74457-62-8Relevant articles and documents
Efficient synthesis of 2-aminothiazole-4-phenyl-5-acetamides via the open chain tautomers of γ-keto amides
Tsolomiti, Georgia,Tsolomitis, Athanase
, p. 501 - 507 (2007/10/03)
A simple and efficient method is described for the synthesis of new functionalized 2-aminothiazoles, the 2-aminothiazole-4-phenyl-5-acetamides 5, in 67-96% yields based on an application of the Hantzsch synthesis. The method involves the reaction of thiou
AN ALTERNATIVE ROUTE TO 4-BENZOYL-2-AZETIDINONES
Abdulla, Riaz F.,Williams, James C.
, p. 997 - 1000 (2007/10/02)
Cyclodehydrohalogenation by terminal N1-C4 bond formation affords N-aryl-4-benzoyl-2-azetidinones from 3-benzoyl-3-bromopropionanilides in an unequivocal annelation process.