Year |
Citation |
Score |
2013 |
Liljenberg M, Brinck T, Rein T, Svensson M. Utilizing the σ-complex stability for quantifying reactivity in nucleophilic substitution of aromatic fluorides. Beilstein Journal of Organic Chemistry. 9: 791-9. PMID 23766792 DOI: 10.3762/Bjoc.9.90 |
0.454 |
|
2013 |
Karlström S, Nordvall G, Sohn D, Hettman A, Turek D, Åhlin K, Kers A, Claesson M, Slivo C, Lo-Alfredsson Y, Petersson C, Bessidskaia G, Svensson PH, Rein T, Jerning E, et al. Substituted 7-amino-5-thio-thiazolo[4,5-d]pyrimidines as potent and selective antagonists of the fractalkine receptor (CX3CR1). Journal of Medicinal Chemistry. 56: 3177-90. PMID 23516963 DOI: 10.1021/Jm3012273 |
0.303 |
|
2012 |
Liljenberg M, Brinck T, Herschend B, Rein T, Tomasi S, Svensson M. Predicting regioselectivity in nucleophilic aromatic substitution Journal of Organic Chemistry. 77: 3262-3269. PMID 22384935 DOI: 10.1021/Jo202569N |
0.413 |
|
2012 |
Nilsson Lill SO, Ryberg P, Rein T, Bennström E, Norrby PO. tBu or not tBu? Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1640-9. PMID 22223125 DOI: 10.1002/Chem.201102674 |
0.649 |
|
2011 |
Liljenberg M, Brinck T, Herschend B, Rein T, Rockwell G, Svensson M. A pragmatic procedure for predicting regioselectivity in nucleophilic substitution of aromatic fluorides Tetrahedron Letters. 52: 3150-3153. DOI: 10.1016/J.Tetlet.2011.04.032 |
0.438 |
|
2010 |
Liljenberg M, Brinck T, Herschend B, Rein T, Rockwell G, Svensson M. Validation of a computational model for predicting the site for electrophilic substitution in aromatic systems Journal of Organic Chemistry. 75: 4696-4705. PMID 20552984 DOI: 10.1021/Jo100310V |
0.388 |
|
2010 |
Strand D, Rein T. [(BINAP)Re(O)Cl3] as an efficient catalyst for olefination of chiral α-substituted aliphatic aldehydes Journal of Organometallic Chemistry. 695: 2220-2224. DOI: 10.1016/J.Jorganchem.2010.06.008 |
0.615 |
|
2006 |
Strand D, Norrby PO, Rein T. Divergence en route to nonclassical annonaceous acetogenins. Synthesis of pyranicin and pyragonicin. The Journal of Organic Chemistry. 71: 1879-91. PMID 16496972 DOI: 10.1021/Jo052233K |
0.791 |
|
2006 |
Strand D, Norrby P-, Rein T. Synthesis of Pyranicin Synfacts. 2006: 754-754. DOI: 10.1055/S-2006-941926 |
0.733 |
|
2005 |
Strand D, Rein T. Synthesis of pyragonicin. Organic Letters. 7: 2779-81. PMID 15957945 DOI: 10.1055/S-2005-921663 |
0.636 |
|
2005 |
Strand D, Rein T. Total synthesis of pyranicin. Organic Letters. 7: 199-202. PMID 15646957 DOI: 10.1021/Ol0479242 |
0.706 |
|
2003 |
Pedersen B, Rein T, Søtofte I, Norrby PO, Tanner D. Diastereoselective addition of α-metalated sulfoxides to imines revisited: Mechanism, computational studies, and the effect of external chiral ligands Collection of Czechoslovak Chemical Communications. 68: 885-898. DOI: 10.1135/Cccc20030885 |
0.727 |
|
2003 |
Heumann A, Åkermark B, Hansson S, Rein T. Allylic Acetoxylation of Cycloalkenes: 2‐Cyclohepten‐1‐yl Acetate Organic Syntheses. 109-109. DOI: 10.1002/0471264180.Os068.14 |
0.665 |
|
2002 |
Vares L, Rein T. A versatile stereocontrolled approach to chiral tetrahydrofuran and tetrahydropyran derivatives by use of sequential asymmetric Horner-Wadsworth-Emmons and ring-closure reactions. The Journal of Organic Chemistry. 67: 7226-37. PMID 12375948 DOI: 10.1021/Jo0259111 |
0.58 |
|
2002 |
Humphrey JM, Liao Y, Ali A, Rein T, Wong YL, Chen HJ, Courtney AK, Martin SF. Enantioselective total syntheses of manzamine a and related alkaloids. Journal of the American Chemical Society. 124: 8584-92. PMID 12121099 DOI: 10.1021/Ja0202964 |
0.496 |
|
2002 |
Rein T, Pedersen TM. Asymmetric wittig type reactions Synthesis. 579-594. DOI: 10.1055/S-2002-23535 |
0.512 |
|
2001 |
Pedersen TM, Hansen EL, Kane J, Rein T, Helquist P, Norrby PO, Tanner D. Enantioconvergent synthesis by sequential asymmetric Horner-Wadsworth-Emmons and palladium-catalyzed allylic substitution reactions. Journal of the American Chemical Society. 123: 9738-42. PMID 11583534 DOI: 10.1021/Ja005809Q |
0.774 |
|
2001 |
Has-Becker S, Bodmann K, Kreuder R, Santoni G, Rein T, Reiser O. High-pressure induced domino-Horner-Wadsworth-Emmons (HWE) -Michael reactions Synlett. 1395-1398. DOI: 10.1055/S-2001-16786 |
0.479 |
|
2000 |
Vares L, Rein T. A versatile stereocontrolled approach to chiral tetrahydrofuran and tetrahydropyran derivatives via sequential asymmetric Horner-Wadsworth-Emmons and palladium-catalyzed ring closure reactions Organic Letters. 2: 2611-4. PMID 10990409 DOI: 10.1021/Ol006135R |
0.544 |
|
2000 |
Pedersen TM, Jensen JF, Humble RE, Rein T, Tanner D, Bodmann K, Reiser O. Parallel kinetic resolution of racemic aldehydes by use of asymmetric Horner-Wadsworth-Emmons reactions Organic Letters. 2: 535-8. PMID 10814370 DOI: 10.1021/Ol991387H |
0.568 |
|
1999 |
Rein T, Vares L, Kawasaki I, Pedersen TM, Norrby PO, Brandt P, Tanner D. Asymmetric Horner-Wadsworth-Emmons reactions with Meso-dialdehydes: Scope, mechanism, and synthetic applications Phosphorus, Sulfur and Silicon and Related Elements. 144: 169-172. DOI: 10.1080/10426509908546209 |
0.762 |
|
1999 |
Tullis JS, Helquist P, Rein T. Synthetic applications of asymmetric Horner-Wadsworth-Emmons condensations: Approaches to marine natural products Phosphorus, Sulfur and Silicon and Related Elements. 144: 165-168. DOI: 10.1080/10426509908546208 |
0.468 |
|
1999 |
Norrby PO, Brandt P, Rein T. Rationalization of product selectivities in asymmetric Horner-Wadsworth- Emmons reactions by use of a new method for transition-state modeling Journal of Organic Chemistry. 64: 5845-5852. DOI: 10.1021/Jo990318D |
0.719 |
|
1998 |
Tullis JS, Vares L, Kann N, Norrby PO, Rein T. Reagent control of geometric selectivity and enantiotopic group preference in asymmetric Horner-Wadsworth-Emmons reactions with meso- dialdehydes Journal of Organic Chemistry. 63: 8284-8294. DOI: 10.1021/Jo981102Z |
0.782 |
|
1998 |
Brandt P, Norrby PO, Martin I, Rein T. A Quantum Chemical Exploration of the Horner-Wadsworth-Emmons Reaction Journal of Organic Chemistry. 63: 1280-1289. DOI: 10.1021/Jo971973T |
0.699 |
|
1997 |
Kreuder R, Rein T, Reiser O. Versatile stereocontrol in kinetic resolution of a Diphenylphosphinyl-protected α-amino aldehyde by reaction with chiral phosphonates Tetrahedron Letters. 38: 9035-9038. DOI: 10.1016/S0040-4039(97)10428-2 |
0.508 |
|
1997 |
Mendlik MT, Cottard M, Rein T, Helquist P. Stereocontrolled synthesis of the C(1)-C(11) subunit of the Iejimalides Tetrahedron Letters. 38: 6375-6378. DOI: 10.1016/S0040-4039(97)01467-6 |
0.397 |
|
1996 |
Rein T, Reiser O. Recent advances in asymmetric Wittig-type reactions Acta Chemica Scandinavica. 50: 369-379. DOI: 10.3891/Acta.Chem.Scand.50-0369 |
0.455 |
|
1995 |
Cottard M, Kann N, Rein T, Åkermark B, Helquist P. Synthesis of a major subunit of the iejimalides Tetrahedron Letters. 36: 3115-3118. DOI: 10.1016/0040-4039(95)00486-V |
0.798 |
|
1995 |
Rein T, Anvelt J, Soone A, Kreuder R, Wulff C, Reiser O. Kinetic resolution of racemic aldehydes by reaction with chiral 2-phosphonopropionates Tetrahedron Letters. 36: 2303-2306. DOI: 10.1016/0040-4039(95)00240-D |
0.551 |
|
1994 |
Helquist P, Bergdahl M, Hett R, Gangloff AR, Demillequand M, Cottard M, Mader MM, Friebe T, Iqbal J, Wu Y, Åkermark B, Rein T, Kann N. Synthesis of macrocyclic lactam/lactone derivatives having antimicrobial activity Pure and Applied Chemistry. 66: 2063-2066. DOI: 10.1351/Pac199466102063 |
0.781 |
|
1994 |
Martin SF, Liao Y, Wong Y, Rein T. A novel approach to the asymmetric synthesis of manzamine A. Construction of the tetracyclic ABCE ring system Tetrahedron Letters. 35: 691-694. DOI: 10.1016/S0040-4039(00)75792-3 |
0.429 |
|
1994 |
Rein T, Kann N, Kreuder R, Gangloff B, Reiser O. Kinetic Resolution of the Acrolein Dimer by Asymmetric Horner-Wadsworth-Emmons Reactions†‡ Angewandte Chemie. 33: 556-558. DOI: 10.1002/Anie.199405561 |
0.723 |
|
1994 |
Rein T, Kann N, Kreuder R, Gangloff B, Reiser O. Kinetic resolution of the acrolein dimer by asymmetric Horner - Wadsworth - Emmons reactions Angewandte Chemie (International Edition in English). 33: 556-558. |
0.771 |
|
1993 |
Kann N, Rein T. Asymmetrie Horner-Wadsworth-Emmons reactions using meso dialdehydes as substrates Journal of Organic Chemistry. 58: 3802-3804. DOI: 10.1021/Jo00067A010 |
0.8 |
|
1991 |
Martin SF, Rein T, Liao Y. Construction of the tricyclic ABC ring subunit of manzamine A via a novel intramolecular Diels-Alder reaction Tetrahedron Letters. 32: 6481-6484. DOI: 10.1016/0040-4039(91)80198-F |
0.397 |
|
1990 |
Kann N, Rein T, Åkermark B, Helquist P. New functionalized Horner-Wadsworth-Emmons reagents: Useful building blocks in the synthesis of polyunsaturated aldehydes. A short synthesis of (±)-(E,E)-coriolic acid Journal of Organic Chemistry. 55: 5312-5323. DOI: 10.1021/Jo00306A006 |
0.756 |
|
1990 |
Hansson S, Heumann A, Rein T, Åkermark B. Preparation of allylic acetates from simple alkenes by palladium(II)-catalyzed acetoxylation Journal of Organic Chemistry. 55: 975-984. DOI: 10.1021/Jo00290A031 |
0.715 |
|
1989 |
Åkermark B, Hansson S, Rein T, Vgberg J, Heumann A, Bäckvall JE. Palladium-catalyzed allylic acetoxylation: an exploratory study of the influence of added acids Journal of Organometallic Chemistry. 369: 433-444. DOI: 10.1016/0022-328X(89)85192-7 |
0.695 |
|
1988 |
Rein T, Akermark B, Helquist P. Synthesis of polyconjugated aldehydes using a new Horner--Wadsworth--Emmons reagent. Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry. 42: 569-72. PMID 3227743 |
0.668 |
|
1988 |
Connell RD, Rein T, Åkermark B, Helquist P. An efficient, palladium-catalyzed route to protected allylic amines Journal of Organic Chemistry. 53: 3845-3849. DOI: 10.1021/Jo00251A035 |
0.613 |
|
1985 |
AKERMARK B, NYSTROEM J, REIN T, BAECKVALL J, HELQUIST P, ASLANIAN R. ChemInform Abstract: Facile Route to 1-Phosphoryl- and l-Sulfonyl-1,3-dienes via Palladium-Catalyzed Elimination of Allylic Acetates. Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198519267 |
0.623 |
|
1984 |
Åkermark B, Nyström JE, Rein T, Bäckvall JE, Helquist P, Aslanian R. Facile route to 1-phosphoryl- and 1-sulfonyl-1,3-dienes via palladium-catalyzed elimination of allylic acetates Tetrahedron Letters. 25: 5719-5722. DOI: 10.1016/S0040-4039(01)81668-3 |
0.706 |
|
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