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A Formal Synthesis of Iridoid 9-Deoxygelsemide

A Formal Synthesis of Iridoid 9-Deoxygelsemide
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摘要 A formal total synthesis of iridoid 9-deoxygelsemide has been accomplished. Our approach features the use of (S)-carvone as starting material, Favorskii rearrangement to construct the functionalized cyclopentane core, Chugeav elimination to introduce the endocyclic double bond, and the ring-opening reaction of epoxide to build the second five-membered ring. A formal total synthesis of iridoid 9-deoxygelsemide has been accomplished. Our approach features the use of (S)-carvone as starting material, Favorskii rearrangement to construct the functionalized cyclopentane core, Chugeav elimination to introduce the endocyclic double bond, and the ring-opening reaction of epoxide to build the second five-membered ring.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2013年第1期18-22,共5页 中国化学(英文版)
关键词 IRIDOID 9-deoxygelsemide Favorskii rearrangement Chugeav elimination iridoid, 9-deoxygelsemide, Favorskii rearrangement, Chugeav elimination
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