Asymmetric synthesis of (1R,2S,3R)-gamma-methyl-cis-pentacin by a kinetic resolution protocol Asymmetric synthesis of (1R,2S,3R)-gamma-methyl-cis-pentacin by a kinetic resolution protocol

Author
Bailey, Simon
Davies, Stephen G.
Smith, Andrew D.
Withey, Jonathan
Faculty Advisor
Date
2002
Keywords
asymmetric synthesis , kinetic resolution protocol
Abstract (summary)
The asymmetric synthesis of (1R,2S,3R)-3-methyl-2-amino-cyclopentane carboxylic acid has been achieved via kinetic resolution of racemic tert-butyl 3-methyl-cyclopentene-1-carboxylate with homochiral lithium (S)-N-benzyl-N-alpha-methylbenzylamide.
Publication Information
Bailey, S., Davies, S. G., Smith, A. D., & Withey, J. M. (2002). Asymmetric synthesis of (1R,2S,3R)-gamma-methyl-cis-pentacin by a kinetic resolution protocol. Chemical Communications, (23), 2910-2911. DOI: 10.1039/b209728c
Notes
Item Type
Article
Language
English
Rights
All Rights Reserved