Novel synthesis of trans-tetrahydro diol diacetates precursors of carcinogenic aza-arene dihydro diols and diol epoxides
作者:Subodh Kumar
DOI:10.1016/s0040-4039(00)99015-4
日期:——
Selective dehydrogenation of -octahydro diol diacetates of dibenz(a,h)acridine by DDQ provides a convenient synthesis of trans-tetrahydro diol diacetates which are the valuable intermediates for the synthesis of proximate and ultimate carcinogens of dibenz(a,h)acridine.
DDQ对二
苯并(a,h)ac啶的-八
氢二醇二
乙酸酯进行选择性
脱氢提供了方便的反式四
氢二醇二
乙酸酯的合成,这是合成二
苯并(a,h)ac啶的最接近和最终致癌物的有价值的
中间体。