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A convenient route to the furopyran core of dysiherbaine
Okiko Miyata1, Ryuichi Iba, Jun Hashimoto
1Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan.
Abstract:
The bicyclic core, furo[3,2-b]pyran, of the dysiherbaines has been synthesized via two routes involving the imino 1,2-Wittig rearrangement of allyl furohydroximate and the asymmetric dihydroxylation of furylpropenol derivative.
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