3,4-Dihydroquinazolines and Quinazolines were prepared starting from N'-aryl-N- (triphenylphosphoranilidene)-carboximidamides and aliphatic or aromatic aldehydes. The mechanism of the reaction is discussed.
A convenient synthesis of quinazoline ring by tandem aza-Wittig reaction/electrocyclic ring closure / E. Rossi, D. Calabrese, F. Farma. - In: TETRAHEDRON. - ISSN 0040-4020. - 47:30(1991), pp. 5819-5834. [10.1016/S0040-4020(01)86532-7]
A convenient synthesis of quinazoline ring by tandem aza-Wittig reaction/electrocyclic ring closure
E. RossiPrimo
;
1991
Abstract
3,4-Dihydroquinazolines and Quinazolines were prepared starting from N'-aryl-N- (triphenylphosphoranilidene)-carboximidamides and aliphatic or aromatic aldehydes. The mechanism of the reaction is discussed.
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