147878-14-6Relevant articles and documents
Reactions of thioamides and selenoamides with hydrazonoyl chlorides under phase-transfer conditions. A convenient method of preparation of Δ2-1,3,4-thiadiazolines and Δ2-1,3,4-selenadiazolines
Petrov,Abramov
, p. 331 - 343 (1998)
Reactions of enolizable thio- and selenoamides with hydrazonoyl chlorides in the presence of bases and phase-transfer catalysts result in 2-dialkylamino-Δ2-1,3,4-thia- and selenadiazolines. The reactions proceed through formation of correspondi
α,β-UNSATURATED THIOLATES AND THEIR ANALOGS IN CYCLOADDITION REACTIONS. XVIII. REACTION OF ENOLIZED DIALKYLSELENAMIDES WITH NITRILE IMINES IN THE PRESENCE OF BASES
Abramov, M. A.,Galishev, V. A.,Petrov, M. L.
, p. 1795 - 1804 (2007/10/02)
In reactions with nitrile imines in the presence of bases dialkylselenamides, which are capable of enolization, form derivatives of the five-membered heterocycles 1,3,4-selenadiazolines and not 1,3,4-selenadiazines as supposed earlier.It was established b