April 24, 2024

Engaging Alkenes in Metallaphotoredox: A Triple Catalytic, Radical Sorting Approach to Olefin-Alcohol Cross-Coupling

Puntos clave

Los puntos clave no están disponibles para este artículo en este momento.

Resumen

Metallaphotoredox cross-coupling is a well-established strategy for generating clinically privileged aliphatic scaffolds via single-electron reactivity. Correspondingly, expanding metallaphotoredox to encompass new C(

Me gusta

Guardar

Cite This Study

Cai et al. (Wed,) studied this question.

synapsesocial.com/papers/68e6dc0eb6db643587657d7e https://doi.org/https://doi.org/10.1021/jacs.4c02316

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Free-radical substitution reactions : bimolecular homolytic substitutions (Sh2 reactions) at saturated multivalent atoms1971 · 29 citations
2Diastereoselective Cobalt-Catalyzed Aldol and Michael Cycloreductions2001 · 119 citations
3Nickel-Catalyzed Reductive Coupling of Alkynes and Epoxides2003 · 143 citations
4Natural-Products-Inspired Use of the <i>gem</i> -Dimethyl Group in Medicinal Chemistry2017 · 137 citations
5The Persistent Radical Effect: A Principle for Selective Radical Reactions and Living Radical Polymerizations2001 · 1,316 citations

Me gusta

Guardar