Conjugate addition of Grignard reagents to enones and dienones-Reference-Cited by-同舟云学术

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Conjugate addition of Grignard reagents to enones and dienones

Published:1989-05 Issue:10 Volume:54 Page:2317-2321
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Modi Sandeep P.,Gardner John O.,Milowsky Arnold,Wierzba Mark,Forgione Lisa,Mazur Paul,Solo Alan J.,Duax William L.,Galdecki Z.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00271a014

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2. 7α-alkylation, 7,7-bisalkylation, and reduction of the 20-oxo group of poststerone in reactions with alkyl halides in lithium–ammonia solution;Russian Journal of Organic Chemistry;2017-01

3. Regio- and Stereoselective Preparation of β,γ-Unsaturated Carboxylic Acids by One-Pot Sequential Double 1,6-Addition of Grignard Reagents to Methyl Coumalate;Advanced Synthesis & Catalysis;2016-09-12

4. 7α-Alkylation and 7,7-bis-alkylation of 20-hydroxyecdysone with propargyl bromide in a lithium–ammonia solution and catalytic reductive spirocyclization of 7,7-bis(2-propyn-1-yl)-14-deoxy-Δ8(14)-20-hydroxyecdysone;Steroids;2016-03

5. C- and O-alkylation of ecdysteroids in lithium-ammonia solution;Russian Journal of Organic Chemistry;2015-11

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