2-Aryl-4,4,8-trimethyl-2-phosphabicyclo[3.3.0]octanes: Reactive Chiral Phosphine Catalysts for Enantioselective Acylation
- 1 June 1999
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (24) , 5813-5814
- https://doi.org/10.1021/ja990133o
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Mathematical Description of Kinetic Resolution with an Enantiomerically Impure Catalyst and Nonracemic SubstrateThe Journal of Organic Chemistry, 1998
- Kinetic Resolution of Arylalkylcarbinols Catalyzed by a Planar-Chiral Derivative of DMAP: A New Benchmark for Nonenzymatic AcylationThe Journal of Organic Chemistry, 1998
- Nonenzymatic Kinetic Resolution of Racemic Alcohols through an “Induced Fit” ProcessJournal of the American Chemical Society, 1997
- Nonenzymatic enantioselective acylation of racemic secondary alcohols catalyzed by a SnX2-chiral diamine complexTetrahedron Letters, 1996
- Enantioselective Acylations Catalyzed by Chiral PhosphinesThe Journal of Organic Chemistry, 1996
- Preparation and use of C2-symmetric bis(phospholanes): production of .alpha.-amino acid derivatives via highly enantioselective hydrogenation reactionsJournal of the American Chemical Society, 1993
- Resolution of Enantiomers via BiocatalysisTopics in Stereochemistry, 1989
- Kinetic ResolutionPublished by Wiley ,1988