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• W2049206896 abstract "In hexane, i.e. under heterogeneous conditions, 1,(ω-1)-dienes readily undergo double deprotonation to give bis(allylmetal) intermediates. In tetrahydrofuran at − 75 or − 50°C, however, only mono-metalation occurs with dienes having chains of up to 12 carbon atoms. The practical potential of such selective monosubstitution reactions is demonstrated by two novel pheromone syntheses." @default.
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• W2049206896 date "1991-05-01" @default.
• W2049206896 modified "2023-09-26" @default.
• W2049206896 title "1,(ω - 1)-Dienes: solvent controlled unilateral or bilateral metalation" @default.
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• W2049206896 doi "https://doi.org/10.1016/0022-328x(91)86133-b" @default.
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