Deprotection of S-acetamidomethyl cysteine with copper(ii) and 1,2-aminothiols under aerobic conditions-Reference-Cited by-同舟云学术

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Deprotection of S-acetamidomethyl cysteine with copper(ii) and 1,2-aminothiols under aerobic conditions

Published:2020 Issue:42 Volume:18 Page:8638-8645
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kobayashi Daishiro¹²³⁴,Naruse Naoto¹²³⁴,Denda Masaya¹²³⁴^ORCID,Shigenaga Akira¹²³⁴^ORCID,Otaka Akira¹²³⁴^ORCID

Affiliation:

1. Insutitute of Biomedical Sciences and Graduate School of Pharmaceutical Sciences

2. Tokushima University

3. Tokushima 770-8505

4. Japan

Abstract

1,2-Aminothiols operate as an S-deprotecting reagent for an S-Acm cysteine with the aid of CuSO₄ under aerobic conditions.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01475C

Reference24 articles.

1. Acetamidomethyl. A Novel Thiol Protecting Group for Cysteine

2. Synthesis of Four-Disulfide Insulin Analogs via Sequential Disulfide Bond Formation

3. Silver trifluoromethanesulphonate as an S-deprotecting reagent for the synthesis of cystine peptides

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

5. The Synthesis of Cystine Peptides by Iodine Oxidation ofS-Trityl-cysteine andS-Acetamidomethyl-cysteine Peptides

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