A Surprising Mechanistic “Switch” in Lewis Acid Activation: A Bifunctional, Asymmetric Approach to α-Hydroxy Acid Derivatives-Reference-Cited by-同舟云学术

A Surprising Mechanistic “Switch” in Lewis Acid Activation: A Bifunctional, Asymmetric Approach to α-Hydroxy Acid Derivatives

Published:2008-11-17 Issue:50 Volume:130 Page:17085-17094
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Abraham Ciby J.¹,Paull Daniel H.¹,Bekele Tefsit¹,Scerba Michael T.¹,Dudding Travis¹,Lectka Thomas¹

Affiliation:

1. Department of Chemistry, New Chemistry Building, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218, and Department of Chemistry, Brock University, St. Catharines, Ontario L2S 3A1, Canada

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja806818a

Reference62 articles.

1. “Orthogonal” Lewis Acids: Catalyzed Ring Opening and Rearrangement of Acylaziridines

2. Catalytic, Enantioselective Bifunctional Inverse Electron Demand Hetero-Diels−Alder Reactions of Ketene Enolates and o-Benzoquinone Diimides

3. An Asymmetric, Bifunctional Catalytic Approach to Non-Natural α-Amino Acid Derivatives

4. Catalytic, Asymmetric Inverse Electron Demand Hetero Diels-Alder Reactions of o-Benzoquinone Derivatives and Ketene Enolates

5. Bifunctional Asymmetric Catalysis: Cooperative Lewis Acid/Base Systems

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