Ethynylbenziodoxolones (EBXs) are commonly used as radical traps in photocatalytic alkynylations. Herein, we report that aryl-substituted EBX reagents can be directly activated by visible light irradiation. They act as both oxidants and radical traps, alleviating the need for a photocatalyst in several reported EBX-mediated processes, including decarboxylative and deboronative alkynylations, the oxyalkynylation of enamides and the C-H alkynylation of THF. Furthermore, the method could be applied to the synthesis of alkynylated quaternary centers from tertiary alcohols via stable oxalate salts and from tertiary amines via aryl imines. A photocatalytic process using 4CzIPN as an organic dye was also developed for the deoxyalkynylation of oxalates.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596672PMC
http://dx.doi.org/10.1002/anie.202110257DOI Listing

Publication Analysis

Top Keywords

radical traps
8
direct photoexcitation
4
photoexcitation ethynylbenziodoxolones
4
ethynylbenziodoxolones alternative
4
alternative photocatalysis
4
photocatalysis alkynylation
4
alkynylation reactions*
4
reactions* ethynylbenziodoxolones
4
ethynylbenziodoxolones ebxs
4
ebxs commonly
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!