139474-21-8Relevant articles and documents
A facile synthesis of N-arylcyanoformamidoximes, 4-aryl-3-cyano-1,2,4- oxadiazin-5(6H)-ones, 2-cyanoquinazolin-3-oxides, and 2-cyanoquinazolines via 5-arylimino-4-chloro-5H-1,2,3-dithiazoles
Chang, Yong-Goo,Kim, Kyongtae
, p. 2653 - 2666 (2007/10/03)
The reaction of 5-arylimino-4-chloro-5H-1,2,3-dithiazoles with hydroxylamine hydrochloride in pyridine at room temperature gave N- arylcyanoformamidoximes, which were utilized as starting materials for the synthesis of 4-alkyl- (or aryl)-2-cyanoquinazolines and 4-aryl-3-cyano-1,2,4- oxadiazin-5(6H)-ones.
HAMMETT-TAFT CONSTANTS OF SUBSTITUTED 2- AND 4-QUINAZOLINYL GROUPS
Baram, S. G.,Shkurko, O. P.,Mamaev, V. P.
, p. 601 - 605 (2007/10/02)
From the chemical shifts of the meta- and para-carbon atoms of the phenyl group in phenylquinazolines the ?I and ?R0 constants of 2- and 4-quinazolinyl groups were determined.Correlation equations which enable us to calcul