A General, Scalable, Organocatalytic Nitro-Michael Addition to Enones: Enantioselective Access to All-Carbon Quaternary Stereocenters-Reference-Cited by-同舟云学术

A General, Scalable, Organocatalytic Nitro-Michael Addition to Enones: Enantioselective Access to All-Carbon Quaternary Stereocenters

Published:2015-03-11 Issue:6 Volume:17 Page:1505-1508
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Gu Xiaodong¹,Dai Yuanyuan¹,Guo Tingting¹,Franchino Allegra²,Dixon Darren J.²,Ye Jinxing¹

Affiliation:

1. Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

2. Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, United Kingdom

Funder

Program for New Century Excellent Talents in University

Ministry of Education of the People's Republic of China

Shanghai Municipal Education Commission

European Commission Directorate-General for Research and Innovation

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00387

Reference54 articles.

1. Asymmetric creation of quaternary carbon centers

2. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters

3. Stereoselective formation of quaternary carbon centers and related functions

4. Asymmetric Catalysis Special Feature Part I: Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

5. Stereoselective Construction of Quaternary Stereocenters

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