93668-71-4Relevant articles and documents
One pot synthesis of α-ketoamides from ethylarenes and amines: a metal free difunctionalization strategy
Ramanathan, Mani,Kuo, Chun-Kai,Liu, Shiuh-Tzung
, p. 11446 - 11453 (2016)
One-pot and metal free synthesis of α-ketoamides has been described through in situ generation of aryl ketones from easily available ethylarenes followed by amidation with various amines. This multiple oxidation protocol involves catalytic I2-pyridine-TBHP (t-butyl hydroperoxide) mediated oxidative benzylic carbonylation and sequential NaI-TBHP mediated oxidative amidation without using any solvent.
Thromboxane synthetase inhibitors and antihypertensive agents. 1. N-[(1H-imidazol-1-yl)alkyl]aryl amides and N-[(1H-1,2,4-triazol-1-yl)alkyl]aryl amides
Wright Jr.,Press,Chan,Marsico,Haug,Lucas,Tauber,Tomcufcik
, p. 523 - 530 (2007/10/02)
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