1005500-83-3Relevant articles and documents
Regio- and stereoselective hydrothiolation reactions of ynamides with diphenyldithiophosphinic acid: Straightforward synthesis of ketene N,S-acetal derivatives
Yasui, Hiroto,Yorimitsu, Hideki,Oshima, Koichiro
, p. 40 - 41 (2008/09/20)
Treatment of N-1-alkynyl-N-methylarenesulfonamides with diphenyldithiophosphinic acid resulted in hydrothiolation reactions to provide ketene N,S-acetal derivatives regio- and stereoselectively. Copyright
Regio- and stereoselective additions of diphenyldithiophosphinic acid to N-(1-alkynyl)amides and 1-alkynyl sulfides
Kanemura, Shigenari,Kondoh, Azusa,Yasui, Hiroto,Yorimitsu, Hideki,Oshima, Koichiro
experimental part, p. 506 - 514 (2009/04/07)
Treatment of N-(l-alkynyl)amides and 1-alkynyl sulfides with diphenyldithiophosphinic acid affords (E)-ketene N,S-acetals and S.S-acetals, respectively. The addition reactions proceed in syn fashions, which consist of protonation of the electron-rich alkynes and the following nucleophilic addition of diphenyldithiophosphinate anion to the resulting cationic intermediates.