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- W2069725066 abstract "All of the conventional S-protecting groups of cysteine which were tested could be selectively converted to the 3-nitro-2-pyridinesulfenyl (Npys) group after treatment with an appropriate Npys halide. Unidirectional formation of an unsymmetrical disulfide bond is possible when Cys (Npys) is mixed with a free thiol of another Cys residue. Some of these features were exploited during the solid phase synthesis of lysine8-vasopressin." @default.
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- W2069725066 date "1982-06-05" @default.
- W2069725066 modified "2023-10-16" @default.
- W2069725066 title "ACTIVATION OF CONVENTIONAL<i>S</i>-PROTECTING GROUPS OF CYSTEINE BY CONVERSION INTO THE 3-NITRO-2-PYRIDINESULFENYL (NPYS) GROUP" @default.
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- W2069725066 doi "https://doi.org/10.1246/cl.1982.921" @default.
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