Trimethylindolenines as C–N synthons for the assembly of spiro[oxindole-thioxoimidazolidine-indoline] hybrids in formal [3+2] cycloadditions-Reference-Cited by-同舟云学术

Trimethylindolenines as C–N synthons for the assembly of spiro[oxindole-thioxoimidazolidine-indoline] hybrids in formal [3+2] cycloadditions

Published:2023 Issue:26 Volume:47 Page:12296-12303
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Zhang Wen-Hui¹,Chen Zi-Yue²,Liu Ren-Ming²,Liu Xiong-Wei¹,Pan Bo-Wen¹,Zhou Jian³^ORCID,Zhou Ying¹,Tian You-Ping¹,Liu Xiong-Li¹²^ORCID

Affiliation:

1. College of Pharmaceutical Sciences, Guizhou University of Traditional Chinese Medicine, Guiyang, 550025, China

2. National & Local Joint Engineering Research Center for the Exploition of Homology Resources of Southwest Medicine and Food, Guizhou University, Guiyang 550025, Guizhou, China

3. Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, East China Normal University, Shanghai 200062, P. R. China

Abstract

This is the first example of trimethylindolenines serving as useful C–N synthons in [3+2] cycloaddition reactions.

Funder

Data Center of Management Science, National Natural Science Foundation of China - Peking University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ00901G

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