79246-09-6Relevant academic research and scientific papers
Enantioselective Diels-Alder reaction of α-(acylthio)acroleins: A new entry to sulfur-containing chiral quaternary carbons
Sakakura, Akira,Yamada, Hiroki,Ishihara, Kazuaki
supporting information; experimental part, p. 2972 - 2975 (2012/07/28)
A catalytic and enantioselective Diels-Alder reaction of α-(carbamoylthio)acroleins induced by an organoammonium salt of chiral triamine is described. α-(Carbamoylthio)acroleins are designed and synthesized as new sulfur-containing dienophiles for the fir
The Reaction of Dibenzylthiocarbamoyl Chloride with Sodium Nitrite
Nakajima, Masayuki,Herget, Rose Ann,Anselme, Jean-Pierre
, p. 2547 - 2548 (2007/10/02)
The reaction of dibenzylthiocarbamoyl chloride with sodium nitrite in acetonitrile at room temperature yields N-nitrosodibenzylamine, dibenzylcarbamoyl chloride, bis(dibenzylcarbamoyl) disulfide, benzaldehyde, and benzyl isothiocyanate; possible mechanisms for the formation of these products are suggested.
