51137-49-6Relevant academic research and scientific papers
Sequential N-acylamide methylenation-enamide ring-closing metathesis: A synthetic entry to 1,4-dihydroquinolines
Bennasar, M.-Llu?sa,Roca, Tomàs,Monerris, Manuel,García-Díaz, Davinia
, p. 4035 - 4038 (2007/10/03)
A new synthetic entry to the 1,4-dihydroquinoline nucleus is reported. The procedure involves the dimethyltitanocene methylenation of N-(alkoxycarbonyl) amides derived from 2-allylanilines, followed by ring-closing metathesis of the resulting enamides.
ACYLATION OF SCHIFF BASES WITH METHYL CHLOROCARBONATE
Mochalin, V. B.,Rogozin, K. I.
, p. 1268 - 1270 (2007/10/02)
N-Substituted N-alkenylcarbamates are formed in the reaction of Schiff bases, obtained from aldehydes and ketones, with methyl chlorocarbonate in the presence of diethylaniline.
