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Auteurs principaux: Zhang, Zhaoqing, Zhang, Xinping, Jia, Runyu, Jia, Tiezheng
Format: Artículo científico
Langue:en
Publié: The Journal of organic chemistry 2025
Accès en ligne:https://pubmed.ncbi.nlm.nih.gov/40611558/
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author Zhang, Zhaoqing
Zhang, Xinping
Jia, Runyu
Jia, Tiezheng
author_facet Zhang, Zhaoqing
Zhang, Xinping
Jia, Runyu
Jia, Tiezheng
Zhang, Zhaoqing
Zhang, Xinping
Jia, Runyu
Jia, Tiezheng
collection PubMed - marine biology
contents Synthesis of Alkyl (-Benzyl)-Aryl Sulfoxides Enabled by Truce-Smiles Rearrangement. Zhang, Zhaoqing Zhang, Xinping Jia, Runyu Jia, Tiezheng An atom-economical and chemoselective synthesis of alkyl (-benzyl)-aryl sulfoxides has been developed. Sulfenate anions, which were generated by the Truce-Smiles rearrangement of heteroaryl (-alkyl)-aryl sulfoxides, have been trapped by primary alkyl halides to deliver the corresponding sulfoxides. A Truce-Smiles rearrangement/cyclization cascade has been designed to expand the scope of secondary cycloalkyl sulfoxides.
format Artículo científico
id pubmed_40611558
institution PubMed
language en
publishDate 2025
publisher The Journal of organic chemistry
record_format pubmed
spellingShingle Synthesis of Alkyl (-Benzyl)-Aryl Sulfoxides Enabled by Truce-Smiles Rearrangement.
Zhang, Zhaoqing
Zhang, Xinping
Jia, Runyu
Jia, Tiezheng
Synthesis of Alkyl (-Benzyl)-Aryl Sulfoxides Enabled by Truce-Smiles Rearrangement. Zhang, Zhaoqing Zhang, Xinping Jia, Runyu Jia, Tiezheng An atom-economical and chemoselective synthesis of alkyl (-benzyl)-aryl sulfoxides has been developed. Sulfenate anions, which were generated by the Truce-Smiles rearrangement of heteroaryl (-alkyl)-aryl sulfoxides, have been trapped by primary alkyl halides to deliver the corresponding sulfoxides. A Truce-Smiles rearrangement/cyclization cascade has been designed to expand the scope of secondary cycloalkyl sulfoxides.
title Synthesis of Alkyl (-Benzyl)-Aryl Sulfoxides Enabled by Truce-Smiles Rearrangement.
url https://pubmed.ncbi.nlm.nih.gov/40611558/