《Synthesis of unsymmetrical disulfides via PPh3-mediated reductive coupling of thiophenols with sulfonyl chlorides》 was written by Wang, Dungai; Liang, Xiao; Xiong, Mingteng; Zhu, Heping; Zhou, Yifeng; Pan, Yuanjiang. Recommanded Product: 98-60-2This research focused onunsym disulfide preparation; thiophenol aryl sulfonyl chloride reductive coupling triphenylphosphine mediated. The article conveys some information:
A facile and rapid synthesis of unsym. aryl disulfides R1-S-S-R2 [R1 = 4-MeC6H4, 4-FC6H4, 2-naphthyl, etc.; R2 = 4-MeOC6H4, 2-NCC6H44, 4-ClC6H4, etc.] using PPh3-mediated reductive coupling of thiophenols with aryl sulfonyl chlorides under catalyst- and base-free conditions in moderate to excellent isolated yields was described. Good functional group tolerance and scalability were achieved in this strategy. The experimental process involved the reaction of 4-Chlorobenzenesulfonyl chloride(cas: 98-60-2Recommanded Product: 98-60-2)
4-Chlorobenzenesulfonyl chloride(cas: 98-60-2) belongs to organochlorine compounds. Many organochlorine compounds have been isolated from natural sources ranging from bacteria to humans. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Recommanded Product: 98-60-2
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics