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Total synthesis of the duocarmycins
Authors:Yamada Ken  Kurokawa Toshiki  Tokuyama Hidetoshi  Fukuyama Tohru
Institution:Graduate School of Pharmaceutical Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.
Abstract:The total synthesis of (+)-duocarmycin A and SA through a common indoline intermediate is described. The key reactions include selective lithiation of a 2,6-dibromoiodobenzene derivative and diastereoselective addition to a chiral nitroalkene, copper-mediated aryl amination, and addition of aryllithium to azlactones.
Keywords:
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