Ryan Dykstra
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View article: CCDC 2172148: Experimental Crystal Structure Determination
CCDC 2172148: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2086919: Experimental Crystal Structure Determination
CCDC 2086919: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2172149: Experimental Crystal Structure Determination
CCDC 2172149: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2086920: Experimental Crystal Structure Determination
CCDC 2086920: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2145549: Experimental Crystal Structure Determination
CCDC 2145549: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 2052602: Experimental Crystal Structure Determination
CCDC 2052602: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: Catalyst‐Free Decarbonylative Trifluoromethylthiolation Enabled by Electron Donor‐Acceptor Complex Photoactivation
Catalyst‐Free Decarbonylative Trifluoromethylthiolation Enabled by Electron Donor‐Acceptor Complex Photoactivation Open
A catalyst‐ and additive‐free decarbonylative trifluoromethylthiolation of aldehyde feedstocks has been developed. This operationally simple, scalable, and open‐to‐air transformation is driven by the selective photoexcitation of electron d…
View article: Photocatalyzed Diastereoselective Isomerization of Cinnamyl Chlorides to Cyclopropanes
Photocatalyzed Diastereoselective Isomerization of Cinnamyl Chlorides to Cyclopropanes Open
Endergonic isomerizations are thermodynamically unfavored processes that are difficult to realize under thermal conditions. We report a photocatalytic and diastereoselective isomerization of acyclic cinnamyl chlorides to strained cycloprop…
View article: Photocatalyzed DiastereoselectiveIsomerization ofCinnamyl Chlorides to Cyclopropanes
Photocatalyzed DiastereoselectiveIsomerization ofCinnamyl Chlorides to Cyclopropanes Open
Endergonic
isomerizations are thermodynamically unfavored processes
that are difficult to realize under thermal conditions. We report
a photocatalytic and diastereoselective isomerization of acyclic cinnamyl
chlorides to strained cycloprop…
View article: Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis Open
Herein, the introduction of oxa- and azabenzonorbornadienes into photoredox/nickel dual catalysis in a regioselective and diastereoselective transformation is disclosed. The inherent advantages of this dual catalytic system allow the use o…
View article: Engaging sulfinate salts <i>via</i> Ni/photoredox dual catalysis enables facile C<sub>sp2</sub>–SO<sub>2</sub>R coupling
Engaging sulfinate salts <i>via</i> Ni/photoredox dual catalysis enables facile C<sub>sp2</sub>–SO<sub>2</sub>R coupling Open
A new, mild, functional-group tolerant approach to the construction aryl- and heteroaryl sulfones via Ni/photoredox dual catalysis is described.