Control of Activation Mode To Achieve Diastereodivergence in Asymmetric Syntheses of Chiral Spiropiperidinone Derivatives-Reference-Cited by-同舟云学术

Control of Activation Mode To Achieve Diastereodivergence in Asymmetric Syntheses of Chiral Spiropiperidinone Derivatives

Published:2016-12-20 Issue:1 Volume:82 Page:397-406
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Xiang¹,Huang Wei¹,Liu Yan-Qing¹,Kang Jing-Wen¹,Xia Dan¹,He Gu²,Peng Cheng¹,Han Bo¹^ORCID

Affiliation:

1. State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, People’s Republic of China

2. State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, People’s Republic of China

Funder

Foundation for the Author of National Excellent Doctoral Dissertation of the People's Republic of China

Department of Science and Technology of Sichuan Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02489

Reference74 articles.

1. Dual Catalysis Becomes Diastereodivergent

2. Asymmetric Synthesis of 3,4-Diaminochroman-2-ones Promoted by Guanidine and Bisguanidium Salt

3. Stereodivergence in Amine-Catalyzed Regioselective [4 + 2] Cycloadditions of β-Substituted Cyclic Enones and Polyconjugated Malononitriles

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