Disulfide bond formation in S-Acetamidomethyl cysteine-containing peptides by the combination of silver trifluoromethanesulfonate and dimethylsulfoxide / aqueous HCl-Reference-Cited by-同舟云学术

Disulfide bond formation in S-Acetamidomethyl cysteine-containing peptides by the combination of silver trifluoromethanesulfonate and dimethylsulfoxide / aqueous HCl

Published:1993-07 Issue:31 Volume:34 Page:4931-4934
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tamamura Hirokazu,Otaka Akira,Nakamura Junko,Okubo Kaori,Koide Takaki,Ikeda Kyoko,Fujii Nobutaka

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. New procedure for the synthesis of cystine-peptides by oxidation of S-substituted cysteine-peptides with thallium(III) trifluoroacetate

2. Studies on peptides. CLI. Syntheses of cystine-peptides by oxidation of s-protected cysteine-peptides with thallium(III) trifluoroacetate.

3. Sulphoxide-directed disulphide bond-forming reaction for the synthesis of cystine peptides

4. Studies on peptides CLVIII. Model experiments for the synthesis of open-chain unsymmetrical cystine-peptides

5. Application of dimethylsulphoxide(DMSO) / trifluoroacetic acid(TFA) oxidation to the synthesis of cystine-containing peptide

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