Synthesis of 1,1,3-Polyfunctionalized Cyclobutane Derivatives from the Reaction of Sulfur Ylides with Bicyclo[1.1.0]butanes

1,1,3-Polyfunctionalized cyclobutane derivatives have been synthesized from sulfur ylides and bicyclo[1.1.0]butanes (BCBs). This protocol operates under mild reaction conditions without the need for catalysts, generally producing moderate to good yields of <i>syn</i>-addition derivatives with structural diversity. An unexpected intramolecular rearrangement mechanism has also been proposed.

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Publication Details

Journal
Organic Letters
Published
2024-08-29
DOI
https://doi.org/10.1021/acs.orglett.4c02388
Citations
7
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.75

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article

Synthesis of 1,1,3-Polyfunctionalized Cyclobutane Derivatives from the Reaction of Sulfur Ylides with Bicyclo[1.1.0]butanes

Huajian Zhu, Jiaan Shao, Linghui Zeng, Chong Zhang et al.
7 citations
Organic Letters
Cyclopropane Reaction Mechanisms
1.75
article

Synthesis of 1,1,3-Polyfunctionalized Cyclobutane Derivatives from the Reaction of Sulfur Ylides with Bicyclo[1.1.0]butanes

Huajian Zhu, Jiaan Shao, Linghui Zeng, Chong Zhang, Chaowei Xiang, Fang Luo, Jiankang Zhang, Ruoyu He, Jing Wang
article en
7 citations

Abstract

1,1,3-Polyfunctionalized cyclobutane derivatives have been synthesized from sulfur ylides and bicyclo[1.1.0]butanes (BCBs). This protocol operates under mild reaction conditions without the need for catalysts, generally producing moderate to good yields of <i>syn</i>-addition derivatives with structural diversity. An unexpected intramolecular rearrangement mechanism has also been proposed.

Organic LettersVol. 26(36)
Hangzhou Xixi hospital (CN), Hangzhou City University, Zhejiang University (CN)
Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 16%
Cyclopropane Reaction Mechanisms
1.75
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Synthesis of 1,1,3-Polyfunctionalized Cyclobutane Derivatives from the Reaction of Sulfur Ylides with Bicyclo[1.1.0]butanes — Huajian Zhu, Jiaan Shao, et al. · Organic Letters (2024) | TGRS Research Map | TGRS