103517-58-4Relevant articles and documents
Copper-catalyzed regioselective 2-amination of o-haloanilides with aqueous ammonia
Tang, Yan-Ling,Li, Mei-Ling,Gao, Jin-Chun,Sun, Yun,Qu, Lu,Huang, Feng,Mao, Ze-Wei
supporting information, (2021/04/02)
An efficient Cu(II)-vasicine catalytic system has been developed for intramolecular C[sbnd]N bond formation. In this way, regioselective 2-amination of o-haloanilides with aqueous ammonia in EtOH has been achieved. This strategy provides several advantages, such as good regioselectivity, high yields and functional group tolerance.
Facile synthesis of thiazoles via an intramolecular thia-Michael strategy
Sasmal, Pradip K.,Sridhar,Iqbal, Javed
, p. 8661 - 8665 (2007/10/03)
A mild and efficient method for the synthesis of substituted thiazoles is reported via one-pot N-desilylation, thioacylation/oxythioacylation/thiothioacylation followed by thia-Michael cycloisomerisation. This method has a general applicability to introdu