Applications of Baylis–Hillman coupling products: a remarkable reversal of stereochemistry from esters to nitriles: a simple synthesis of (2E)-2-methylalk-2-en-1-ols and (2Z)-2-methylalk-2-enenitriles-Reference-Cited by-同舟云学术

Applications of Baylis–Hillman coupling products: a remarkable reversal of stereochemistry from esters to nitriles: a simple synthesis of (2E)-2-methylalk-2-en-1-ols and (2Z)-2-methylalk-2-enenitriles

Published:1992 Issue:13 Volume:0 Page:955-957
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Basavaiah Deevi,Sarma Pakala K. S.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1992/C3/C39920000955

Reference20 articles.

1. Preparation of 2-(1-Hydroxyalkyl)acrylic Esters; Simple Three-Step Synthesis of Mikanecic Acid

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

3. Preparation and nucleophilic substitution of (e)-1-bromo-2-phenylsulfonyl-2-alkenes and 3-acetoxy-2-phenylsulfonyl-1-alkenes

4. A Novel Reaction of Ethyl 2,3-Butadienoate with Aldehydes in the Presence of Base

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