Late-Stage N-Arylation of Tryptophan-Containing Peptides and Drug Molecules via Arylthianthrenium Salts DOI
Haoxiang Zhang,

Huimin Dong,

Ye Wu

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Май 15, 2025

We report herein a mild and efficient method for the late-stage N-arylation of tryptophan tryptophan-containing peptides using readily accessible arylthianthrenium salts through dual photoredox/copper catalysis. Applying this protocol, library noncanonical amino acids N-arylated was facilely prepared. Moreover, protocol enables peptide ligation conjugation, offering convenient access to ligated peptide/drug conjugates. Remarkably, strategy can also be applied modification complex drug molecules.

Язык: Английский

Site-selective cleavage of peptides and proteins targeting aromatic amino acid residues DOI Creative Commons
A. Bandyopadhyay, Rajib Sarkar

RSC Advances, Год журнала: 2025, Номер 15(12), С. 9159 - 9179

Опубликована: Янв. 1, 2025

This review provides an account of the site-selective cleavage peptides and proteins at aromatic amino acid residues, developed over last seven decades (1958–2024).

Язык: Английский

Процитировано

2

Residue-Specific Protein-Glycan Conjugation Strategies for the Development of Pharmaceutically Promising Glycoconjugate Vaccines: A Recent Update DOI
Rajib Sarkar, A. Bandyopadhyay, Goutam Brahmachari

и другие.

Carbohydrate Research, Год журнала: 2025, Номер unknown, С. 109476 - 109476

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Late-Stage N-Arylation of Tryptophan-Containing Peptides and Drug Molecules via Arylthianthrenium Salts DOI
Haoxiang Zhang,

Huimin Dong,

Ye Wu

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Май 15, 2025

We report herein a mild and efficient method for the late-stage N-arylation of tryptophan tryptophan-containing peptides using readily accessible arylthianthrenium salts through dual photoredox/copper catalysis. Applying this protocol, library noncanonical amino acids N-arylated was facilely prepared. Moreover, protocol enables peptide ligation conjugation, offering convenient access to ligated peptide/drug conjugates. Remarkably, strategy can also be applied modification complex drug molecules.

Язык: Английский

Процитировано

0