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Triflates destabilized

They reasoned that the electron-withdrawing effect of the 0-2 sulfonyl group would destabilize the oxocarbenium ion, thereby shifting the equilibrium toward a covalent ot-mannosyl triflate, which would react with an acceptor in an SN2-like fashion to generate the p-mannoside [19]. [Pg.113]

See other pages where Triflates destabilized is mentioned: [Pg.40]    [Pg.41]    [Pg.282]    [Pg.111]    [Pg.112]    [Pg.52]    [Pg.282]    [Pg.194]    [Pg.312]    [Pg.173]    [Pg.507]    [Pg.311]    [Pg.61]    [Pg.67]    [Pg.84]    [Pg.119]    [Pg.158]    [Pg.162]    [Pg.163]    [Pg.165]    [Pg.166]    [Pg.42]    [Pg.582]    [Pg.211]    [Pg.411]   
See also in sourсe #XX -- [ Pg.96 , Pg.192 ]



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