The 6- and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinones I [R = H, R1 = Me, RR1 = (CH2)4] were acylated to give 1-acylpyrimidine derivs. II [R2 = Ph, p-MeOC6H4 3,4-(methylenedioxy)phenyl] under Friedel-Craft-like conditions. In different acylation conditions 4-(acyloxy)pyrimidines were also obtained. II [R2 = 3,4-(methylenedioxy)phenyl] were converted into 1-acylisouridine analogs III.

6-Alkyl-2-methoxy-4(3H)-pyrimidinone and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinone in the transformations of pyrimidines - regiospecific 1-N-acylation of pyrimidines / M., Botta; F., De Angelis; G., Finizia; R., Nicoletti; Delfini, Maurizio. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - STAMPA. - 26:28(1985), pp. 3345-3348. [10.1016/S0040-4039(00)98294-7]

6-Alkyl-2-methoxy-4(3H)-pyrimidinone and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinone in the transformations of pyrimidines - regiospecific 1-N-acylation of pyrimidines

DELFINI, Maurizio
1985

Abstract

The 6- and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinones I [R = H, R1 = Me, RR1 = (CH2)4] were acylated to give 1-acylpyrimidine derivs. II [R2 = Ph, p-MeOC6H4 3,4-(methylenedioxy)phenyl] under Friedel-Craft-like conditions. In different acylation conditions 4-(acyloxy)pyrimidines were also obtained. II [R2 = 3,4-(methylenedioxy)phenyl] were converted into 1-acylisouridine analogs III.
1985
5; 6-dialkyl-2-methoxy-4(3H)-pyrimidinones; NMR spectroscopy; Friedel-Craft-like conditions
01 Pubblicazione su rivista::01a Articolo in rivista
6-Alkyl-2-methoxy-4(3H)-pyrimidinone and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinone in the transformations of pyrimidines - regiospecific 1-N-acylation of pyrimidines / M., Botta; F., De Angelis; G., Finizia; R., Nicoletti; Delfini, Maurizio. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - STAMPA. - 26:28(1985), pp. 3345-3348. [10.1016/S0040-4039(00)98294-7]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/471891
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