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The second step is removal of the DMT protecting group by treatment with dichloroacetic acid in CH2C12- The reaction occurs by an S14I mechanism and proceeds rapidly because of the stability of the tertiary, henzylic dimethoxy-trityl cation. [Pg.1002]

See other pages where Trityl cations dimethoxy is mentioned: [Pg.553] [Pg.553] [Pg.553] [Pg.354]

See also in sourсe #XX -- [ Pg.300 ]

See also in sourсe #XX -- [ Pg.300 ]

See also in sourсe #XX -- [ Pg.98 , Pg.300 ]