Reaction of 2-(trifluoromethyl)chromones with pyridoxal: Formation of 1-benzopyranooxepino- and 1-benzopyranopyranopyridines
作者:Vyacheslav Ya Sosnovskikh、Vladislav Yu Korotaev、Alexey Yu Barkov、Anna A. Sokovnina、Mikhail I. Kodess
DOI:10.1016/j.jfluchem.2012.06.001
日期:2012.9
Pyridoxal undergoes oxa-Michael initiated ring closure with 2-(trifluoromethyl)chromones giving 11a,13-dihydro-6H-1-benzopyrano[3′,2′:6,7]oxepino[3,4-c]pyridin-6-ones and 6H,11aH-1-benzopyrano[3′,2′:5,6]pyrano[2,3-c]pyridin-6-ones. Participation of alcoholic hydroxy group of pyridoxal in the initial oxa-Michael addition leads to the former product and that of the phenyl hydroxy group to the later one
吡rid醛与2-(三氟甲基)色酮进行oxa-Michael引发的闭环反应,生成11a,13-dihydro-6 H -1-苯并吡喃并[3',2':6,7]氧庚啶[3,4- c ]吡啶6 -ones和6 H,11a H -1-benzopyrano [3',2':5,6] pyrano [2,3- c ] pyridin-6-ones。吡ido醛的醇羟基参与初始的oxa-Michael加成反应生成了前一种产物,而苯基羟基的羟基参与了后者生成的产物。