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@inproceedings{387151,
author = {Mohamed, Walid Fathalla and Pazdera, Pavel},
address = {Banká Bystrica},
booktitle = {Sborník príspevkov 53. zjazd Chemických spoločností},
edition = {1.},
keywords = {Quinazolines; thioureas; guanidines},
language = {eng},
location = {Banká Bystrica},
isbn = {80-89029-22-1},
pages = {279-280},
publisher = {FPV Univerzita Mateja Bela v Banskej Bystrici},
title = {The reactivity of N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas},
year = {2001}
}
TY - JOUR
ID - 387151
AU - Mohamed, Walid Fathalla - Pazdera, Pavel
PY - 2001
TI - The reactivity of N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas
VL - 1.
PB - FPV Univerzita Mateja Bela v Banskej Bystrici
CY - Banká Bystrica
SN - 8089029221
KW - Quinazolines
KW - thioureas
KW - guanidines
N2 - The model compound N3-aryl-N1-(2-phenyl-3,4-dihydroquinazolin-4-yl)thiourea 1 was synthesized in a Domino reaction of N2-(2-cyanophenyl)-N1-thioxomethylidenebenzene-1-carboximidamide with anilines. This compound reacts with alkyl halides, phenacyl bromides, chloroacetic acid derivatives, amines, amines in the presence of H2O2, amines in the presence of CH2O (under Mannich reaction conditions) and acyl halides to give a variety of compounds. The structure of these products together with the reason for there formation proved by quantum computational studies will be reported in this contribution. Compounds were identified by FTIR, 1H NMR, 13C NMR, X-ray, mass spectroscopy and by the ab initio computational.
ER -
MOHAMED, Walid Fathalla and Pavel PAZDERA. The reactivity of N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas. In \textit{Sborník príspevkov 53. zjazd Chemických spoločností}. 1st ed. Banká Bystrica: FPV Univerzita Mateja Bela v Banskej Bystrici, 2001, p.~279-280. 1. ISBN~80-89029-22-1.
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