The Cysteine S-Alkylation Reaction as a Synthetic Method to Covalently Modify Peptide Sequences-Reference-Cited by-同舟云学术

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The Cysteine S-Alkylation Reaction as a Synthetic Method to Covalently Modify Peptide Sequences

Published:2016-08-19 Issue:2 Volume:23 Page:224-233
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Calce Enrica¹,De Luca Stefania¹

Affiliation:

1. Institute of Biostructures and Bioimaging; National Research Council; Via Mezzocannone, 16 80134 Naples Italy

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference45 articles.

1. Peptidomimetics—Tailored Enzyme Inhibitors

2. Peptidmimetica – maßgeschneiderte Enzyminhibitoren

3. Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics

4. Chemical Modification of Proteins at Cysteine: Opportunities in Chemistry and Biology

5. Protein Chemical Modification on Endogenous Amino Acids

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4. Solid-State Strategy for the S-Conjugation of Peptides Catalyzed by Zeolites and Promoted by Microwave Radiation: A Green Approach;ACS Sustainable Chemistry & Engineering;2024-01-22

5. S-Alkylation of cysteine-containing peptides using thianthenium salts as an alkyl source in flow;Green Chemistry;2024

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