82782-22-7Relevant academic research and scientific papers
Synthesis of vinyl sulfides under base-free conditions using selenium ionic liquid
Thurow, Samuel,Ostosi, Naiana T.,Mendes, Samuel R.,Jacob, Raquel G.,Lenard?o, Eder J.
experimental part, p. 2651 - 2653 (2012/06/30)
A very simple procedure is described for the efficient synthesis of vinyl sulfides by hydrothiolation of terminal alkynes using 1-n-butyl-3- methylimidazolium methylselenite, [bmim][SeO2(OCH3)]. The reaction proceeds cleanly under mi
Mass Spectral Rearrangements of N-(4'-Arylthio-2'-butynyl)-N-(2"-arylthio-2"-propenyl)-p-toluidines, N,N-Bis(2'-arylthio-2'-propenyl)-p-toluidines and 1,2-Bis(arylthio)acenaphthenes
Glaspy, P. E.,Hancock, R. A.,Thyagarajan, B. S.
, p. 228 - 235 (2007/10/02)
Under electron impact the title compounds display, in addition to the sequential loss of the arylthio groups, the elimination of a bisaryl disulphide moiety, but they do not eliminate sulphur.The behaviour of the p-toluidine derivatives supports the rearr
DIRECTION OF NUCLEOPHILIC ADDITION OF ARENETHIOLS TO ACETYLENIC ALCOHOLS
Dzhafarov, A. A.,Aslanov, I. A.,Trofimov, B. A.,Ibadzade, A. K.,Ibragimov, N. Yu.
, p. 643 - 646 (2007/10/02)
2-Arylthio-2-propen-1-ols and 3-arylthio-2-propen-1-ols (E and Z isomers),i.e., the products from addition according to and against the Markovnikov rule, were synthesized by the reaction of arenethiols with acetylenic alcohols.The prototropic rearrangemen
