87514-04-3Relevant articles and documents
A facile stereoselective synthesis of (E)-α-silylyinyl sulfides via hydromagnesiation of alkynylsilanes
Cai, Mingzhong,Xia, Jim,Wang, Pingping
, p. 644 - 647 (2005)
Hydromagnesiation of alkynylsilanes 1 in diethyl ether gave (Z)-α-silylvinyl Grignard reagents 2, which reacted with arylsulfenyl chlorides 3 to afford stereoselectively (E)-α-silylvinyl sulfides 4 in good yields. (E)-α-Silylvinyl sulfides 4 could undergo
Stereo-recognizing transformation of (E)-alkenyl halides into sulfides catalyzed by nickel(0) triethyl phosphite complex
Yatsumonji, Yasutaka,Okada, Orie,Tsubouchi, Akira,Takeda, Takeshi
, p. 9981 - 9987 (2007/10/03)
(E)-Alkenyl halides were transformed into (E)-alkenyl sulfides by the nickel(0) triethyl phosphite complex-catalyzed reaction with thiols, whereas (Z)-alkenyl halides gave alkynes under the same reaction conditions. Aryl halides were also transformed into aryl sulfides using the same reagent system.