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Merck

Disulfide formation via sulfenamides.

Chemical communications (Cambridge, England) (2010-08-24)
Jia Pan, Ming Xian
要旨

A phosphine-mediated one-step disulfide formation from S-nitrosothiols has been developed. This reaction can convert unstable S-nitrosothiols to stable disulfides via sulfenamide intermediates under very mild conditions. It has the potential to be used for the detection of S-nitrosothiols.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
スルファメラジン, ReagentPlus®, ≥99.0%
Supelco
スルファメラジン, VETRANAL®, analytical standard