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- W2144368221 abstract "2,3 -epoxy alcohols-1-tosylates are regio and chemoselectively opened to the corresponding 3-halohydrins (I, Br, Cl): the reduction of the iodohydrins to the monoprotected diols and subsequent standard coupling of the tosyl group leads to a straightforward synthesis of optically active naturally occurring pheromones." @default.
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- W2144368221 date "1994-01-01" @default.
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- W2144368221 title "Ring opening of 2,3-epoxy 1-tosylates to halohydrins and subsequent elaboration to asymmetrical alcohols" @default.
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- W2144368221 doi "https://doi.org/10.1016/s0040-4039(00)75820-5" @default.
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