The synthesis of a 3‐arylisoquinoline alkaloid, decumbenine B, was accomplished in a reaction sequence based on the formation of an indolizine ring {dibenz[a,f]indolizin‐5(7H)‐one} followed by its cleavage at the amide bond, starting with an interaction of 5,6‐(methylenedioxy)isoquinoline with 2‐bromo‐5,6‐(methylenedioxy)benzoyl chloride in the presence of Bu3SnH.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
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Wada et al. (2007) studied this question.
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