Palladium-Catalyzed Asymmetric Allylic Alkylation of 2-Acylimidazoles as Ester Enolate Equivalents-Reference-Cited by-同舟云学术

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Palladium-Catalyzed Asymmetric Allylic Alkylation of 2-Acylimidazoles as Ester Enolate Equivalents

Published:2010-06-15 Issue:26 Volume:132 Page:8915-8917
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Trost Barry M.¹,Lehr Konrad¹,Michaelis David J.¹,Xu Jiayi¹,Buckl Andreas K.¹

Affiliation:

1. Department of Chemistry, Stanford University, Stanford, California 94305-5080

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja103771w

Reference33 articles.

1. For reviews, see:

2. aEvans, D. A.InAsymmetric Synthesis;Morrison, J. D., Ed.Academic Press:New York, 1983; Vol.3,Chapter 1, pp83−110.

3. bMeyers, A. I.InAsymmetric Synthesis;Morrison, J. D., Ed.Academic Press:New York, 1983; Vol.3,Chapter 3, pp213−274.

4. For recent reviews, see:

5. Advances in Asymmetric Enolate Methodology

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