Enantioselective Michael Addition of Photogenerated o-Quinodimethanes to Enones Catalyzed by Chiral Amino Acid Esters-Reference-Cited by-同舟云学术

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Enantioselective Michael Addition of Photogenerated o-Quinodimethanes to Enones Catalyzed by Chiral Amino Acid Esters

Published:2017-04-26 Issue:9 Volume:19 Page:2322-2325
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yuan Xiaoqian¹,Dong Shupeng¹,Liu Zhen¹,Wu Guibing¹,Zou Chuncheng¹,Ye Jinxing¹^ORCID

Affiliation:

1. Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education; Shanghai Key Laboratory of New Drug Design, School of Pharmacy, ‡State Key Laboratory of Chemical Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

Funder

Program for New Century Excellent Talents in University

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.7b00862

Reference65 articles.

1. STEREOSPECIFICITY IN A NEW TYPE OF SYNTHETIC ANTITUBERCULOUS AGENT1,2

2. Photoenolisation

3. A rotation-controlled excited-state reaction. The photoenolization of ortho alkyl phenyl ketones

4. The Photoenolization of 2-Methylacetophenone and Related Compounds

5. The formation of two photoenols via a common pathway in the photochemistry of 2-methylbenzophenone

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3. Iridium‐Catalyzed Asymmetric Allylic Benzylation with Photogenerated Hydroxy‐ o ‐Quinodimethanes;Angewandte Chemie International Edition;2022-10-25

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