24585-93-1Relevant articles and documents
Selective Oxidative Cleavage of 3-Methylindoles with Primary Amines Affording Quinazolinones
He, Junhui,Dong, Jianyu,Su, Lebin,Wu, Shaofeng,Liu, Lixin,Yin, Shuang-Feng,Zhou, Yongbo
, p. 2522 - 2526 (2020/04/09)
A selective functionalization of C-C-C bonds toward N-C-O bonds is realized by an n-Bu4NI-catalyzed reaction of 3-methylindoles with primary amines using TBHP as the unique oxidant. The systematic process involves oxygenation, nitrogenation, ring-opening, and recyclization, affording a broad range of quinazolinones in good to excellent yields.
NMR studies of 3-substituted quinazolin-4(3H)-ones
Georgescu, Florentina,Georgescu,Caproiu, Miron T.,Draghici, Constantin
, p. 341 - 350 (2007/10/03)
3-Phenacyl-, 3-methylnaphthoyl-, 3-methylphenacyl- and 3-benzylquinazolin-4(3H)-one derivatives were synthesized and their 1H-NMR, 13C-NMR spectra were recorded. The chemical shifts and the coupling constants are reported.