A protocol for photoinduced cross-coupling of aryl iodides having polar π-functional groups or elongated π-conjugation with alkenes has been developed. The radical cascade mechanism involving generation of aryl radicals via C-I bond homolysis of photoexcited aryl iodides and their subsequent addition to alkenes is proposed. The method enables iodide-selective cross-coupling over other halogen leaving groups with functional group compatibility on both arene and alkene motifs.Ministry of Education (MOE)Nanyang Technological UniversityAccepted versionThis work was supported by funding from Nanyang Technological University (NTU) and the Singapore Ministry of Education (Academic Research Fund Tier 2: MOE2017-T2-1-064) (for S.C.)
The routine application of Csp3-hybridized nucleophiles in cross-coupling has been an ongoing pursui...
Inter- and intramolecular additions of aryl radicals derived from aryl iodides to arenes are promote...
A simple and efficient cross-coupling of aryl halides with different alkyl disulfides under mild con...
Here we report a facile, efficient, and catalyst-free method to realize C-C cross-coupling of aryl c...
Alkyl radicals are powerful intermediates for the generation of carbon-carbon bonds, which play a...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
From PubMed via Jisc Publications RouterHistory: received 2021-06-07, accepted 2021-07-06Publication...
The photoinduced reactions of o-iodoanilides (o-IC6H 4N(Me)COR, 4a-d) with sulfur nucleophiles such ...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for th...
An unprecedented method that makes use of the cooperative interplay between molecular iodine and pho...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
We have developed a photochemical ATRA/ATRC reaction that is mediated by halogen bonding interaction...
The formation of Csp3-Csp3 bonds is arguably the most critical transformation in organic synthesis. ...
The routine application of Csp3-hybridized nucleophiles in cross-coupling has been an ongoing pursui...
Inter- and intramolecular additions of aryl radicals derived from aryl iodides to arenes are promote...
A simple and efficient cross-coupling of aryl halides with different alkyl disulfides under mild con...
Here we report a facile, efficient, and catalyst-free method to realize C-C cross-coupling of aryl c...
Alkyl radicals are powerful intermediates for the generation of carbon-carbon bonds, which play a...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
From PubMed via Jisc Publications RouterHistory: received 2021-06-07, accepted 2021-07-06Publication...
The photoinduced reactions of o-iodoanilides (o-IC6H 4N(Me)COR, 4a-d) with sulfur nucleophiles such ...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for th...
An unprecedented method that makes use of the cooperative interplay between molecular iodine and pho...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
We have developed a photochemical ATRA/ATRC reaction that is mediated by halogen bonding interaction...
The formation of Csp3-Csp3 bonds is arguably the most critical transformation in organic synthesis. ...
The routine application of Csp3-hybridized nucleophiles in cross-coupling has been an ongoing pursui...
Inter- and intramolecular additions of aryl radicals derived from aryl iodides to arenes are promote...
A simple and efficient cross-coupling of aryl halides with different alkyl disulfides under mild con...