676146-66-0Relevant articles and documents
Zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides: A new approach to the synthesis of amidines
Hajibabaei, Khadijeh,Zali-Boeini, Hassan
, p. 2044 - 2048 (2014)
The first zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides is described. Various thioamides were reacted with N-arylsulfonyl aziridines in the presence of a catalytic amount of dry zinc chloride to provide the corresponding
Highly efficient synthesis of thioesters in water
Boeini, Hassan Zali,Kashan, Maryam Eshghi
experimental part, p. 1987 - 1991 (2010/07/04)
Thioesters were efficiently prepared via the direct reaction of tertiary thioamides and alkyl halides in water, and in the presence of catalytic amounts of NaI, hexadecyltrimethylammonium bromide (HTAB), and 1,4-diazabicyclo[2.2.2] octane (DABCO). Hence,