Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction
- 1 July 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (27) , 3151-3154
- https://doi.org/10.1016/s0040-4039(00)79708-5
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Efficient and practical asymmetric synthesis of the taxol C-13 side chain, N-benzoyl-(2R,3S)-3-phenylisoserine, and its analogs via chiral 3-hydroxy-4-aryl-.beta.-lactams through chiral ester enolate-imine cyclocondensationThe Journal of Organic Chemistry, 1991
- A novel synthesis of the (2R,3S)- and (2S3R)-3-amino-2-hydroxycarboxylic acid derivatives, the key components of a renin inhibitor and bestatin, from methyl (R)- and (S-mandelateTetrahedron Letters, 1990
- Taxol: A Novel Investigational Antimicrotubule AgentJNCI Journal of the National Cancer Institute, 1990
- An improved synthesis of the taxol side chain and of RP 56976The Journal of Organic Chemistry, 1990
- Chemo-enzymatic synthesis of all isomeric 3-phenylserines and -isoserinesTetrahedron, 1990
- Addition of α-bromoesters to azetidine-2,3-diones promoted by zinc-trimethylchlorosilane: a general synthesis of 3-trimethyisilyloxyazetidin-2-ones and α-alkylidene β-lactams.Tetrahedron Letters, 1990
- The Chemistry of Taxol, a Clinically Useful Anticancer AgentJournal of Natural Products, 1990
- Highly efficient, practical approach to natural taxolJournal of the American Chemical Society, 1988
- Chiral control of the Staudinger reactionPublished by Walter de Gruyter GmbH ,1987
- An efficient, enantioselective synthesis of the taxol side chainThe Journal of Organic Chemistry, 1986