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Chromanone synthesis

Chlorobenzenes, sulphur-containing, reactivities of 590, 591 Chloropalladiosulphonylation 172 Chromanones, synthesis of 328 Chromatographic methods for detection and determination 111-113, 119-121... [Pg.1198]

There is little doubt, however, that the carbonyl compound which has been used most with o-hydroxyacetophenone in chromanone synthesis is benzaldehyde. This gives rise to a chalcone which cyclizes in acid or basic media to a flavanone (Scheme 227) (70JOC2286). During the acid-promoted cyclization of 5-acetamidochalcones, concomitant deacetylation occurs and 6-aminoflavanones result (56JOC1408). [Pg.853]


See other pages where Chromanone synthesis is mentioned: [Pg.579]    [Pg.195]    [Pg.579]    [Pg.349]    [Pg.225]    [Pg.579]    [Pg.331]    [Pg.182]    [Pg.579]    [Pg.225]    [Pg.225]    [Pg.332]    [Pg.289]    [Pg.47]    [Pg.182]   
See also in sourсe #XX -- [ Pg.68 ]




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