Kinetic Resolution of Racemic α-tert-Alkyl-α-hydroxy Esters by Enantiomer-Selective Carbamoylation

Author:

Kurono Nobuhito1,Ohtsuga Kentaro1,Wakabayashi Masanori1,Kondo Tadahiro1,Ooka Hirohito1,Ohkuma Takeshi1

Affiliation:

1. Division of Chemical Process Engineering, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference44 articles.

1. α‐Hydroxy Acids in Enantioselective Syntheses

2. The chiral pool as a source of enantioselective catalysts and auxiliaries

3. The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks

4. Grabowski, E. J. J.InChiral Reagents for Asymmetric Synthesis;Paquette, L. A., Ed.Wiley:Chichester, 2003; pp335–338.

5. Tao, J.; McGee, K.InAsymmetric Catalysis on Industrial Scale: Challenges, Approaches, and Solutions;Blaser, H. U.; Schmidt, E., Eds.Wiley-VCH:Weinheim, Germany, 2004; pp323–334.

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