Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition-Reference-Cited by-同舟云学术

Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition

Published:2019 Issue:10 Volume:6 Page:1567-1571
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Li Boyu¹²³⁴⁵^ORCID,Gao Fengyun¹²³⁴⁵,Feng Xing¹²³⁴⁵,Sun Mengmeng¹²³⁴⁵,Guo Yifei¹²³⁴⁵,Wen Dongwa¹²³⁴⁵,Deng Yabo¹²³⁴⁵,Huang Jinqi⁶⁷⁸⁹¹⁰,Wang Kairong¹²³⁴⁵,Yan Wenjin¹²³⁴⁵^ORCID

Affiliation:

1. The Institute of Pharmacology

2. Key Laboratory of Preclinical Study for New Drugs of Gansu Province

3. School of Basic Medical Sciences

4. Lanzhou University

5. Lanzhou 730000

6. Key Laboratory for Cancer T-Cell Theranostics and Clinical Translation (CTCTCT) & Translational Medicine Research Center (TMRC)

7. Institute of Biomedical Research

8. School of Pharmaceutical Sciences

9. Xiamen University

10. Xiamen 361102

Abstract

The first organocatalyzed [3 + 2] cyclisation of N-2,2,2-trifluoroethylisatin ketimines with aurones has been developed.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C9QO00241C

Reference49 articles.

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2. Catalytic Asymmetric Synthesis of Chiral Benzofuranones

3. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

4. Bioactive Benzofuran derivatives: A review

5. Synthesis of Heterocycles Mediated by Benzotriazole. 2. Bicyclic Systems

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