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- W2016037164 abstract "Abstract The title compound 1, a highly strained (E)-cycloalkene, was prepared in enantiomerically pure form from the corresponding trans-1,2-diol 4 via the thionocarbonate 5. The racemic 4 was separated by enantioselective HPLC on an amylose tris(3,5-dimethylphenylcarbamate) column. The absolute configuration of 1 was determined by circular dichroism spectroscopy in connection with theoretical calculations; the (+)-enantiomer has the (S)- and the (−)-enantiomer the (R)-configuration." @default.
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- W2016037164 date "1999-09-01" @default.
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- W2016037164 title "Synthesis of enantiomerically pure (E)-1,1,3,3,6,6-hexamethyl-1-sila-4-cycloheptene and its absolute configuration" @default.
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- W2016037164 doi "https://doi.org/10.1016/s0957-4166(99)00313-4" @default.
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