Abstract
When tri-n-butylphosphine
is used to reduce the disulphide groups in wool keratin, several different
methods can be used for the subsequent alkylation of the thiol groups formed. A
novel feature is that in some oases reduction and alkylation can be effected
using tri-n- butylphosphine and the alkylating agent acting simultaneously.
S-Alkyl kerateines have been prepared
using 11 alkylating agents of various chemical types. By means of such a
technique a quantitative and apparently specific conversion of cystinyl
residues in wool keratin to S.(2-aminoethyl)cysteinyl residues has been
achieved.
Cited by
76 articles.
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