Trifluoroacetic Acid Mediated Additive-Free Late-Stage Native Peptide Cyclization to Form Disulfide Mimetics via Thioketalization with Ketones-Reference-Cited by-同舟云学术

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Trifluoroacetic Acid Mediated Additive-Free Late-Stage Native Peptide Cyclization to Form Disulfide Mimetics via Thioketalization with Ketones

Published:2024-07-24 Issue:30 Volume:26 Page:6512-6517
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xiao Yisa¹,Zhou Haiyan¹²,Liu Han¹,Li Xuechen¹^ORCID

Affiliation:

1. Department of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, People’s Republic of China

2. Chemistry and Chemical Engineering Guangdong Laboratory, Shantou, Guangdong Province 515063, People’s Republic of China

Funder

Research Grants Council, University Grants Committee

Innovation and Technology Commission

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02464

Reference29 articles.

1. Cyclic peptide drugs approved in the last two decades (2001–2021)

2. Peptide stapling techniques based on different macrocyclisation chemistries

3. Peptide macrocyclization by transition metal catalysis

4. Multifaceted Roles of Disulfide Bonds. Peptides as Therapeutics

5. Converting disulfide bridges in native peptides to stable methylene thioacetals

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