SYNTHESIS OF C-TERMINAL PEPTIDE FRAGMENTS OF THE HEAVY CHAIN OF HEMAGGLUTININ OF INFLUENZA VIRUS OF SUBTYPES H1 AND H3

Article abstract of DOI:10.1007/BF00633395

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 10-1