Photocalatytic C–H Alkylation Enabled by a Zwitterionic Acridinium Amidate Catalyst

workers disclose a photocatalytic alkylation of unactivated C-H bonds using electrophilic olefins.To this end, a zwitterionic acridinium amidate was designed as a direct hydrogen atom transfer catalyst, furnishing the products in good to excellent yields.Comment: Mechanistic studies show that hydrogen bonding of the catalyst to HFIP as well as the perpendicular orientation of the 2p orbitals of the acridinium and amidate N-atoms enable the formation of a twisted, catalytically active diradical upon photoexication and intramolecular charge transfer.

Publication Details

Journal
Synfacts
Published
2024-08-16
DOI
https://doi.org/10.1055/s-0043-1775273
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00
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article

Photocalatytic C–H Alkylation Enabled by a Zwitterionic Acridinium Amidate Catalyst

Synfacts
Catalytic C–H Functionalization Methods
article

Photocalatytic C–H Alkylation Enabled by a Zwitterionic Acridinium Amidate Catalyst

article en

Abstract

workers disclose a photocatalytic alkylation of unactivated C-H bonds using electrophilic olefins.To this end, a zwitterionic acridinium amidate was designed as a direct hydrogen atom transfer catalyst, furnishing the products in good to excellent yields.Comment: Mechanistic studies show that hydrogen bonding of the catalyst to HFIP as well as the perpendicular orientation of the 2p orbitals of the acridinium and amidate N-atoms enable the formation of a twisted, catalytically active diradical upon photoexication and intramolecular charge transfer.

SynfactsVol. 20(09)
Openalex Percentile: Top 90%
Catalytic C–H Functionalization Methods
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Photocalatytic C–H Alkylation Enabled by a Zwitterionic Acridinium Amidate Catalyst · Synfacts (2024) | TGRS Research Map | TGRS