The drimane sesquiterpenes, (+)-albicanol (2) and (+)-albicanyl acetate (3), were synthesized from an optically active bicyclic diol [(+)-1] that had been obtained via the recently developed optical resolution of a general synthetic intermediate for drimane sesquiterpenes. The crucial step in the previous syntheses was markedly improved by the modified Wittig methylenation of a silyloxy ketone (7). The high overall yield (77% in 4 or 5 steps from (+)-1) by this total synthesis makes it possible to synthesize the other biologically active drimane sesquiterpenes.
CITATION STYLE
Toshima, H., Oikawa, H., Toyomasu, T., & Sassa, T. (2001). Total Synthesis of (+)-Albicanol and (+)-Albicanyl Acetate. Bioscience, Biotechnology and Biochemistry, 65(5), 1244–1247. https://doi.org/10.1271/bbb.65.1244
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