785-9. PMID 16703657 DOI: 10.1002/Chem.200600026 |
0.439 |
|
| 2006 |
Lesot P, Lafon O, Kagan HB, Fan CA. Study of molecular rotational isomerism using deuterium NMR in chiral oriented solvents. Chemical Communications (Cambridge, England). 389-91. PMID 16493808 DOI: 10.1039/B514694A |
0.331 |
|
| 2006 |
Kumar RR, Perumal S, Kagan HB, Guillot R. Chemo-, regio- and stereoselective 1,3-dipolar cycloaddition of C-aryl-N-phenylnitrones over 3,5-bis(arylidene)-1-methylpiperidin-4-ones: synthesis of highly substituted novel spiro-isoxazolidines Tetrahedron. 62: 12380-12391. DOI: 10.1016/J.Tet.2006.09.106 |
0.717 |
|
| 2006 |
Kagan HB. Twenty five years of organic chemistry with diiodosamarium Journal of Alloys and Compounds. 408: 421-426. DOI: 10.1016/J.Jallcom.2004.11.090 |
0.349 |
|
| 2005 |
Satyanarayana T, Kagan HB. The multi-substrate screening of asymmetric catalysts Advanced Synthesis and Catalysis. 347: 737-748. DOI: 10.1002/Adsc.200505057 |
0.416 |
|
| 2004 |
Belokon YN, North M, Maleev VI, Voskoboev NV, Moskalenko MA, Peregudov AS, Dmitriev AV, Ikonnikov NS, Kagan HB. In situ formation of a heterobimetallic chiral [(salen)Ti(IV)]/[(salen)V(V)] catalyst for the asymmetric addition of TMSCN to benzaldehyde. Angewandte Chemie (International Ed. in English). 43: 4085-9. PMID 15300702 DOI: 10.1002/Anie.200454031 |
0.35 |
|
| 2003 |
Belokon YN, Bespalova NB, Churkina TD, Císarová I, Ezernitskaya MG, Harutyunyan SR, Hrdina R, Kagan HB, Kocovský P, Kochetkov KA, Larionov OV, Lyssenko KA, North M, Polásek M, Peregudov AS, et al. Synthesis of alpha-amino acids via asymmetric phase transfer-catalyzed alkylation of achiral nickel(II) complexes of glycine-derived Schiff bases. Journal of the American Chemical Society. 125: 12860-71. PMID 14558835 DOI: 10.1021/Ja035465E |
0.415 |
|
| 2003 |
Lagasse F, Tsukamoto M, Welch CJ, Kagan HB. Is it possible to estimate the enantioselectivity of a chiral catalyst from its racemic mixture? Journal of the American Chemical Society. 125: 7490-1. PMID 12812469 DOI: 10.1021/Ja0300315 |
0.409 |
|
| 2003 |
Brunner H, Kagan HB, Kreutzer G. Asymmetric catalysis. Part 153: Metal-catalysed enantioselective α-ketol rearrangement Tetrahedron Asymmetry. 14: 2177-2187. DOI: 10.1016/S0957-4166(03)00433-6 |
0.317 |
|
| 2002 |
Kagan HB. Introduction: Frontiers in lanthanide chemistry Chemical Reviews. 102: 1805-1806. DOI: 10.1021/Cr020014I |
0.302 |
|
| 2002 |
Luukas TO, Fenwick DR, Kagan HB. Presence or absence of a nonlinear effect according to the asymmetric catalyst preparation in the alkylation of benzaldehyde Comptes Rendus Chimie. 5: 487-491. DOI: 10.1016/S1631-0748(02)01402-9 |
0.337 |
|
| 2002 |
Norsikian S, Holmes I, Lagasse F, Kagan HB. A one-pot esterification of chiral O-trimethylsilyl-cyanohydrins with retention of stereochemistry Tetrahedron Letters. 43: 5715-5717. DOI: 10.1016/S0040-4039(02)01200-5 |
0.365 |
|
| 2002 |
Tsukamoto M, Kagan HB. Recent Advances in the Measurement of Enantiomeric Excesses Advanced Synthesis and Catalysis. 344: 453-463. DOI: 10.1002/1615-4169(200207)344:5<453::Aid-Adsc453>3.0.Co;2-U |
0.322 |
|
| 2001 |
Belokon YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Larionov OV, Harutyunyan SR, Vyskocil S, North M, Kagan HB. Highly Efficient Catalytic Synthesis of alpha-Amino Acids under Phase-Transfer Conditions with a Novel Catalyst/Substrate Pair This work was supported by an ISTC (grant A-356), by the Russian Foundation for Basic Research (Project No 99-03-32970), the Grant Agency of the Czech Republic (Grant No. 203/00/0601), and also by the Grant Agency of Charles University (Grant No. 18/98). We thank Prof. Pavel Kocovský for encouragement and proofreading the manuscript. Angewandte Chemie (International Ed. in English). 40: 1948-1951. PMID 11385682 DOI: 10.1002/1521-3773(20010518)40:10<1948::Aid-Anie1948>3.0.Co;2-O |
0.401 |
|
| 2001 |
Dorizon P, Martin C, Daran JC, Fiaud JC, Kagan HB. A practical kinetic resolution of 4-acetyl[2.2]paracyclophane Tetrahedron Asymmetry. 12: 2625-2630. DOI: 10.1016/S0957-4166(01)00452-9 |
0.342 |
|
| 2001 |
Brunner H, Kagan HB, Kreutzer G. Asymmetric catalysis. Part 137: Nickel catalysed enantioselective α-ketol rearrangement of 1-benzoylcycloalkanols Tetrahedron Asymmetry. 12: 497-499. DOI: 10.1016/S0957-4166(01)00045-3 |
0.403 |
|
| 2001 |
Kagan HB. Various aspects of the reaction of a chiral catalyst or reagent with a racemic or enantiopure substrate Tetrahedron. 57: 2449-2468. DOI: 10.1016/S0040-4020(01)00065-5 |
0.453 |
|
| 2001 |
Kagan HB. Practical Consequences of Non-Linear Effects in Asymmetric Synthesis Advanced Synthesis and Catalysis. 343: 227-233. DOI: 10.1002/1615-4169(20010330)343:3<227::Aid-Adsc227>3.0.Co;2-X |
0.386 |
|
| 2000 |
Belokon YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Chesnokov AA, Larionov OV, Singh I, Parmar VS, Vyskocil S, Kagan HB. Asymmetric PTC C-alkylation catalyzed by chiral derivatives of tartaric acid and aminophenols. Synthesis Of (R)- and (S)-alpha-methyl amino acids The Journal of Organic Chemistry. 65: 7041-8. PMID 11031026 DOI: 10.1021/Jo000719P |
0.44 |
|
| 2000 |
Lagasse F, Kagan HB. Chiral monophosphines as ligands for asymmetric organometallic catalysis. Chemical & Pharmaceutical Bulletin. 48: 315-24. PMID 10726849 DOI: 10.1248/Cpb.48.315 |
0.359 |
|
| 2000 |
Girard C, Kagan HB. On diastereomeric perturbations Canadian Journal of Chemistry. 78: 816-828. DOI: 10.1139/V00-077 |
0.418 |
|
| 2000 |
Guillaneux D, Martiny L, Kagan HB. Diferrocenylphosphine: A facile synthesis and its use to prepare chiral phosphines Collection of Czechoslovak Chemical Communications. 65: 717-728. DOI: 10.1135/Cccc20000717 |
0.436 |
|
| 2000 |
Holmes IP, Kagan HB. The asymmetric addition of trimethylsilylcyanide to aldehydes catalysed by anionic chiral nucleophiles. Part 2 Tetrahedron Letters. 41: 7457-7460. DOI: 10.1016/S0040-4039(00)01276-4 |
0.471 |
|
| 2000 |
Argouarch G, Samuel O, Riant O, Daran J, Kagan HB. A New Class of Ferrocene‐Based l,2‐Bis(phosphanes) Possessing only Planar Chirality European Journal of Organic Chemistry. 2000: 2893-2899. DOI: 10.1002/1099-0690(200008)2000:16<2893::Aid-Ejoc2893>3.0.Co;2-D |
0.656 |
|
| 2000 |
Argouarch G, Samuel O, Kagan HB. Synthesis of some ferrocene-based 1,3-bis(phosphanes) with planar chirality as the sole source of chirality European Journal of Organic Chemistry. 2885-2891. DOI: 10.1002/1099-0690(200008)2000:16<2885::Aid-Ejoc2885>3.0.Co;2-3 |
0.474 |
|
| 2000 |
Holmes IP, Kagan HB. The asymmetric addition of trimethylsilylcyanide to aldehydes catalysed by anionic chiral nucleophiles. Part 1 Tetrahedron Letters. 41: 7453-7456. |
0.376 |
|
| 1999 |
Luukas TO, Girard C, Fenwick DR, Kagan HB. Kinetic resolution when the chiral auxiliary is not enantiomerically pure: Normal and abnormal behavior Journal of the American Chemical Society. 121: 9299-9306. DOI: 10.1021/Ja990793T |
0.414 |
|
| 1999 |
Belokon' YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Vyskocil S, Kagan HB. Enantiomerically enriched (R)- and (S)-α-methylphenylalanine via asymmetric PTC C-alkylation catalysed by NOBIN Tetrahedron Asymmetry. 10: 1723-1728. DOI: 10.1016/S0957-4166(99)00185-8 |
0.363 |
|
| 1998 |
Girard C, Kagan HB. Nonlinear Effects in Asymmetric Synthesis and Stereoselective Reactions: Ten Years of Investigation. Angewandte Chemie (International Ed. in English). 37: 2922-2959. PMID 29711141 DOI: 10.1002/(Sici)1521-3773(19981116)37:21<2922::Aid-Anie2922>3.0.Co;2-1 |
0.431 |
|
| 1998 |
Riant O, Argouarch G, Guillaneux D, Samuel O, Kagan HB. A Straightforward Asymmetric Synthesis of Enantiopure 1,2-Disubstituted Ferrocenes Journal of Organic Chemistry. 63: 3511-3514. DOI: 10.1021/Jo9800614 |
0.654 |
|
| 1998 |
Fiaud JC, Mazé F, Kagan HB. Chiral hydroxythiols as catalysts for enantioselective borane ketone reductions Tetrahedron Asymmetry. 9: 3647-3655. DOI: 10.1016/S0957-4166(98)00376-0 |
0.43 |
|
| 1998 |
Brunel JM, Luukas TO, Kagan HB. Nonlinear effects as 'indicators' in the tuning of asymmetric catalysts Tetrahedron Asymmetry. 9: 1941-1946. DOI: 10.1016/S0957-4166(98)00168-2 |
0.362 |
|
| 1998 |
Belokon' YN, Kochetkov KA, Churkina TD, Ikonnikov NS, Chesnokov AA, Larionov OV, Parmár VS, Kumar R, Kagan HB. Asymmetric PTC C-alkylation mediated by TADDOL - Novel route to enantiomerically enriched α-alkyl-α-amino acids Tetrahedron Asymmetry. 9: 851-857. DOI: 10.1016/S0957-4166(98)00044-5 |
0.342 |
|
| 1998 |
Hamann-Gaudinet B, Namy JL, Kagan HB. Organosamariums: Preparation using diiodosamarium and reactivity in tetrahydropyran Journal of Organometallic Chemistry. 567: 39-47. DOI: 10.1016/S0022-328X(98)00666-4 |
0.39 |
|
| 1998 |
Kagan HB. New screening methodologies or combinatorial chemistry applied to asymmetric catalysts Journal of Organometallic Chemistry. 567: 3-6. DOI: 10.1016/S0022-328X(98)00660-3 |
0.398 |
|
| 1998 |
Gao X, Kagan HB. One-pot multi-substrate screening in asymmetric catalysis Chirality. 10: 120-124. DOI: 10.1002/Chir.19 |
0.376 |
|
| 1997 |
Schiffers R, Kagan HB. Asymmetric Catalytic Reduction of Ketones with Hypervalent Trialkoxysilanes Synlett. 1997: 1175-1178. DOI: 10.1055/S-1997-982 |
0.391 |
|
| 1997 |
Riant O, Samuel O, Flessner T, Taudien S, Kagan HB. An Efficient Asymmetric Synthesis of 2-Substituted Ferrocenecarboxaldehydes Journal of Organic Chemistry. 62: 6733-6745. DOI: 10.1021/Jo970075U |
0.647 |
|
| 1997 |
Machrouhi F, Namy JL, Kagan HB. Nucleophilic acylation of esters by acid chlorides mediated by samarium diiodide: Formation and use of samarium enediolates. Tetrahedron Letters. 38: 7183-7186. DOI: 10.1016/S0040-4039(97)01727-9 |
0.359 |
|
| 1997 |
Hamann-Gaudinet B, Namy JL, Kagan HB. Generation and reactivity of allylic and benzylic samarium compounds using diiodosamarium in tetrahydropyran Tetrahedron Letters. 38: 6585-6588. DOI: 10.1016/S0040-4039(97)01506-2 |
0.328 |
|
| 1997 |
Brunner A, Taudien S, Riant O, Kagan HB. Stereoselective synthesis of some chiral α-ferrocenyl carbenium ions Chirality. 9: 478-486. DOI: 10.1002/(Sici)1520-636X(1997)9:5/6<478::Aid-Chir14>3.0.Co;2-L |
0.64 |
|
| 1996 |
Kagan HB, Diter P, Gref A, Guillaneux D, Masson-Szymczak A, Rebière F, Riant O, Samuel O, Taudien S. Towards new ferrocenyl ligands for asymmetric catalysis Pure and Applied Chemistry. 68: 29-36. DOI: 10.1351/Pac199668010029 |
0.663 |
|
| 1996 |
Brunel JM, Kagan HB. Catalytic Asymmetric Oxidation of Sulfides with High Enantioselectivities Synlett. 1996: 404-406. DOI: 10.1055/S-1996-5413 |
0.343 |
|
| 1996 |
Hamann B, Namy JL, Kagan HB. Preparation and reactions of samarium diiodide in nitriles Tetrahedron. 52: 14225-14234. DOI: 10.1016/0040-4020(96)00861-7 |
0.357 |
|
| 1996 |
Masson-Szymczak A, Riant O, Gref A, Kagan HB. Asymmetric synthesis of a chiral tetradentate ligand based on a bis[diphenylphosphinoferrocenyl] moiety. Electrochemical behavior of free ligand and its ruii and cui complexes Journal of Organometallic Chemistry. 511: 193-197. DOI: 10.1016/0022-328X(95)05968-U |
0.625 |
|
| 1995 |
Brunel JM, Diter P, Duetsch M, Kagan HB. Highly enantioselective oxidation of sulfides mediated by a chiral titanium complex Journal of Organic Chemistry. 60: 8086-8088. DOI: 10.1021/Jo00129A060 |
0.371 |
|
| 1995 |
Guillaneux D, Kagan HB. High yield synthesis of monosubstituted ferrocenes Journal of Organic Chemistry. 60: 2502-2505. DOI: 10.1021/Jo00113A033 |
0.383 |
|
| 1995 |
Zhang SY, Girard C, Kagan HB. Nonlinear effects involving two competing pseudo-enantiomeric catalysts: Example in asymmetric dihydroxylation of olefins Tetrahedron: Asymmetry. 6: 2637-2640. DOI: 10.1016/0957-4166(95)00344-O |
0.37 |
|
| 1995 |
Dubois L, Fiaud JC, Kagan HB. Enantioselective borane reduction of acetophenone catalysed by oxazaborolidines derived from chiral diethanolamines Tetrahedron: Asymmetry. 6: 1097-1104. DOI: 10.1016/0957-4166(95)00134-B |
0.433 |
|
| 1995 |
Kless A, Kadyrov R, Börner A, Holz J, Kagan HB. A new chiral multidentate ligand for asymmetric catalysis Tetrahedron Letters. 36: 4601-4602. DOI: 10.1016/0040-4039(95)00844-3 |
0.405 |
|
| 1995 |
Taudien S, Riant O, Kagan HB. Synthesis of chiral carbocations linked to a ferrocene unit Tetrahedron Letters. 36: 3513-3516. DOI: 10.1016/0040-4039(95)00531-G |
0.687 |
|
| 1995 |
Dubois L, Fiaud JC, Kagan HB. Synthesis of chiral lithium diatkoxyaminoborohydrides Tetrahedron. 51: 3803-3812. DOI: 10.1016/0040-4020(95)00101-D |
0.429 |
|
| 1995 |
Dallemer F, Collin J, Kagan HB. Synthesis of tertiary phosphine oxides mediated by SmCp2 or Sml2 Applied Organometallic Chemistry. 9: 431-435. DOI: 10.1002/Aoc.590090510 |
0.401 |
|
| 1994 |
Diter P, Taudien S, Samuel O, Kagan HB. Enantiomeric enrichment of sulfoxides by preparative flash chromatography on an achiral phase Journal of Organic Chemistry. 59: 370-373. DOI: 10.1021/Jo00081A015 |
0.34 |
|
| 1994 |
Börner A, Ward J, Ruth W, Holz J, Kless A, Heller D, Kagan HB. Synthesis and catalytic properties of an acyclic analogue of hydroxy norphos Tetrahedron. 50: 10419-10430. DOI: 10.1016/S0040-4020(01)89582-X |
0.433 |
|
| 1994 |
Riant O, Kagan HB, Ricard L. Asymmetric base-catalyzed cycloaddition between anthrone and some dienophiles Tetrahedron. 50: 4543-4554. DOI: 10.1016/S0040-4020(01)89385-6 |
0.633 |
|
| 1994 |
Diter P, Samuel O, Taudien S, Kagan HB. Highly enantioselective oxidation of ferrocenyl sulfides Tetrahedron: Asymmetry. 5: 549-552. DOI: 10.1016/0957-4166(94)80015-4 |
0.358 |
|
| 1994 |
Namy JL, Colomb M, Kagan HB. Samarium diiodide in tetrahydropyran : Preparation and some reactions in organic chemistry Tetrahedron Letters. 35: 1723-1726. DOI: 10.1016/0040-4039(94)88329-7 |
0.372 |
|
| 1993 |
Börner A, Holz J, Ward J, Kagan HB. Concise synthesis of enantiomerically pure cis- and trans-3-(diphenylphosphino)-4-hydroxytetrahydrofurans Journal of Organic Chemistry. 58: 6814-6817. DOI: 10.1021/Jo00076A050 |
0.339 |
|
| 1993 |
Riant O, Samuel O, Kagan HB. A general asymmetric synthesis of ferrocenes with planar chirality Journal of the American Chemical Society. 115: 5835-5836. DOI: 10.1021/Ja00066A066 |
0.662 |
|
| 1993 |
Börner A, Ward J, Kortus K, Kagan HB. A boron analog of diop: synthesis and properties Tetrahedron: Asymmetry. 4: 2219-2228. DOI: 10.1016/S0957-4166(00)80072-5 |
0.374 |
|
| 1993 |
Lebrun A, Namy JL, Kagan HB. Samarium dibromide an efficient reagent for the Pinacol coupling reactions Tetrahedron Letters. 34: 2311-2314. DOI: 10.1016/S0040-4039(00)77601-5 |
0.354 |
|
| 1993 |
Börner A, Holz J, Kagan HB. New chiral building blocks and their application to the construction of chiral aminoalcohols: Enantiomerically pure cis- and trans-3-mesyloxy-4-hydroxy tetrahydrofurans Tetrahedron Letters. 34: 5273-5276. DOI: 10.1016/S0040-4039(00)73971-2 |
0.429 |
|
| 1993 |
Kagan HB, Collin J, Namy JL, Bied C, Dallemer F, Lebrun A. Divalent lanthanides in organic chemistry Journal of Alloys and Compounds. 192: 191-196. DOI: 10.1016/0925-8388(93)90228-F |
0.307 |
|
| 1993 |
Rebière F, Riant O, Ricard L, Kagan HB. Asymmetric synthesis and highly diastereoselective ortho-lithiation of ferrocenyl sulfoxides. Application to the synthesis of ferrocenyl derivatives with planar chirality Angewandte Chemie (International Edition in English). 32: 568-570. DOI: 10.1002/Anie.199305681 |
0.62 |
|
| 1993 |
Rebière F, Riant O, Ricard L, Kagan HB. Asymmetrische Synthese und hoch diastereoselektive ortho‐Lithiierung von Ferrocenylsulfoxiden; Anwendung in der Synthese von Planar‐chiralen Ferrocenylderivaten Angewandte Chemie. 105: 644-646. DOI: 10.1002/Ange.19931050446 |
0.601 |
|
| 1992 |
Namy JL, Collin J, Bied C, Kagan HB. Organosamariums from Reaction of Alkyl Halides with Samarium(II) Derivatives Synlett. 1992: 733-734. DOI: 10.1055/S-1992-21472 |
0.344 |
|
| 1992 |
Kagan HB, Riant O. Catalytic asymmetric Diels-Alder reactions Chemical Reviews. 92: 1007-1019. DOI: 10.1021/Cr00013A013 |
0.626 |
|
| 1992 |
Ronan B, Kagan HB. Highly enantioselective synthesis of a Corey prostaglandin intermediate Tetrahedron: Asymmetry. 3: 115-122. DOI: 10.1016/S0957-4166(00)82318-6 |
0.395 |
|
| 1992 |
Ward J, Börner A, Kagan HB. Synthesis of 6-endo-hydroxy norphos, a potential ligand for construction of chiral bimetallic catalysts Tetrahedron: Asymmetry. 3: 849-852. DOI: 10.1016/S0957-4166(00)82181-3 |
0.406 |
|
| 1992 |
Hammadi A, Nuzillard JM, Poulin JC, Kagan HB. Diastereoselective hydrogenation of monodehydro enkephalins controlled by chiral rhodium catalysts Tetrahedron: Asymmetry. 3: 1247-1262. DOI: 10.1016/S0957-4166(00)82083-2 |
0.594 |
|
| 1992 |
Collin J, Namy JL, Jones G, Kagan HB. Reactions of protected amino acid chlorides mediated by SmI2 Tetrahedron Letters. 33: 2973-2976. DOI: 10.1016/S0040-4039(00)79575-X |
0.367 |
|
| 1992 |
Bied C, Collin J, Kagan HB. Synthesis and reactivity of benzylic and allylic samarium compounds Tetrahedron. 48: 3877-3890. DOI: 10.1016/S0040-4020(01)88468-4 |
0.437 |
|
| 1991 |
Kagan HB, Rebeere F, Samuel O. New approaches for asymmetric synthesis of sulfoxides Phosphorus, Sulfur, and Silicon and the Related Elements. 58: 89-110. DOI: 10.1080/10426509108040627 |
0.41 |
|
| 1991 |
Rebiere F, Samuel O, Ricard L, Kagan HB. A general route to enantiomerically pure sulfoxides from a chiral sulfite Journal of Organic Chemistry. 56: 5991-5999. DOI: 10.1021/Jo00021A008 |
0.402 |
|
| 1991 |
Collin J, Namy JL, Dallemer F, Kagan HB. Synthesis Of Alpha -Ketols Mediated By Divalent Samarium Compounds Journal of Organic Chemistry. 56: 3118-3122. DOI: 10.1021/Jo00009A035 |
0.39 |
|
| 1991 |
Ronan B, Kagan HB. Highly diastereoselective Diels-Alder reactions with (R)-ethoxy p-tolyl vinyl sulfonium tetrafluoroborate Tetrahedron: Asymmetry. 2: 75-90. DOI: 10.1016/S0957-4166(00)82159-X |
0.373 |
|
| 1991 |
Lebrun A, Namy JL, Kagan HB. A new preparation of lanthanide alkoxide, and some applications in catalysis Tetrahedron Letters. 32: 2355-2358. DOI: 10.1016/S0040-4039(00)79922-9 |
0.441 |
|
| 1991 |
Kagan HB, Tahar M, Fiaud JC. 2-Hydroxyalkyl diphenylphosphines: Biocatalytic resolution and use as ligands for transition-metal catalysts Tetrahedron Letters. 32: 5959-5962. DOI: 10.1016/S0040-4039(00)79437-8 |
0.348 |
|
| 1991 |
Collin J, Bied C, Kagan HB. Synthesis and reactivity of allyl samarium complexes Tetrahedron Letters. 32: 629-630. DOI: 10.1016/S0040-4039(00)74845-3 |
0.45 |
|
| 1991 |
Sasaki M, Collin J, Kagan HB. Reactions of P_CI compounds in presence of SMI2 Tetrahedron Letters. 32: 2493-2496. DOI: 10.1016/S0040-4039(00)74363-2 |
0.303 |
|
| 1991 |
Chauvin R, Kagan HB. Solid angle as steric parameter of acyclic saturated groups Chirality. 3: 242-253. DOI: 10.1002/Chir.530030406 |
0.542 |
|
| 1990 |
Kagan HB, Rebiere F. Some Routes to Chiral Sulfoxides with Very High Enantiomeric Excesses Synlett. 1990: 643-650. DOI: 10.1055/S-1990-21198 |
0.398 |
|
| 1990 |
Rebiere F, Samuel O, Kagan HB. A convenient method for the preparation of monolithioferrocene Tetrahedron Letters. 31: 3121-3124. DOI: 10.1016/S0040-4039(00)94710-5 |
0.377 |
|
| 1990 |
Rebiere F, Riant O, Kagan HB. Asymmetric Diels-Alder reaction catalysed by some chiral Lewis acids Tetrahedron: Asymmetry. 1: 199-214. DOI: 10.1016/0957-4166(90)90014-2 |
0.659 |
|
| 1990 |
Baldenius KU, Kagan HB. Synthesis of new optically active sulfoxides with chelating properties Tetrahedron: Asymmetry. 1: 593-596. DOI: 10.1016/0957-4166(90)80010-V |
0.371 |
|
| 1989 |
Rebiere F, Kagan HB. An efficient route to chiral t-butyl sulfoxides Tetrahedron Letters. 30: 3659-3662. DOI: 10.1016/S0040-4039(01)80475-5 |
0.463 |
|
| 1989 |
Collin J, Dallemer F, Namy JL, Kagan HB. Reductive couplings of acid chlorides mediated by SmI2 Tetrahedron Letters. 30: 7407-7410. DOI: 10.1016/S0040-4039(00)70710-6 |
0.342 |
|
| 1989 |
Riant O, Kagan HB. Asymmetric Diels-Alder reaction catalyzed by chiral bases Tetrahedron Letters. 30: 7403-7406. DOI: 10.1016/S0040-4039(00)70709-X |
0.662 |
|
| 1989 |
Schurig V, Hintzer K, Leyrer U, Mark C, Pitchen P, Kagan HB. Enantioselective epoxidation of unfunctionalized simple olefins by non-racemic molybdenum(VI)(oxo-diperoxo) complexes Journal of Organometallic Chemistry. 370: 81-96. DOI: 10.1016/0022-328X(89)87277-8 |
0.43 |
|
| 1989 |
Samuel O, Ronan B, Kagan HB. Asymmetric oxidation of some 1,3-dithianes in presence of chiral titanium complexes Journal of Organometallic Chemistry. 370: 43-50. DOI: 10.1016/0022-328X(89)87273-0 |
0.37 |
|
| 1988 |
Kagan HB, Sasaki M, Collin J. Organic chemistry with lanthanides Pure and Applied Chemistry. 60: 1725-1730. DOI: 10.1351/Pac198860111725 |
0.327 |
|
| 1988 |
Sasaki M, Collin J, Kagan HB. Double cyclization of allyloxybenzoic acid chlorides mediated by samarium diiodide giving cyclopropanols Tetrahedron Letters. 29: 6105-6106. DOI: 10.1016/S0040-4039(00)82276-5 |
0.333 |
|
| 1988 |
Ronan B, Marchalin S, Samuel O, Kagan HB. Asymmetric additions of α-sulfoxide carbanion on imines Tetrahedron Letters. 29: 6101-6104. DOI: 10.1016/S0040-4039(00)82275-3 |
0.367 |
|
| 1988 |
Sasaki M, Collin J, Kagan HB. Synthesis of 1,2-glycol monoethers utilizing decarbonylation ofα-alkoxyacid chlorides mediated by samarium diiodide Tetrahedron Letters. 29: 4847-4850. DOI: 10.1016/S0040-4039(00)80624-3 |
0.306 |
|
| 1987 |
Vougioukas AE, Kagan HB. Oxirane ring opening reactions with thiols catalyzed by lanthanide complexes Tetrahedron Letters. 28: 6065-6068. DOI: 10.1016/S0040-4039(00)96865-5 |
0.404 |
|
| 1987 |
Vougioukas AE, Kagan HB. Lanthanides as lewis-acid catalysts in aldol addition,cyanohydrin-forming and oxirane ring opening reactions Tetrahedron Letters. 28: 5513-5516. DOI: 10.1016/S0040-4039(00)96767-4 |
0.455 |
|
| 1987 |
Zhao SH, Samuel O, Kagan HB. Asymmetric oxidation of sulfides mediated by chiral titanium complexes : mechanistic and synthetic aspects Tetrahedron. 43: 5135-5144. DOI: 10.1016/S0040-4020(01)87689-4 |
0.384 |
|
| 1987 |
Namy JL, Collin J, Zhang J, Kagan HB. The evaluation of dicyclopentadienylsamarium as a reagent in organic synthesis Journal of Organometallic Chemistry. 328: 81-86. DOI: 10.1016/S0022-328X(00)99769-9 |
0.39 |
|
| 1987 |
Kagan HB. Lanthanide derivatives as reagents or catalysts for organic reactions Inorganica Chimica Acta. 140: 3-6. DOI: 10.1016/S0020-1693(00)81036-1 |
0.377 |
|
| 1986 |
Puchot C, Samuel O, Dunach E, Zhao S, Agami C, Kagan HB. Nonlinear effects in asymmetric synthesis. Examples in asymmetric oxidations and aldolization reactions. Journal of the American Chemical Society. 108: 2353-7. PMID 22175583 DOI: 10.1002/Chin.198634105 |
0.37 |
|
| 1986 |
Kagan HB. Synthesis Of Chiral Sulfoxides By Asymmetric Oxidation Phosphorus Sulfur and Silicon and the Related Elements. 27: 127-132. DOI: 10.1080/03086648608072765 |
0.425 |
|
| 1986 |
Nuzillard JM, Poulin JC, Kagan HB. Synthesis of a protected monodehydro Leu-enkephalin and its hydrogenation catalyzed by chiral rhodium complexes Tetrahedron Letters. 27: 2993-2996. DOI: 10.1016/S0040-4039(00)84699-7 |
0.63 |
|
| 1986 |
Charpin P, Duñach E, Kagan HB, Theobald FR. Formation of a crystalline molecular complex between a chiral sulfoxide and a chiral amide Tetrahedron Letters. 27: 2989-2992. DOI: 10.1016/S0040-4039(00)84698-5 |
0.385 |
|
| 1986 |
Prandi J, Kagan HB, Mimoun H. Epoxidation of isolated double bonds with 30% hydrogen peroxide catalyzed by pertungstate salts Tetrahedron Letters. 27: 2617-2620. DOI: 10.1016/S0040-4039(00)84599-2 |
0.342 |
|
| 1986 |
El-Baba S, Nuzillard JM, Poulin JC, Kagan HB. Asymmetric homogeneous reduction of dehydropeptides Tetrahedron. 42: 3851-3861. DOI: 10.1016/S0040-4020(01)87539-6 |
0.597 |
|
| 1986 |
EL-BABA S, NUZILLARD JM, POULIN JC, KAGAN HB. ChemInform Abstract: Asymmetric Homogeneous Reduction of Dehydropeptides. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198648309 |
0.533 |
|
| 1986 |
Collin J, Namy J-, Kagan HB. Samarium diiodide, an efficient catalyst precursor in some Oppenauer oxidations Cheminform. 10: 229-232. DOI: 10.1002/Chin.198646137 |
0.322 |
|
| 1986 |
Kagan HB. Asymmetric Synthesis. Herausgegeben von James D. Morrison. Academic Press, Orlando, FL, 1983–1985 Angewandte Chemie. 98: 655-658. DOI: 10.1002/Ange.19860980726 |
0.32 |
|
| 1985 |
Duñach E, Kagan HB. A simple chiral shift reagent for measurement of enantiomeric excesses of phosphine oxides Tetrahedron Letters. 26: 2649-2652. DOI: 10.1016/S0040-4039(00)98126-7 |
0.375 |
|
| 1985 |
Ouertani M, Collin J, Kagan HB. Ether formation from allylic alcohols catalyzed by samarium trichloride Tetrahedron. 41: 3689-3693. DOI: 10.1016/S0040-4020(01)91389-4 |
0.357 |
|
| 1985 |
Prandi J, Namy JL, Menoret G, Kagan HB. Selective catalyzed-rearrangement of terminal epoxides to methyl ketones Journal of Organometallic Chemistry. 285: 449-460. DOI: 10.1016/0022-328X(85)87389-7 |
0.407 |
|
| 1985 |
Kagan HB. 4f-Elements on Organic Synthesis Cheminform. 17: 49-76. DOI: 10.1007/978-94-009-5406-9_2 |
0.322 |
|
| 1985 |
Kagan HB, Duñach E, Nemecek C, Pitchen P, Samuel O, Zhao SH. A short route to chiral sulfoxides using titanium-mediated asymmetric oxidation Pure and Applied Chemistry. 57: 1911-1916. DOI: 10.1002/Chin.198615396 |
0.344 |
|
| 1984 |
Samuel O, Zhang SY, Kagan HB. Stereochemistry And Structure Of Phellanphos And Nopaphos, Two Chiral Diphosphines For Asymmetric Hydrogenation Phosphorus Sulfur and Silicon and the Related Elements. 21: 145-154. DOI: 10.1080/03086648408077650 |
0.364 |
|
| 1984 |
Namy JL, Souppe J, Collin J, Kagan HB. New preparations of lanthanide alkoxides and their catalytical activity in Meerwein-Ponndorf-Verley-Oppenauer reactions Journal of Organic Chemistry. 49: 2045-2049. DOI: 10.1021/Jo00185A053 |
0.376 |
|
| 1984 |
Deshmukh M, Duñach E, Juge S, Kagan HB. A convenient family of chiral shift reagents for measurement of enantiomeric excesses of sulfoxides Tetrahedron Letters. 25: 3467-3470. DOI: 10.1016/S0040-4039(01)91049-4 |
0.32 |
|
| 1984 |
Souppe J, Namy JL, Kagan HB. Reactions of acyl anions generated from acid chlorides and diiodosamarium Tetrahedron Letters. 25: 2869-2872. DOI: 10.1016/S0040-4039(01)81312-5 |
0.367 |
|
| 1984 |
El-Baba S, Poulin JC, Kagan HB. Partial resolution through chiral synthesis using a racemic mixture Tetrahedron. 40: 4275-4284. DOI: 10.1016/S0040-4020(01)98803-9 |
0.45 |
|
| 1983 |
Namy JL, Souppe J, Kagan HB. Efficient formation of pinacols from aldehydes or ketones mediated by samarium diiodide Tetrahedron Letters. 24: 765-766. DOI: 10.1016/S0040-4039(00)81521-X |
0.424 |
|
| 1983 |
Souppe J, Danon L, Namy JL, Kagan HB. Some organic reactions promoted by samarium diiodide Journal of Organometallic Chemistry. 250: 227-236. DOI: 10.1016/0022-328X(83)85053-0 |
0.383 |
|
| 1983 |
Ouertani M, Girard P, Kagan HB. The Easy Preparation Of Many Benzylic Bromides Using Molecular Bromine As A Halogenating Agent In The Presence Of Catalytic Amounts Of Lanthanum Triacetate Cheminform. 14. DOI: 10.1002/Chin.198311128 |
0.349 |
|
| 1982 |
Souppe J, Namy JL, Kagan HB. Samarium diiodide as coupling agent between aldehydes and organic halides for the synthesis of homoallylic and homobenzylic alcohols Tetrahedron Letters. 23: 3497-3500. DOI: 10.1016/S0040-4039(00)87651-0 |
0.346 |
|
| 1982 |
Levine-Pinto H, Morgat JL, Fromageot P, Meyer D, Poulin JC, Kagan HB. Asymmetric tritiation of N-acetyl dehydrophenylalanyl-(S) phenylalanine (methylester) catalyzed with a rhodium (+) diop complex Tetrahedron. 38: 119-123. DOI: 10.1016/0040-4020(82)85053-9 |
0.322 |
|
| 1982 |
Poulin JC, Kagan HB. A direct preparation of acetyl-(S)-phenylalanyl-(S)-phenylalanine methyl ester by a double asymmetric hydrogenation Journal of the Chemical Society, Chemical Communications. 1261-1262. DOI: 10.1002/Chin.198315336 |
0.303 |
|
| 1981 |
Girard P, Couffignal R, Kagan HB. An easy coupling of acid chlorides into α-diketones promoted by diiodosamarium Tetrahedron Letters. 22: 3959-3960. DOI: 10.1016/S0040-4039(01)82037-2 |
0.363 |
|
| 1981 |
Zhang SY, Yemul S, Kagan HB, Stern R, Commereuc D, Chauvin Y. Cyclodiop, an example of a new class of chiral diphosphines Tetrahedron Letters. 22: 3955-3958. DOI: 10.1016/S0040-4039(01)82036-0 |
0.396 |
|
| 1981 |
Kagan HB, Namy JL, Girard P. Divalent lanthanide derivatives in organic synthesis - II: Mechanism of SmI2 reactions in presence of ketones and organic halides Tetrahedron. 37: 175-180. DOI: 10.1016/0040-4020(81)85053-3 |
0.345 |
|
| 1981 |
Barry J, Kagan HB. Synthesis Of Enantiomers Of 1,2‐Heptanediol Cheminform. 12: 453-455. DOI: 10.1002/Chin.198143119 |
0.403 |
|
| 1981 |
Samuel O, Couffignal R, Lauer M, Zhang SY, Kagan HB. Phellanphos And Nopaphos, New Diphosphines For Asymmetric Catalysis Cheminform. 12. DOI: 10.1002/Chin.198122258 |
0.331 |
|
| 1981 |
Poulin J-, Meyer D, Kagan HB. Asymmetric Synthesis Of Dipeptides By Reduction Of A Bisdehydrodipeptide Cheminform. 12. DOI: 10.1002/Chin.198104097 |
0.426 |
|
| 1980 |
Kagan HB. Chiral Ligands In Asymmetric Catalysis By Transition Metal Complexes Annals of the New York Academy of Sciences. 333: 1-15. DOI: 10.1111/J.1749-6632.1980.Tb53624.X |
0.323 |
|
| 1980 |
Meyer D, Poulin JC, Kagan HB, Levine-Pinto H, Morgat JL, Fromageot P. Stereoselective synthesis of dipeptides by asymmetric reduction of dehydropeptides catalyzed by chiral rhodium complexes Journal of Organic Chemistry. 45: 4680-4682. DOI: 10.1021/Jo01311A026 |
0.48 |
|
| 1980 |
Girard P, Namy JL, Kagan HB. Divalent lanthanide derivatives in organic synthesis. 1. Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agents Journal of the American Chemical Society. 102: 2693-2698. DOI: 10.1021/Ja00528A029 |
0.344 |
|
| 1980 |
Yemul SS, Kagan HB, Setton R. Selective fluorination by C19XeF6 Tetrahedron Letters. 21: 277-280. DOI: 10.1016/S0040-4039(00)71188-9 |
0.327 |
|
| 1980 |
Peyronel J-, Fiaud J-, Kagan HB. Asymmetric Hydrosilylation Of Ketones Catalyzed By Chiral Rhodium Complexes Cheminform. 11. DOI: 10.1002/Chin.198051235 |
0.458 |
|
| 1980 |
Kagan HB, Fiaud JC, Hoornaert C, Meyer D, Poulin JC. Synthesis Of New Chiral Phosphines For Asymmetric Catalysis Cheminform. 11. DOI: 10.1002/Chin.198018261 |
0.452 |
|
| 1980 |
Cesarotti E, Ugo R, Kagan HB. Complexes With Chiral Alkylcyclopentadienyl Ligands For The Homogeneous Catalysis Of The Asymmetric Hydrogenation Of 2‐Phenyl‐1‐Butene Cheminform. 11. DOI: 10.1002/Chin.198004096 |
0.37 |
|
| 1979 |
Lauer M, Samuel O, Kagan HB. Synthesis of phellanphos, an efficient chiral 1,2-diphosphine for asymmetric catalysis Journal of Organometallic Chemistry. 177: 309-312. DOI: 10.1016/S0022-328X(00)92357-X |
0.458 |
|
| 1979 |
Kagan HB, Mimoun H, Mark C, Schurig V. Asymmetric Epoxidation Of Simple Olefins With An Optically Active Molybdenum(Vi) Peroxo Complex Cheminform. 10. DOI: 10.1002/Chin.197939149 |
0.309 |
|
| 1979 |
KAGAN HB, YAMAGISHI T, MOTTE JC, SETTON R. ChemInform Abstract: A GRAPHITE SUPPORTED CHIRAL CATALYST Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197936312 |
0.379 |
|
| 1979 |
Cesarotti E, Ugo R, Kagan HB. Complexes with Chiral Alkylcyclopentadienyl Ligands for Homogeneous Catalytic Asymmetric Hydrogenation of 2‐Phenyl‐1‐butene Angewandte Chemie. 18: 779-780. DOI: 10.1002/Anie.197907791 |
0.383 |
|
| 1979 |
Kagan HB, Mimoun H, Mark C, Schurig V. Asymmetric Epoxidation of Simple Olefins with an Optically Active Molybdenum(VI) Peroxo Complex Angewandte Chemie International Edition in English. 18: 485-486. DOI: 10.1002/Anie.197904851 |
0.309 |
|
| 1978 |
Detellier C, Gelbard G, Kagan HB. Asymmetric catalysis with chiral complexes of rhodium-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)-butane. 6. On the mechanism of reduction of (E,Z)-α-acylaminocinnamic acids with homogeneous rhodium catalysts Journal of the American Chemical Society. 100: 7556-7561. DOI: 10.1021/Ja00492A020 |
0.415 |
|
| 1978 |
Fiaud JC, de Gournay AH, Larcheveque M, Kagan HB. Asymmetric catalytic allylation of β-diketones or β-ketoesters with allylic ethers using a palladium-DIOP catalyst: A mechanistic study Journal of Organometallic Chemistry. 154: 175-185. DOI: 10.1016/S0022-328X(00)83439-7 |
0.387 |
|
| 1978 |
Cesarotti E, Kagan HB, Goddard R, Krüger C. Synthesis of new ligands for transition metal complexes: menthyl- and neomenthyl-cyclopentadienes Journal of Organometallic Chemistry. 162: 297-309. DOI: 10.1016/S0022-328X(00)81401-1 |
0.346 |
|
| 1978 |
Kagan HB, Yamagishi T, Motte JC, Setton R. A Graphite Supported Chiral Catalyst Israel Journal of Chemistry. 17: 274-277. DOI: 10.1002/Ijch.197800049 |
0.414 |
|
| 1977 |
Namy JL, Girard P, Kagan HB. A New Preparation Of Some Divalent Lanthanide Iodides And Their Usefulness In Organic Synthesis Cheminform. 8. DOI: 10.1002/Chin.197724312 |
0.342 |
|
| 1976 |
Sinou D, Kagan HB. Catalyse asymetrique par le complexe cationique [Rh(COD)(+)Diop]+ClO4 - Journal of Organometallic Chemistry. 114: 325-337. DOI: 10.1016/S0022-328X(00)87290-3 |
0.385 |
|
| 1976 |
Brunie S, Mazan J, Langlois N, Kagan HB. Catalyse asymetrique et structure du complexe IrCOD((+)-diop)Cl Journal of Organometallic Chemistry. 114: 225-232. DOI: 10.1016/S0022-328X(00)87239-3 |
0.301 |
|
| 1976 |
Gelbard G, Kagan HB, Stern R. Catalyse asymetrique avec des complexes chiraux de rhodium-diop-V. Effets des substituants lors de la reduction d'acides N-acylamino cinnamiques Tetrahedron. 32: 233-237. DOI: 10.1016/0040-4020(76)87007-X |
0.396 |
|
| 1976 |
Nicoud JF, Kagan HB. A New Case of Asymmetric Synthesis Using Circularly Polarized Light Israel Journal of Chemistry. 15: 78-81. DOI: 10.1002/Ijch.197600015 |
0.352 |
|
| 1976 |
Brunie S, Mazan J, Langlois N, Kagan HB. Asymmetric Catalysis And Structure Of The Complex, Chlorocyclooctadiene((+)-Isopropylidene-2,3-Dihydroxy-1,4-Bis(Diphenylphosphino)Butane)Iridium Cheminform. 7. DOI: 10.1002/Chin.197641341 |
0.335 |
|
| 1976 |
Gelbard G, Kagan HB, Stern R. Asymmetric Catalysis With Chiral Rhodium-Diop Complexes. V. Substituent Effects On The Reduction Of N-Acylaminocinnamic Acids Cheminform. 7. DOI: 10.1002/Chin.197614082 |
0.383 |
|
| 1975 |
dang TP, Poulin Jc, Kagan HB. Reduction asymetrique catalysee par des complexes de metaux de transition. III. Diphosphines chirales derivees de l'isopropylidene dihydroxy-2,3 bis(diphenylphosphino)-1,4 butane (diop) Journal of Organometallic Chemistry. 91: 105-115. DOI: 10.1016/S0022-328X(00)91878-3 |
0.433 |
|
| 1975 |
Poulin JC, Dang TP, Kagan HB. Hydrogenation catalytique homogene a l'aide de complexes rhodium-diphosphines Journal of Organometallic Chemistry. 84: 87-92. DOI: 10.1016/S0022-328X(00)88777-X |
0.362 |
|
| 1975 |
Kagan HB, Langlois N, Phat Dang T. Reduction asymetrique catalysee par des complexes de metaux de transition IV. synthese d'amines chirales au moyen d'un complexe de rhodium et d'isopropylidene dihydroxy-2,3 bis(diphenylphosphino)-1,4 butane (diop) Journal of Organometallic Chemistry. 90: 353-365. DOI: 10.1016/S0022-328X(00)88129-2 |
0.43 |
|
| 1975 |
Kagan HB. Asymmetric catalysis by chiral rhodium complexes in hydrogenation and hydrosilylation reactions Pure and Applied Chemistry. 43: 401-421. DOI: 10.1002/Chin.197622064 |
0.426 |
|
| 1975 |
Dang TP, Poulin JC, Kagan HB. Asymmetrische, Durch Uebergangsmetallkomplexe Katalysierte Reduktion 3. Mitt. Chirale Von Isopropyliden-Dihydroxy-2,3-Bis-(Diphenylphosphine)-1,4-Butan (Diop) Abgeleitete Diphosphine Cheminform. 6. DOI: 10.1002/Chin.197535291 |
0.434 |
|
| 1974 |
Balavoine G, Moradpour A, Kagan HB. Preparation of chiral compounds with high optical purity by irradiation with circularly polarized light, a model reaction for the prebiotic generation of optical activity Journal of the American Chemical Society. 96: 5152-5158. DOI: 10.1021/Ja00823A023 |
0.323 |
|
| 1973 |
Dumont W, Foulin JC, Dang TP, Kagan HB. Asymmetric catalytic reduction with transition metal complexes. II. Asymmetric catalysis by a supported chiral rhodium complex Journal of the American Chemical Society. 95: 8295-8299. DOI: 10.1021/Ja00806A015 |
0.354 |
|
| 1973 |
Langlois N, Dang TP, Kagan HB. Synthese asymetrique d'amines par hydrosilylation d'imines catalysee par un complexe chiral du rhodium Tetrahedron Letters. 14: 4865-4868. DOI: 10.1016/S0040-4039(01)87358-5 |
0.323 |
|
| 1972 |
Kagan HB, Dang TP. Asymmetric catalytic reduction with transition metal complexes. I. A catalytic system of rhodium(I) with (-)-2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino) butane, a new chiral diphosphine Journal of the American Chemical Society. 94: 6429-6433. DOI: 10.1021/Ja00773A028 |
0.374 |
|
| 1972 |
Decazes JM, Luche JL, Kagan HB, Parthasarathy R, Ohrt J. Cycloaddition Von Ketenen Mit Schiffschen Basen 5. Mitt. Struktur Und Stereochemie Der In Fluessigem Schwefeldioxid Gebildeten Addukte Cheminform. 3. DOI: 10.1002/Chin.197250258 |
0.304 |
|
| 1971 |
Dang TP, Kagan HB. The asymmetric synthesis of hydratropic acid and amino-acids by homogeneous catalytic hydrogenation Journal of the Chemical Society D: Chemical Communications. 481. DOI: 10.1039/C29710000481 |
0.363 |
|
| 1971 |
Fiaud J‐, Kagan HB. Asymmetrische Synth. Von Aminosaeuren, Untersuchungen Ueber Die Addition Metallorganischer Verbindungen An Imine Von Glyoxylsaeureestern Cheminform. 2. DOI: 10.1002/Chin.197130368 |
0.333 |
|
| 1970 |
Fiaud JC, Kagan HB. [New synthesis of alpha-amino acids. Asymmetric synthesis of alanine]. Tetrahedron Letters. 1813-6. PMID 5433532 DOI: 10.1016/S0040-4039(01)98090-6 |
0.337 |
|
| 1970 |
Decazes J, Luche JL, Kagan HB. Cycloaddition Von Keten An Schiffsche Basen 3. Mitt. Nmr-Spektroskopische Bestimmung Der Konformation Von 1,3,4-Triphenyl-3-Alkyl-2-Azetidinonen 4. Mitt. Stereochemie Der Addition Von Keto-Keten An Benzalanilin Cheminform. 1. DOI: 10.1002/Chin.197048324 |
0.373 |
|
| 1957 |
KAGAN HB, JACQUES J. [3 alpha-Hydroxy-delta 6-cholenic acid & 3 alpha, 6 beta, 7 beta-trihydroxycholanic acid]. Comptes Rendus Hebdomadaires Des SéAnces De L'AcadéMie Des Sciences. 245: 2417-20. PMID 13511740 |
0.409 |
|
| Show low-probability matches. |
