Concerted Amidation of Activated Esters: Reaction Path and Origins of Selectivity in the Kinetic Resolution of Cyclic Amines via N-Heterocyclic Carbenes and Hydroxamic Acid Cocatalyzed Acyl Transfer-Reference-Cited by-同舟云学术

Concerted Amidation of Activated Esters: Reaction Path and Origins of Selectivity in the Kinetic Resolution of Cyclic Amines via N-Heterocyclic Carbenes and Hydroxamic Acid Cocatalyzed Acyl Transfer

Published:2014-08-08 Issue:33 Volume:136 Page:11783-11791
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Allen Scott E.¹,Hsieh Sheng-Ying²,Gutierrez Osvaldo¹,Bode Jeffrey W.²,Kozlowski Marisa C.¹

Affiliation:

1. Department of Chemistry, Roy and Diana Vagelos Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States

2. Laboratorium für Organische Chemie, ETH-Zürich, Zürich 8093, Switzerland

Funder

Division of Chemistry

European Research Council

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja505784w

Reference57 articles.

1. Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols

2. Evolution of asymmetric organocatalysis: multi- and retrocatalysis

3. Nonenzymatic Acylative Kinetic Resolution of Racemic Amines and Related Compounds

4. Theoretical Prediction of Selectivity in Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral DMAP Derivatives

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