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DOI: 10.1039/A800727F (Paper) Reference Section for: Chem. Commun., 1998, 761-762

Total synthesis of (+)-furanomycin

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Sung Ho Kang and Sung Bae Lee

Abstract

A highly enantioselective total synthesis of (+)-furanomycin 24 has been achieved via the mercury cation-mediated cyclizations of γ-hydroxy alkene 4 and homoallylic trichloroacetimidate 11 to install the trans-2,5-disubstituted tetrahydrofuran and the (αS)-amino acid side chain, respectively.

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