Rational Design of Highly Diastereoselective, Organic Base-Catalyzed, Room-Temperature Michael Addition Reactions1-Reference-Cited by-同舟云学术

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Rational Design of Highly Diastereoselective, Organic Base-Catalyzed, Room-Temperature Michael Addition Reactions1

Published:2000-09-13 Issue:20 Volume:65 Page:6688-6696
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Soloshonok Vadim A.¹,Cai Chaozhong¹,Hruby Victor J.¹,Meervelt Luc Van²,Yamazaki Takashi³

Affiliation:

1. Department of Chemistry, University of Arizona, Tucson, Arizona 85721

2. K. U. Leuven - Department of Chemistry, Celestijnenlaan 200F, B-3001 Heverlee-Leuven, Belgium

3. Department of Bioengineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0008791

Reference41 articles.

1. Stereochemically defined C-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3-trifluoromethylpyroglutamic acids

2. (a) Oare, D. A.; Heathcock, C. H. InTopics in Stereochemistry; Eliel, E. L., Wilen, S. H., Eds.; Wiley: New York, 1990; Vol. 19, pp 227−407.

3. Acyclic stereoselection. 46. Stereochemistry of the Michael addition of N,N-disubstituted amide and thioamide enolates to .alpha.,.beta.-unsaturated ketones

4. Highly diastereoselective Michael addition of lithiated camphor imines of glycine esters to .alpha.,.beta.-unsaturated esters. Synthesis of optically pure 5-oxo-2,4-pyrrolidinedicarboxylates of unnatural stereochemistry

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