Silver catalysed asymmetric [3+2] cycloaddition for the construction of 5−5-membered 1,3'-indolyl pyrrole atropisomers

An atropoenantioselective Ag-catalysed [3+2] cycloaddition of N-alkynyl ketones with isocyanides has been developed to access 5−5-membered 1,3'-indolyl pyrroles bearing C-N axial chirality in high yields and excellent enantioselectivities. The resulting...

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Publication Details

Journal
Chemical Communications
Published
2026-01-01
DOI
https://doi.org/10.1039/d6cc00517a
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.00
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article

Silver catalysed asymmetric [3+2] cycloaddition for the construction of 5−5-membered 1,3'-indolyl pyrrole atropisomers

Jinzhong Yao, Yan Xie, Weihui Zhong, Zhengguo Deng et al.
Chemical Communications
Axial and Atropisomeric Chirality Synthesis
article

Silver catalysed asymmetric [3+2] cycloaddition for the construction of 5−5-membered 1,3'-indolyl pyrrole atropisomers

Jinzhong Yao, Yan Xie, Weihui Zhong, Zhengguo Deng, Jiayang Lv, Fei Ling, Xinyu Chen, Chao Xiong
article en

Abstract

An atropoenantioselective Ag-catalysed [3+2] cycloaddition of N-alkynyl ketones with isocyanides has been developed to access 5−5-membered 1,3'-indolyl pyrroles bearing C-N axial chirality in high yields and excellent enantioselectivities. The resulting...

Chemical Communications
Openalex Percentile: Top 7%
Axial and Atropisomeric Chirality Synthesis
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Silver catalysed asymmetric [3+2] cycloaddition for the construction of 5−5-membered 1,3'-indolyl pyrrole atropisomers — Jinzhong Yao, Yan Xie, et al. · Chemical Communications (2026) | TGRS Research Map | TGRS