Recent progress in Lewis acid-Lewis base bifunctional asymmetric catalysis-Reference-Cited by-同舟云学术

Recent progress in Lewis acid-Lewis base bifunctional asymmetric catalysis

Published:2005-01-01 Issue:12 Volume:77 Page:2047-2052
ISSN:1365-3075
Container-title:Pure and Applied Chemistry
language:
Short-container-title:

Author:

Kanai Motomu¹,Kato Nobuki²,Ichikawa Eiko²,Shibasaki Masakatsu¹

Affiliation:

1. 1Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan

2. 2PRESTO, Japan Science and Technology Corporation (JST), 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Abstract

Two enantioselective cyanation reactions, the Strecker reaction of ketoimines and the Reissert reaction of pyridine derivatives, promoted by Lewis acid-Lewis base bifunctional asymmetric catalysts are described.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Link

https://www.degruyter.com/document/doi/10.1351/pac200577122047/pdf

Reference6 articles.

1. For the original communication see a;Kato;Tetrahedron Lett Tetrahedron Lett,2004

2. a and and;Vachal;Lett Am Chem Soc,2000

3. For reviews see a and and;Cativiela;Tetrahedron Asymmetry Bull Chem Soc Jpn,1998

4. a a and Bifunctional asymmetric catalysis Scheme Catalytic enantioselective Reissert reaction of pyridine derivatives a a;Shibasaki;Chem Commun Am Chem Soc Tetrahedron Angew Chem Ed Chem Pharm Bull Pure Applied Chemistry Am Chem Soc Am Chem Soc Am Chem Soc Am Chem Soc Tetrahedron Lett Am Chem Soc,2002

5. For the original communication see;Ichikawa;Am Chem Soc,2004

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