Experimental Evidence for Chair-Like Transition States in Aldol Reactions of Methyl Ketone Lithium Enolates: Stereoselective Synthesis and Utilization of a Deuterium-Labeled Enolate as a Probe of Reaction Stereochemistry-Reference-Cited by-同舟云学术

Experimental Evidence for Chair-Like Transition States in Aldol Reactions of Methyl Ketone Lithium Enolates: Stereoselective Synthesis and Utilization of a Deuterium-Labeled Enolate as a Probe of Reaction Stereochemistry

Published:2005-04-01 Issue:16 Volume:127 Page:5770-5771
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Christopher M.¹,Smith William J.¹,Gustin Darin J.¹,Roush William R.¹

Affiliation:

1. Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja050730c

Reference17 articles.

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3. Diastereoselective Aldol and Allylstannane Addition Reactions. The Merged Stereochemical Impact of .alpha. and .beta. Aldehyde Substituents

4. Resurrecting the Cornforth Model for Carbonyl Addition: Studies on the Origin of 1,2-Asymmetric Induction in Enolate Additions to Heteroatom-Substituted Aldehydes

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