Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy-Reference-Cited by-同舟云学术

Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy

Published:2001-09 Issue:38 Volume:57 Page:8167-8172
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Basavaiah Deevi,Kumaragurubaran Nagaswamy,Sharada Duddu S,Reddy Ravi Mallikarjuna

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

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

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

3. DABCO-catalyzed coupling of aldehydes with activated double bonds. 4. Stereoselective synthesis of trisubstituted olefins and terpenoid building blocks via 2-(hydroxyalkyl)-2-propenoic esters

4. Deracemization of Baylis−Hillman Adducts

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