A general, sustainable dearomatization reaction for nitrogen-containing heterocycles was developed. Under solvent free conditions and without catalyst, the biorenewable methyl coumalate (MC) reacted as an efficient C partner to convert nine types of basic aromatic rings into their pyrido[1,2-a] fused derivatives in good to excellent yields. The fluorescence properties of some of the products were harnessed to conjugate fluorescent tags to bovine serum albumin (BSA) and immunoglobulin G.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cssc.202100301DOI Listing

Publication Analysis

Top Keywords

solvent-free catalyst-free
4
catalyst-free formal
4
formal [3+3]
4
[3+3] cycloaddition
4
cycloaddition dearomatization
4
dearomatization strategy
4
strategy fluorophores
4
fluorophores biomolecules
4
biomolecules labelling
4
labelling general
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!