@article{208de99bcb284bc5ad9f297c522c1bc5,
title = "Fluorogenic Protein Labeling by Generation of Fluorescent Quinoliziniums Using [Cp*RhCl2]2",
abstract = "Fluorogenic labeling has received considerable attention as a result of the high demand in chemical biology and synthetic biology applications. Herein, we develop a new strategy for fluorescent turn-on ligation targeting alkyne- and quinoline-linked peptides and proteins (λem of 515 nm and up to φF of 0.20) using the [Cp*RhCl2]2 catalyst. The good conversion, high flexibility, broad utility, ease of use, and mild reaction conditions are great advantages to extend the rhodium-mediated turn-on fluorogenic bioconjugation for further applications.",
author = "Ajcharapan Tantipanjaporn and Kung, {Karen Ka Yan} and Wong, {Man Kin}",
note = "Funding Information: The authors gratefully acknowledge the financial support by the Shenzhen Science and Technology Innovation Commission (JCYJ20170818104257975), the Hong Kong Research Grants Council (15300117), the State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University (ZVVG), and the Innovation and Technology Commission (PRP/075/19FX). The authors acknowledge the technical support of the University Research Facility in Life Sciences (ULS) and the University Research Facility in Chemical and Environmental Analysis (UCEA) of The Hong Kong Polytechnic University. Publisher Copyright: {\textcopyright} 2022 American Chemical Society.",
year = "2022",
month = aug,
day = "12",
doi = "10.1021/acs.orglett.2c02389",
language = "English",
volume = "24",
pages = "5835--5839",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "31",
}