Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary-Reference-Cited by-同舟云学术

Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary

Published:2006-07 Issue:7 Volume:79 Page:1069-1083
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ding Xia,Taniguchi Katsumi,Hamamoto Yoshihira,Sada Kazunori,Fujinami Shuhei,Ukaji Yutaka,Inomata Katsuhiko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference53 articles.

1. Asymmetric 1,3-Dipolar Cycloaddition Reactions

2. Catalytic enantioselective 1,3-dipolar cycloaddition reactions of nitrones

3. New Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar Cycloaddition

4. Chiral bis(trialkylsiloxymethyloxazolinyl)pyridine ligands. Highly enantioselective 1,3-dipolar cycloaddition reactions

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