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Additions triisopropylsilyl trifluoromethanesulfonate

Conjugate Addition of Alkynylzinc Bromides. Alky nylzinc bromides undergo conjugate addition with a,p-unsaturated ketones in the presence of TBDMS triflate in ether-THF at —40°C to give the corresponding 1,4-adducts (54-96% yields). A representative example is illustrated in eq 7. Other trialkylsilyl triflates such as Triisopropylsilyl Trifluoromethanesulfonate or... [Pg.90]

Trifluoromethanesulfonic acid (0.226 mol) is added dropwise to triisopropylsilane (0.242 mol), stirred under an inert atmosphere and cooled to 0 °C in a flask fitted with dropping funnel, gas inlet, exit tubes and thermometer. After the addition is completed, stirring is continued at 22 °C for 16 h. Triisopropylsilyl triflate (97%) is isolated by the distillation through a 30 cm vacuum jacketed Vigreux column. [Pg.407]


See other pages where Additions triisopropylsilyl trifluoromethanesulfonate is mentioned: [Pg.201]    [Pg.231]    [Pg.216]    [Pg.128]   
See also in sourсe #XX -- [ Pg.634 ]




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Triisopropylsilyl

Triisopropylsilyl trifluoromethanesulfonate

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