Accéder au contenu
Merck
  • 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
RÉSUMÉ

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.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Chlorure de fer(III) hexahydrate, ACS reagent, 97%
Sigma-Aldrich
Chlorure de fer(III) hexahydrate, reagent grade, ≥98%, chunks
Sigma-Aldrich
Chlorure de fer(III) hexahydrate, puriss. p.a., reag. Ph. Eur., ≥99%
Sigma-Aldrich
Chlorure de fer(III) hexahydrate, puriss. p.a., ACS reagent, crystallized, 98.0-102% (RT)
Sigma-Aldrich
Iron(III) chloride, sublimed grade, ≥99.9% trace metals basis
Sigma-Aldrich
Iron(III) chloride, anhydrous, powder, ≥99.99% trace metals basis
Sigma-Aldrich
Iron(III) chloride solution, purum, 45% FeCl3 basis
Sigma-Aldrich
Iron(III) chloride solution, 0.2 M in 2-methyltetrahydrofuran
Millipore
TDA Reagent, suitable for microbiology