15148-54-6Relevant articles and documents
A STEREOSELECTIVE ROUTE TO E-3-HYDROXYALKENYL PHENYL SULFIDES
Takano, Seiichi,Sugihara, Yoshiaki,Ogasawara, Kunio
, p. 845 - 846 (1993)
E-3-Hydroxyalkenyl phenyl sulfides are generated stereoselectively when 2,3-epoxyalkyl phenyl sulfides having 3-syn-substituent are exposed to an excess n-butyllithium in THF solution.
Rhodium-catalyzed hydrothiolation of alkynes with thiols for construction of sulfur-containing π-conjugated systems
Yoshimura, Aya,Nomoto, Akihiro,Ogawa, Akiya
, p. 2381 - 2389 (2014/06/24)
To synthesize sulfur-containing π-conjugated polymers, reaction conditions for rhodium-catalyzed hydrothiolation of terminal alkynes with arenethiols are optimized in detail. Under the optimized conditions, rhodium-catalyzed hydrothiolation of terminal al
Synthesis of vinyl sulfides using glycerol as a recyclable solvent
Lenardao, Eder J.,Silva, Marcio S.,Lara, Renata G.,Marczewski, Junior M.,Sachini, Maraisa,Jacob, Raquel G.,Alves, Diego,Perin, Gelson
experimental part, p. 272 - 282 (2011/05/13)
A new, clean, and efficient protocol is described for the hydrothiolation of terminal alkynes promoted by KF/Al2O3, using glycerol as recyclable solvent. This improved method furnishes selectively the corresponding anti-Markovnikov v
