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- W1990482023 abstract "Introduction of a benzenesulfonylmethyl group at the unactivated γ-carbon of carboxylic acid derivatives has been achieved through a combination of rhodium acetate catalysed carbenoid CH insertion and baker's yeast mediated kinetic resolution. Access to the two complementary enantiomeric series of 6 with excellent enantiocontrol is possible." @default.
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- W1990482023 date "1997-10-01" @default.
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- W1990482023 title "Enantioselective introduction of a benzenesulfonylmethyl substituent at an unactivated carbon atom via chemoenzymatic methods" @default.
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- W1990482023 doi "https://doi.org/10.1016/s0040-4039(97)01756-5" @default.
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