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Chem Pharm Bull (Tokyo) ; 60(1): 94-103, 2012.
Article in English | MEDLINE | ID: mdl-22223380

ABSTRACT

(±)-8-Deisopropyladunctin B, the deisopropyl form of adunctin B, which was isolated from the leaves of Piper aduncum (Piperaceae) collected in Papua New Guinea, was synthesized in 0.77% overall yield in 17 steps from 5,7-dimethoxycoumarin-3-carboxylate. The key step was our original stereoconvergent skeleton transformation from 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-one to 1,2,4a,9b-tetrahydrodibenzofuran-4-ol with dimethylsulfoxonium methylide.


Subject(s)
Benzofurans/chemical synthesis , Pyrans/chemistry , Benzofurans/chemistry , Dicarboxylic Acids/chemistry , Piper/chemistry , Plant Leaves/chemistry , Pyrans/chemical synthesis , Stereoisomerism , Sulfonium Compounds/chemistry
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