Abstract
It is proposed to use the chromogenic 2-[4-phenylazo)benzylsulfonyl]ethyl group, which can be eliminated by organic bases in aprotic solvents, for the protection of a C-terminal carboxy group in the synthesis of peptides. The synthesis of a number of 10–16-membered peptides corresponding to C-terminal fragments of the heavy chain of the hemagglutination of influenza virus of subtypes H1 and H3 has been performed with the use of this group.
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