Catalytic Kinetic Resolution of Disubstituted Piperidines by Enantioselective Acylation: Synthetic Utility and Mechanistic Insights-Reference-Cited by-同舟云学术

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Catalytic Kinetic Resolution of Disubstituted Piperidines by Enantioselective Acylation: Synthetic Utility and Mechanistic Insights

Published:2015-08-26 Issue:35 Volume:137 Page:11491-11497
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wanner Benedikt¹,Kreituss Imants¹,Gutierrez Osvaldo²,Kozlowski Marisa C.²,Bode Jeffrey W.¹

Affiliation:

1. Laboratorium für Organische Chemie, Department of Chemistry and Applied Biosciences, ETH-Zürich, 8093 Zürich, Switzerland

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

Funder

European Research Council

National Institutes of Health

Division of Chemistry

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b07201

Reference51 articles.

1. Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success

2. Direct α-Functionalization of Saturated Cyclic Amines

3. Direct sp3C–H bond activation adjacent to nitrogen in heterocycles

4. Synthesis of Saturated N-Heterocycles

5. Ligand-controlled β-selective C(sp3)–H arylation of N-Boc-piperidines

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