Environment-sensitive fluorescent tryptophan analogues via indole C-2 alkenylation reactions
Year: 2025
Type: article
Abstract: A modular synthetic strategy for the preparation of intrinsically fluorescent unnatural α-amino acids by C-2 oxidation and alkenylation of a tryptophan-derived tetrahydro-β-carboline is described. This approach yielded a novel tryptophan-coumarin hybrid with strong environmental sensitivity and compatibility with near-infrared two-photon excitation.
Source: Chemical Communications
DOI: 10.1039/d5cc02114f
Authors: Valeria K. Burianova, Liyao Zeng, Abigail W. Thom, Niamh C. Radcliffe-Kennedy, Steven W. Magennis, Andrew Sutherland
Institution: University of Glasgow
Language: English
Subfield: Spectroscopy
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
OpenAlex ID: W4411673303
