89639-61-2Relevant articles and documents
Thioacetate deprotection
-
Sheet 2/2, (2008/06/13)
A method of thioacetate deprotection by providing a compound of the formula R1—S—CO—R2, and reacting the compound with a quaternary ammonium cyanide salt in the presence of a protic solvent in an inert atmosphere to convert the compound to a product of the formula R1—SH. R1 is an organic group in which the bonding to sulfur is through a saturated carbon, and R2 is an aliphatic group.
One pot rapid synthesis of thiols from alcohols under mild conditions
Bandgar,Sadavarte
, p. 908 - 910 (2007/10/03)
Thiols are prepared in high yields from corresponding alcohols using Ph3P, NBS in acetone and followed by addition of polymer supported hydrosulfide under mild condition.