Diels-Alder Reactions of 12-Hydroxy-9(10®20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
作者： George Majetich , Yong Zhang , Xinrong Tian , Ge Zou , Yang Li
DOI: 10.3390/MOLECULES18066969
关键词:
摘要: 12-Hydroxy-9(10®20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione (quinone 2) served as the dienophile in numerous intermolecular Diels-Alder reactions. These cycloadditions were conducted either thermally (including microwave heating) or with Lewis acid activation. While most dienes reacted quinone 2 good chemical yield, others incompatible under experimental conditions used.
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