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

dc.contributor.authorBailey, Simon
dc.contributor.authorDavies, Stephen G.
dc.contributor.authorSmith, Andrew D.
dc.contributor.authorWithey, Jonathan
dc.date.accessioned2015-04-17
dc.date.accessioned2022-05-27T01:13:47Z
dc.date.available2022-05-27T01:13:47Z
dc.date.issued2002
dc.description.abstractThe 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.
dc.description.urihttp://library.macewan.ca/cgi-bin/SFX/url.pl/7LY
dc.format.extent34 kb
dc.identifierhttps://doi.org/10.1039/b209728c
dc.identifier.citationBailey, 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
dc.identifier.urihttps://hdl.handle.net/20.500.14078/278
dc.languageEnglish
dc.language.isoen
dc.rightsAll Rights Reserved
dc.subjectasymmetric synthesis
dc.subjectkinetic resolution protocol
dc.titleAsymmetric synthesis of (1R,2S,3R)-gamma-methyl-cis-pentacin by a kinetic resolution protocol
dc.titleAsymmetric synthesis of (1R,2S,3R)-gamma-methyl-cis-pentacin by a kinetic resolution protocol
dc.typeArticle
dspace.entity.type
Files