Asymmetric Mukaiyama Aldol Reactions Using Chiral Diamine-Coordinated Sn(II) Triflate: Development and Application to Natural Product Synthesis-Reference-Cited by-同舟云学术

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Asymmetric Mukaiyama Aldol Reactions Using Chiral Diamine-Coordinated Sn(II) Triflate: Development and Application to Natural Product Synthesis

Published:2014-01-25 Issue:1 Volume:14 Page:144-183
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:The Chemical Record

Author:

Shiina Isamu¹

Affiliation:

1. Department of Applied Chemistry; Faculty of Science; Tokyo University of Science; 1-3 Kagurazaka Shinjuku-ku Tokyo 162-8601 Japan

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/tcr.201300022/fullpdf

Reference119 articles.

1. NEW ALDOL TYPE REACTION

2. New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

3. A NEW METHOD FOR THE PREPARATION OF β-HYDROXYESTERS. THE TITANIUM TETRACHLORIDE-PROMOTED REACTION OF KETENE ALKYL TRIALKYLSILYL ACETALS WITH CARBONYL COMPOUNDS

4. 3-HYDROXY-3-METHYL-1-PHENYL-1-BUTANONE BY CROSSED ALDOL REACTION

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