Highly Enantioselective Direct Alkylation of Arylacetic Acids with Chiral Lithium Amides as Traceless Auxiliaries-Reference-Cited by-同舟云学术

Highly Enantioselective Direct Alkylation of Arylacetic Acids with Chiral Lithium Amides as Traceless Auxiliaries

Published:2011-07-15 Issue:31 Volume:133 Page:11936-11939
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Stivala Craig E.¹,Zakarian Armen¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja205107x

Reference43 articles.

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2. Caine, D.InComprehensive Organic Synthesis;Trost, B. M. and Fleming, I., Eds.Pergamon Press:New York, 1991; Vol.3, pp1–63.

3. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives

4. New procedure for the direct generation of titanium enolates. Diastereoselective bond constructions with representative electrophiles

5. Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis

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