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- W1972502406 abstract "Lewis acid -promoted triethylsilane reduction of 6,6-spiroketal alcohols produces cis-2,6-disubstituted tetrahydropyrans with excellent regioselectivity and stereocontrol. An appended alcohol allows bidentate coordination of the Lewis acid to selectively activate one CO bond of the anomeric center toward reductive cleavage." @default.
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- W1972502406 date "1996-08-01" @default.
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- W1972502406 title "Regioselective and stereoselective reductive cleavage of 1,7-dioxaspiro[5.5]undecane alcohols" @default.
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- W1972502406 doi "https://doi.org/10.1016/0040-4039(96)01196-3" @default.
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