The cleavage of sulfidic C-S bonds under visible-light irradiation was harnessed to generate carbocations under neutral conditions and synthesize valuable di- and triarylalkanes as well as benzyl amines. To this end, photoredox catalysis and direct photoinduced C-S bond cleavage are used as complementary approaches and participate in the versatility of the general strategy. Extensive mechanistic studies have demonstrated the diversity of the reaction mechanism at work in these different reactions
We report a redox‐neutral method for the generation of carbanions from benzylic C–H bonds in a photo...
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopro...
© 2021 Tyra Hayley HorngrenThe three-dimensional structure of proteins and receptor binding sites re...
The cleavage of sulfidic C–S bonds under visible-light irradiation was harnessed to generate carboca...
This review summarizes recent developments in photocatalyzed carbon–sulfur bond formation. General c...
A photocatalytic method for the aerobic oxidative cleavage of C=C bonds has been developed. Electron...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxy...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
Over the last decade, visible-light photoredox catalysis is rising as an important route for new che...
ABSTRACT: The photoredox-mediated coupling of benzylic ethers with Schiff bases has been accomplishe...
Aim of this thesis is the use of photo-redox catalysis for the activation of Ar-X bonds, and develop...
Carbon-carbon and carbon-hydrogen bonds constitute essential components of organic frameworks and im...
A photoactivated neutral organic super electron donor cleaves challenging arenesulfonamides derived ...
We report a redox‐neutral method for the generation of carbanions from benzylic C–H bonds in a photo...
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopro...
© 2021 Tyra Hayley HorngrenThe three-dimensional structure of proteins and receptor binding sites re...
The cleavage of sulfidic C–S bonds under visible-light irradiation was harnessed to generate carboca...
This review summarizes recent developments in photocatalyzed carbon–sulfur bond formation. General c...
A photocatalytic method for the aerobic oxidative cleavage of C=C bonds has been developed. Electron...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxy...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
Over the last decade, visible-light photoredox catalysis is rising as an important route for new che...
ABSTRACT: The photoredox-mediated coupling of benzylic ethers with Schiff bases has been accomplishe...
Aim of this thesis is the use of photo-redox catalysis for the activation of Ar-X bonds, and develop...
Carbon-carbon and carbon-hydrogen bonds constitute essential components of organic frameworks and im...
A photoactivated neutral organic super electron donor cleaves challenging arenesulfonamides derived ...
We report a redox‐neutral method for the generation of carbanions from benzylic C–H bonds in a photo...
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopro...
© 2021 Tyra Hayley HorngrenThe three-dimensional structure of proteins and receptor binding sites re...