Sulphur ylide-mediated cyclopropanation and subsequent spirocyclopropane rearrangement reactions-Reference-Cited by-同舟云学术

Sulphur ylide-mediated cyclopropanation and subsequent spirocyclopropane rearrangement reactions

Published:2022 Issue:17 Volume:20 Page:3486-3490
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Dai Qing-Song¹²³,Li Jun-Long⁴²^ORCID,Wang Qi-Wei¹⁴²,Yang Si-Lin²,Tao Ying-Mao²,He Mei-Hao²,Li Qing-Zhu⁴²,Han Bo⁵⁴^ORCID,Zhang Xiang⁴²

Affiliation:

1. Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China

2. Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province, Sichuan Industrial Institute of Antibiotics, School of Pharmacy, Chengdu University, Chengdu 610106, PR China

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

4. Institute for Advanced Study, Chengdu University, Chengdu 610106, China

5. State Key Laboratory of Southwestern Chinese Medicine Resources, Hospital of Chengdu University of Traditional Chinese Medicine, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China

Abstract

A formal (2 + 1) annulation and three-component (1 + 1 + 1) cascade cyclisation via sulphur ylide cyclopropanation under mild conditions is described, with the spiro-cyclopropyl iminoindoline moiety transformed into pyrrolo[3,4-c]quinoline through a novel rearrangement process.

Funder

National Natural Science Foundation of China

Department of Science and Technology of Sichuan Province

Chengdu University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00466F

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