77815-67-9Relevant academic research and scientific papers
Hydrothiolation of unactivated alkynes catalyzed by indium(III) bromide
Yadav,Reddy, B. V. Subba,Raju,Ravindar,Baishya, Gakul
, p. 1474 - 1475 (2007)
Indium(III) bromide is found to catalyze efficiently the hydrothiolation of unactivated alkynes with various thiols under mild conditions to produce the corresponding dithioacetals in excellent yields. However, addition of aromatic thiols on aromatic alky
Synthesis of Alkenes via Peterson Reaction
Ager, David J.
, p. 183 - 194 (2007/10/02)
The α-phenylthiosilanes (2) have been used to prepare the α-silyl anions (1) by reaction with lithium naphthalenide; subsequent condensation with a carbonyl compound gave the alkene (8) via the Peterson reaction.The α-phenylthiosilanes (2) were prepared from n,n-bis(phenylthio)acetals (4) by reaction with lithium naphthalenide and chlorotrimethylsilane.The n,n-bis(phenylthio)acetals (4) were obtained, in turn, from 1,1-bis(phenylthio)acetals (5) by anion formation with butyl-lithium-N,N,N',N'-tetramethylethylenediamine complex in hexane followed by reaction with an alkyl halide.The Peterson reaction was also used to prepare vinyl sulphides (9) and vinyl sulphones (13).
ALKYLATIONS OF BIS(PHENYLTHIO)ACETALS
Ager, David J.
, p. 4763 - 4766 (2007/10/02)
Bis(phenylthio)acetals can be lithiated with n-butyllithium - N,N,N'N'-tetramethylethylenediamine complex in hexane and consequently alkylated.
