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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
ZUSAMMENFASSUNG

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.

MATERIALIEN
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Marke
Produktbeschreibung

Sigma-Aldrich
Eisen(III)-chlorid Hexahydrat, ACS reagent, 97%
Sigma-Aldrich
Eisen(III)-chlorid Hexahydrat, reagent grade, ≥98%, chunks
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Eisen(III)-chlorid Hexahydrat, puriss. p.a., ACS reagent, crystallized, 98.0-102% (RT)
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Eisen(III)-chlorid, sublimed grade, ≥99.9% trace metals basis
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Eisen(III)-chlorid, anhydrous, powder, ≥99.99% trace metals basis
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Eisen(III)-chlorid -Lösung, purum, 45% FeCl3 basis
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Eisen(III)-chlorid, 0.2 M in 2-methyltetrahydrofuran
Millipore
TDA-Reagenz, suitable for microbiology