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Enol sulfonates halogenation

Fig. 4. Asymmetric halogenation of silyl enol ethers derived from camphor-10-sulfonic acid esters. Fig. 4. Asymmetric halogenation of silyl enol ethers derived from camphor-10-sulfonic acid esters.
TBDMS triflate also catalyzes the ene reaction of sulfur dioxide with silyl enol ethers. The silyl sulfinate intermediates can be halogenated to the corresponding sulfonyl halide, and subsequently trapped with an amine or alcohol to give sulfonamides or sulfonate esters, respectively (eq 51). ... [Pg.134]

See other pages where Enol sulfonates halogenation is mentioned: [Pg.201]    [Pg.201]    [Pg.180]    [Pg.527]    [Pg.693]    [Pg.180]    [Pg.527]    [Pg.693]    [Pg.732]    [Pg.143]    [Pg.65]    [Pg.24]    [Pg.189]    [Pg.648]    [Pg.135]    [Pg.1062]    [Pg.408]   
See also in sourсe #XX -- [ Pg.7 , Pg.121 , Pg.530 ]

See also in sourсe #XX -- [ Pg.7 , Pg.121 , Pg.530 ]



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