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Process for the Preparation of Chromones, Isoflavones and Homoisoflavones Using Vilsmeier Reagent Generated from Phthaloyl Dichloride and DMF

Process for the Preparation of Chromones, Isoflavones and Homoisoflavones Using Vilsmeier Reagent Generated from Phthaloyl Dichloride and DMF
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摘要 Vilsmeier reagent formed from phthaloyl dichloride and DMF was found to be very effective for converting 2-hydroxyacetophenones, deoxybenzoins and dihydrochalcones into corresponding chromones, isoflavones and homoisoflavones with excellent yield. This method offers significant advantages such as efficiency and mild reaction conditions with shorter reaction time. Vilsmeier reagent formed from phthaloyl dichloride and DMF was found to be very effective for converting 2-hydroxyacetophenones, deoxybenzoins and dihydrochalcones into corresponding chromones, isoflavones and homoisoflavones with excellent yield. This method offers significant advantages such as efficiency and mild reaction conditions with shorter reaction time.
出处 《International Journal of Organic Chemistry》 2014年第4期236-246,共11页 有机化学国际期刊(英文)
关键词 Phthaloyl DICHLORIDE DIMETHYLFORMAMIDE CHROMONES ISOFLAVONES Homoisoflavones BF3·Et2O Vilsmeier REAGENT Phthaloyl Dichloride Dimethylformamide Chromones Isoflavones Homoisoflavones BF3·Et2O Vilsmeier Reagent
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