Asymmetric Formation of α-Amino Acid Esters through Dynamic Kinetic Resolution: A Cyclic Carbonate as an Optically Active CO2 Synthon
- 27 April 1999
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (18), 4520-4521
- https://doi.org/10.1021/ja984061x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Dynamic resolutions in asymmetric synthesisChemical Society Reviews, 1996
- Origin of Stereochemistry in the α-Amino Acid Esters and Amides Generated from Optically Active Zirconaaziridine Complexes1Journal of the American Chemical Society, 1996
- Dynamic kinetic resolutionTetrahedron: Asymmetry, 1995
- Stereoselective Organic Synthesis via Dynamic Kinetic ResolutionBulletin of the Chemical Society of Japan, 1995
- Insertion of Isocyanates, CO2, and Ethylene Carbonate into the Zr-C and Zr-N Bonds of Imine Complexes. Construction of Chiral Centers Like Those in .alpha.-Amino AcidsJournal of the American Chemical Society, 1995
- Structure-reactivity correlations for the formation of zirconocene .eta.2-imine complexes from aminesOrganometallics, 1994
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Zirconocene complexes of imines. General synthesis, structure, reactivity, and in situ generation to prepare geometrically pure allylic aminesJournal of the American Chemical Society, 1989
- Effect of conformational change on reactivity in organic chemistry. Evaluations, applications, and extensions of Curtin-Hammett Winstein-Holness kineticsChemical Reviews, 1983
- Studies on the Racemization of Amino Acids and their Derivatives. I. On the Deuterium-Hydrogen Exchange Reaction of Amino Acids Derivatives in Basic MediaCHEMICAL & PHARMACEUTICAL BULLETIN, 1967