Novel Asymmetric C−C Bond Formation Process Promoted by Et2AlCl and Its Application to the Stereoselective Synthesis of Unusual β-Branched Baylis−Hillman Adducts-Reference-Cited by-同舟云学术

Novel Asymmetric C−C Bond Formation Process Promoted by Et2AlCl and Its Application to the Stereoselective Synthesis of Unusual β-Branched Baylis−Hillman Adducts

Published:1999-01-13 Issue:3 Volume:64 Page:1061-1064
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Guigen¹,Wei Han-Xun¹,Whittlesey Bruce R.¹,Batrice Nassim N.¹

Affiliation:

1. Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409-1061

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981976l

Reference42 articles.

1. The Baylis-Hillman reaction: A novel carbon-carbon bond forming reaction

2. Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydes

3. The Asymmetric Baylis−Hillman Reaction

4. Catalytic enantioselective Baylis-Hillman reactions. Correlation between pressure and enantiomeric excess

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