Facile Synthesis of Sulfonyl Chlorides/Bromides from Sulfonyl Hydrazides.

Rongxiang Chen, Shaohong Xu, Fumin Shen, Canran Xu, Kaikai Wang, Zhanyong Wang, Lantao Liu

Abstract read

In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in

1citing papers in PubMed

–field-weighted citation impact

1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

Thiol-Free Sulfenylation Redefined: A Single-Atom Transfer Pathway to Symmetrical Di(hetero)arylthioethers via B(CJournal of the American Chemical Society · 2026
Article

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5 · Who and what money

Authors and funding

7 authors.

Rongxiang ChenSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.

Shaohong XuSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.

Fumin ShenSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.

Canran XuSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.

Kaikai WangSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.ORCID 0000-0002-6107-1019

Zhanyong WangSchool of Pharmacy, Xinxiang University, Xinxiang 453000, China.

Lantao LiuCollege of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.

Funding

National Natural Science Foundation of China 21572126National Natural Science Foundation of China 21801214Natural Science Foundation of Henan 202300410016the Higher Educa- 180 tion Institution Key Research Project Plan of Henan Province of China 20B150019the Science and Technology Research Plan Project of Henan Province 202102210224

6 · The paper itself

Abstract

A simple and rapid method for efficient synthesis of sulfonyl chlorides/bromides from sulfonyl hydrazide with NXS (X = Cl or Br) and late-stage conversion to several other functional groups was described. A variety of nucleophiles could be engaged in this transformation, thus permitting the synthesis of complex sulfonamides and sulfonates. In most cases, these reactions are highly selective, simple, and clean, affording products at excellent yields.

Indexed as

NBSNCSsulfonyl bromidessulfonyl chloridessulfonyl hydrazides

Identifiers

PMID34577023

DOI10.3390/molecules26185551

PMCPMC8471771

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