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2.2.2- Trichloroethyl protected phosphates

H-1,2,3-Triazoles, l-alkyl-4,5-dihydro-, 153 1/f-1,2,4-Triazoles, l-farylsulfonyl)- nucleotide condensation with, 218 2H-1,2,3-Triazoles, 2-alkyl- synth., 151-152 2 2-Tribromoethoxycarbonyl (Tbeoc) protected alcohols and amines, 157-158, 163 2,2,2-Trichloroethoxycarbonyl (Tceoc) protected alcohols and amines, 157-158,162-163 2,2 -Trichloroethyl (Tee) protected phosphates, 166-167, 216, 218... [Pg.222]

As phosphate-protecting groups, in addition to the 8 -cyanMthyl, the 8,8,8-trichloroethyl" and ethylthio ester and aromatic amidate groups m>pear to... [Pg.339]

The trichloroethyl function may be selectively removed (zinc) leaving a protected nucleoside 3 -phosphate. This can be converted to a phosphodiester by reaction with an appropriate nucleoside, in the presence of a condensing (coupling) agent ... [Pg.161]

See other pages where 2.2.2- Trichloroethyl protected phosphates is mentioned: [Pg.117]    [Pg.217]    [Pg.170]    [Pg.92]    [Pg.315]    [Pg.376]    [Pg.587]    [Pg.217]    [Pg.168]    [Pg.174]    [Pg.187]    [Pg.155]    [Pg.173]    [Pg.307]    [Pg.532]    [Pg.534]    [Pg.380]    [Pg.337]    [Pg.100]    [Pg.339]    [Pg.66]    [Pg.194]    [Pg.338]    [Pg.340]    [Pg.83]    [Pg.277]    [Pg.224]    [Pg.42]    [Pg.43]    [Pg.139]    [Pg.12]   
See also in sourсe #XX -- [ Pg.166 , Pg.216 , Pg.218 ]



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