Development of a Strategy for Linear-Selective Cu-Catalyzed Reductive Coupling of Ketones and Allenes for the Synthesis of Chiral γ-Hydroxyaldehyde Equivalents-Reference-Cited by-同舟云学术

Development of a Strategy for Linear-Selective Cu-Catalyzed Reductive Coupling of Ketones and Allenes for the Synthesis of Chiral γ-Hydroxyaldehyde Equivalents

Published:2019-09-18 Issue:19 Volume:21 Page:7992-7998
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Klake Raphael K.¹,Gargaro Samantha L.¹,Gentry Skyler L.¹,Elele Sharon O.¹,Sieber Joshua D.¹^ORCID

Affiliation:

1. Department of Chemistry, Virginia Commonwealth University, 1001 West Main Street, Richmond, Virginia 23284-3028, United States

Funder

Bill and Melinda Gates Foundation

Virginia Commonwealth University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02973

Reference89 articles.

1. Recent Developments in Asymmetric Hydrogenation and Transfer Hydrogenation of Ketones and Imines through Dynamic Kinetic Resolution

2. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones

3. The role of the metal-bound N–H functionality in Noyori-type molecular catalysts

4. Rhodium-Catalyzed Asymmetric Arylation

5. Recent Advances in Catalytic Asymmetric Synthesis of Tertiary Alcohols via Nucleophilic Addition to Ketones

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