109480-90-2Relevant academic research and scientific papers
Thiol addition to aryl propargyl alcohols under mild conditions: An accelerating neighboring group effect
See Waters, Marjorie,Cowen, Jennifer A.,McWilliams, J. Christopher,Maligres, Peter E.,Askin, David
, p. 141 - 144 (2007/10/03)
Aryl alkynols provide a convenient entry into α-hydroxyketones via thiol addition followed by hydrolysis. Thiols have been added to several non- activated alkynes under mild, basic conditions. A coordinating functional group in close proximity to the triple bond facilitates this reaction.
S,S-Dialkyl Dithiocarbonates as a Convenient Source of Alkanethiols: an Improved Synthesis of Alkylthiocarboxylic Acids
Cadamuro, Silvano,Degani, Iacopo,Fochi, Rita,Regondi, Valeria
, p. 1070 - 1074 (2007/10/02)
A wide variety of β-alkylthiocarboxylic acids are obtained by addition of alkanethiols - generated in situ from S,S-dialkyl dithiocarbonates - to appropriate α,β-unsaturated carboxylic acids in good to excellent yields.
