Electrochemical late-stage functionalization
Late-stage functionalization (LSF) constitutes a powerful strategy for the assembly or
diversification of novel molecular entities with improved physicochemical or biological …
diversification of novel molecular entities with improved physicochemical or biological …
Electrochemistry for the chemoselective modification of peptides and proteins
Although electrochemical strategies for small-molecule synthesis are flourishing, this
technology has yet to be fully exploited for the mild and chemoselective modification of …
technology has yet to be fully exploited for the mild and chemoselective modification of …
Tandem Electrochemical Oxidative Azidation/Heterocyclization of Tryptophan‐Containing Peptides under Buffer Conditions
Y Weng, X Xu, H Chen, Y Zhang… - Angewandte Chemie, 2022 - Wiley Online Library
As the aromatic tryptophan (Trp) side chain plays a pivotal role in influencing the structure
and function of peptides and proteins, it has become an attractive target for the late‐stage …
and function of peptides and proteins, it has become an attractive target for the late‐stage …
Tunable Electrochemical Peptide Modifications: Unlocking New Levels of Orthogonality for Side‐Chain Functionalization
D Karipal Padinjare Veedu, LA Connal… - Angewandte Chemie …, 2023 - Wiley Online Library
Electrochemical transformations provide enticing opportunities for programmable, residue‐
specific peptide modifications. Herein, we harness the potential of amidic side‐chains as …
specific peptide modifications. Herein, we harness the potential of amidic side‐chains as …
Recent progress in electrochemical modification of amino acids and peptides
F Xinyue, H Yawen, H Xinwei… - Chinese Journal of Organic …, 2024 - sioc-journal.cn
With the increasing importance of peptides in the treatment of oncological diseases and
biomedical applications, the development and construction of new methods for peptide …
biomedical applications, the development and construction of new methods for peptide …
Electrochemical modification of polypeptides at selenocysteine
AS Mackay, JWC Maxwell, MJ Bedding… - Angewandte …, 2023 - Wiley Online Library
Mild strategies for the selective modification of peptides and proteins are in demand for
applications in therapeutic peptide and protein discovery, and in the study of fundamental …
applications in therapeutic peptide and protein discovery, and in the study of fundamental …
Electrochemical regioselective cross-dehydrogenative coupling of indoles with xanthenes
X Chen, H Liu, H Gao, P Li, T Miao… - The Journal of Organic …, 2021 - ACS Publications
An electrochemical cross-dehydrogenative coupling of indoles with xanthenes has been
established at room temperature. This coupling reaction could proceed in the absence of …
established at room temperature. This coupling reaction could proceed in the absence of …
Electrochemical Nickel‐Catalyzed Selective Inter‐and Intramolecular Arylations of Cysteine‐Containing Peptides
L Shen, O Monasson, E Peroni… - Angewandte Chemie …, 2023 - Wiley Online Library
Here we report a simple electrochemical route towards the synthesis of S‐arylated peptides
by a site selective coupling of peptides with aryl halides under base free conditions. This …
by a site selective coupling of peptides with aryl halides under base free conditions. This …
Electrochemical formal [3+ 2] cycloaddition of azobenzenes with hexahydro-1, 3, 5-triazines
C Li, Q Zhong, S Tang, L Wang, P Li… - Organic Chemistry …, 2022 - pubs.rsc.org
A catalyst-free electrochemical [3+ 2] cycloaddition of azobenzenes with hexahydro-1, 3, 5-
triazines in the absence of any external oxidant is developed for constructing the 1, 2, 4 …
triazines in the absence of any external oxidant is developed for constructing the 1, 2, 4 …
Electrochemical chemoselective hydroxyl group transformation: anthranilic acyl modification of tyrosine bioconjugations
S You, R Wang, C Ma, C Lu, G Yang, L Liu… - Organic Chemistry …, 2023 - pubs.rsc.org
Herein, we report an electrochemically promoted chemoselective hydroxyl group
transformation for accessing tyrosine-containing biomolecules with valuable anthranilic acid …
transformation for accessing tyrosine-containing biomolecules with valuable anthranilic acid …