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Diversity‐Oriented Synthesis of Furo[3,2‐c]coumarins and Benzofuranyl Chromenones through Chemoselective Acylation/Wittig Reaction
Authors:Chun‐Kai Lin  Dr. Praneeth Karanam  Dr. Ganapuram Madhusudhan Reddy  Dr. Yi‐Ling Tsai  Prof. Dr. Wenwei Lin
Affiliation:Department of Chemistry, National Taiwan Normal University, Taipei, Taiwan, R.O.C.
Abstract:A highly efficient and chemoselective one‐pot protocol for the diversity‐oriented synthesis of two types of coumarin‐based formal cross‐coupling adducts, furo[3,2‐c]coumarins and 3‐benzofuranyl chromenones, is described. Key attributes of the methodology are an initial chemoselective acylation of functionalized phosphorus zwitterions and a subsequent chemoselective intramolecular Wittig reaction that preferentially resulted in one of the two coumarin derivatives in high yield, depending on relative reactivities and the addition sequence of the acylating agents.
Keywords:chemoselectivity  diversity-oriented synthesis  multicomponent reactions  organophosphonium salts  Wittig reactions
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