Synthesis of enantiomerically enriched Baylis–Hillman alcohols from their acetates: combination of kinetic resolution during the salt formation with (DHQD)2PHAL and following asymmetric induction during hydrolysis with NaHCO3 as a water surrogate-Reference-Cited by-同舟云学术

Synthesis of enantiomerically enriched Baylis–Hillman alcohols from their acetates: combination of kinetic resolution during the salt formation with (DHQD)2PHAL and following asymmetric induction during hydrolysis with NaHCO3 as a water surrogate

Published:2002-12 Issue:50 Volume:43 Page:9141-9146
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kim Jae Nyoung,Lee Hong Jung,Gong Ji Hyeon

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 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. New Strategies for the Development of an Asymmetric Version of the Baylis–Hillman Reaction

4. Synthesis of Cyclic Compounds from the Baylis-Hillman Adducts

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