| Autor: |
Kalashnikov, V. V., Samukov, V. V. |
| Zdroj: |
Chemistry of Natural Compounds; September 1988, Vol. 24 Issue: 5 p624-629, 6p |
| Abstrakt: |
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. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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