The reactivity of 1-aryl-4-dimethylamino-2-phenyl-1,3-diaza-1,3-butadienes (1) towards dienophiles, 1,3-dipoles and C-nucleophiles was investigated. N-Phenylmethylene-benzenesulfonamide (2), phenylisocyanate (6), C,N-diphenylnitrone (9) and acylacetates (10) reacted with 1 giving quinazoline or pyrimidine derivatives. The possible mechanisms involved in products formation are discussed.
Reactivity of 1-aryl-4-dimethylamino-2-phenyl-1,3-diaza-1,3-butadienes towards dienophiles, 1,3-dipoles and carbanions / P. Dalla Croce, R. Ferraccioli, C. La Rosa. - In: HETEROCYCLES. - ISSN 0385-5414. - 45:7(1997), pp. 1309-1318.
Reactivity of 1-aryl-4-dimethylamino-2-phenyl-1,3-diaza-1,3-butadienes towards dienophiles, 1,3-dipoles and carbanions
P. Dalla CrocePrimo
;C. La RosaUltimo
1997
Abstract
The reactivity of 1-aryl-4-dimethylamino-2-phenyl-1,3-diaza-1,3-butadienes (1) towards dienophiles, 1,3-dipoles and C-nucleophiles was investigated. N-Phenylmethylene-benzenesulfonamide (2), phenylisocyanate (6), C,N-diphenylnitrone (9) and acylacetates (10) reacted with 1 giving quinazoline or pyrimidine derivatives. The possible mechanisms involved in products formation are discussed.File in questo prodotto:
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