Asymmetric Carbon−Carbon Bond Formation in Michael Reactions: Conjugate Addition Reactions of Configurationally Stable Benzylic and Allylic Organolithium Species-Reference-Cited by-同舟云学术

Asymmetric Carbon−Carbon Bond Formation in Michael Reactions: Conjugate Addition Reactions of Configurationally Stable Benzylic and Allylic Organolithium Species

Published:1999-04-01 Issue:9 Volume:64 Page:2996-2997
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Curtis M. D.¹,Beak P.¹

Affiliation:

1. Department of Chemistry, University of Illinois at Urbana−Champaign, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990383n

Reference17 articles.

1. Acceleration of the conjugate addition of diethyl zinc to enones by either Cu(OTf)2 or trivalent phosphorus ligands

2. A Catalytic Asymmetric Synthesis of 11-Deoxy-PGF1α Using ALB, a Heterobimetallic Multifunctional Asymmetric Complex

3. Asymmetric conjugate addition

4. Conjugate Allylation toα,β-Unsaturated Aldehydes with the New Chemzymep-F-ATPH

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