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  • Iron halide-mediated regio- and stereoselective halosulfonylation of terminal alkynes with sulfonylhydrazides: synthesis of (E)-β-chloro and bromo vinylsulfones.

Iron halide-mediated regio- and stereoselective halosulfonylation of terminal alkynes with sulfonylhydrazides: synthesis of (E)-β-chloro and bromo vinylsulfones.

The Journal of organic chemistry (2013-08-28)
Xiaoqing Li, Xinhua Shi, Mingwu Fang, Xiangsheng Xu
ABSTRACT

Halosulfonylation of terminal alkynes was achieved with sulfonylhydrazides as the sulfonyl precursor and inexpensive iron halide as halide source in the presence of TBHP, allowing the regio- and stereoselective generation of (E)-β-chloro and bromo vinylsulfones.

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Sigma-Aldrich
Cloruro di ferro(III), ACS reagent, 97%
Sigma-Aldrich
Cloruro di ferro(III), reagent grade, ≥98%, chunks
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Cloruro di ferro(III), puriss. p.a., ACS reagent, crystallized, 98.0-102% (RT)
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Iron(III) chloride, sublimed grade, ≥99.9% trace metals basis
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Iron(III) chloride, anhydrous, powder, ≥99.99% trace metals basis
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Iron(III) chloride solution, purum, 45% FeCl3 basis
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Iron(III) chloride solution, 0.2 M in 2-methyltetrahydrofuran
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TDA Reagent, suitable for microbiology