Regio-and diastereoselective synthesis of cyclobutylated phenothiazines via [2+ 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live …

S Sharangi, B Chakraborty, RK Jha, S Mandal… - Chemical …, 2025 - pubs.rsc.org
Herein, we unveiled a regio-and diastereoselective synthesis of cyclobutylated
phenothiazines, a unique class of structural congeners of phenothiazines via visible-light …

A multicomponent reaction for modular assembly of indole-fused heterocycles

J Li, H Ni, W Zhang, Z Lai, H Jin, L Zeng, S Cui - Chemical Science, 2024 - pubs.rsc.org
Indoles are privileged chemical entities in natural products and drug discovery. Indole-fused
heterocycles, particularly seven-membered ones, have received increasing attention due to …

Visible-light mediated selective phosphonylation modification of tryptophan residues in oligopeptides

W Xiong, J He, J Liu, P Chen, S Xu, Y Liu… - Organic Chemistry …, 2024 - pubs.rsc.org
Despite their significant importance in biological and medicinal chemistry fields, the
difficulties in the site-selective and diverse modification of biomolecules pose substantial …

Indole Nucleophile Triggers Mechanistic Divergence in Ni‐Photoredox N–Arylation

KJ Liang, OR Taylor, AL López, RJ Woo… - … A European Journal, 2024 - Wiley Online Library
This study presents a Ni‐photoredox method for indole N‐arylation, broadening the range of
substrates to include indoles with unprotected C3‐positions and base‐sensitive groups …

Regio-Selective Arylation Reaction for the Trp-Unit of Oligopeptides

H Yamamoto, T Hattori - Synfacts, 2024 - thieme-connect.com
Exploring an efficient and general strategy of late-stage modification of structural
complicated peptides is a central issue in organic peptide chemistry. The authors have …