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- W2034992722 abstract "[reaction: see text] Ab initio calculations were performed on a cyclohexane derivative to elucidate the mechanism of the formation of the five-membered C ring in the biosynthesis of lanosterol from squalene. A conformational analysis of the side chain containing the double bond indicated that the conformer that should give rise to the cyclized C ring is not a minimum on the potential surface. Consequently, it is suggested that it is very likely that C-ring formation occurs in concert with formation of the A and B rings." @default.
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- W2034992722 date "2003-01-01" @default.
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- W2034992722 title "Formation of the C Ring in the Lanosterol Biosynthesis from Squalene" @default.
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- W2034992722 doi "https://doi.org/10.1021/ol027449c" @default.
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