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- W2064969884 abstract "The tetracyclic sesquiterpenoid (+)-cyclomyltaylan-5α-ol 1 has been synthesized starting from (S)-(+)-Hajos–Wiechert ketone analogue 10via stereoselective Claisen rearrangement followed by SmI2-promoted reductive cyclisation. Thus, the absolute configuration has been established to be 2R,3R,4R,5S,6R,7R (cyclomyltaylane numbering) as depicted in structure 1." @default.
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- W2064969884 date "2002-02-05" @default.
- W2064969884 modified "2023-10-09" @default.
- W2064969884 title "The first enantioselective total synthesis of cyclomyltaylane-5α-ol and determination of its absolute stereochemistry" @default.
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- W2064969884 doi "https://doi.org/10.1039/b111594b" @default.
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