Catalytic asymmetric aromatizing inverse electron-demand [4+2] cycloaddition of 1-thioaurones and 1-azaaurones-Reference-Cited by-同舟云学术

Catalytic asymmetric aromatizing inverse electron-demand [4+2] cycloaddition of 1-thioaurones and 1-azaaurones

Published:2022 Issue:4 Volume:58 Page:553-556
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yuan Shu-Pei¹²³,Dou Pei-Hao¹²³,Jia Yun-Qing¹²³,Zhao Jian-Qiang²^ORCID,You Yong²^ORCID,Wang Zhen-Hua²^ORCID,Zhou Ming-Qiang¹,Yuan Wei-Cheng¹²^ORCID

Affiliation:

1. National Engineering Research Center of Chiral Drugs, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China

2. Innovation Research Center of Chiral Drugs, Institute for Advanced Study, Chengdu University, Chengdu 610106, China

3. University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

An organocatalytic asymmetric aromatizing inverse electron-demand [4+2] cycloaddition of 1-thioaurones/1-azaaurones with γ-deconjugated butenolides and azlactones was developed.

Funder

National Natural Science Foundation of China

Department of Science and Technology of Sichuan Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D1CC06357J

Reference40 articles.

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2. Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles

3. Inverse electron demand Diels–Alder (iEDDA)-initiated conjugation: a (high) potential click chemistry scheme

4. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

5. Asymmetric Induction via a Helically Chiral Anion: Enantioselective Pentacarboxycyclopentadiene Brønsted Acid-Catalyzed Inverse-Electron-Demand Diels–Alder Cycloaddition of Oxocarbenium Ions

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