Catalytic Enantioselective Formal (3 + 3) Cycloaddition of 3-Halooxindoles with Pyridinium 1,4-Zwitterionic Thiolates

. The products could be further converted to chiral 3-sulfenyl-3,3'-disubstituted oxindoles with stereoretention. This work also represents the first report on a catalytic asymmetric cycloaddition reaction involving pyridinium 1,4-zwitterionic thiolates.

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Publication Details

Journal
Organic Letters
Published
2026-03-31
DOI
https://doi.org/10.1021/acs.orglett.6c00614
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalytic Enantioselective Formal (3 + 3) Cycloaddition of 3-Halooxindoles with Pyridinium 1,4-Zwitterionic Thiolates

Ming‐Qiang Zhou, Yong You, Ting-Jia Sun, Yingyue Zhang et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Catalytic Enantioselective Formal (3 + 3) Cycloaddition of 3-Halooxindoles with Pyridinium 1,4-Zwitterionic Thiolates

Ming‐Qiang Zhou, Yong You, Ting-Jia Sun, Yingyue Zhang, Xue-Song Peng, Guo-Yin Sun, Wei Sun, Jian-Qiang Zhao, Wei-Cheng Yuan
article en

Abstract

. The products could be further converted to chiral 3-sulfenyl-3,3'-disubstituted oxindoles with stereoretention. This work also represents the first report on a catalytic asymmetric cycloaddition reaction involving pyridinium 1,4-zwitterionic thiolates.

Organic LettersVol. 28(14)
Chinese Academy of Sciences (CN), Chengdu Organic Chemicals (China) (CN), Innovation Research Center (US), Chengdu University (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Department of Science and Technology of Sichuan Province
Openalex Percentile: Top 31%
Catalytic C–H Functionalization Methods
DOISourceOpenAlex
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