Matches in SemOpenAlex for { <https://semopenalex.org/work/W4297239541> ?p ?o ?g. }
- W4297239541 abstract "A nickel-catalyzed reductive cross-electrophile coupling between the redox-active N-trifluoroethoxyphthalimide and iodoarenes is documented. The protocol reproduces a formal arylation of trifluoroacetaldehyde under mild conditions in high yields (up to 88 %) and with large functional group tolerance (30 examples). A combined computational and experimental investigation revealed a pivotal solvent assisted 1,2-Hydrogen Atom Transfer (HAT) process to generate a nucleophilic α-hydroxy-α-trifluoromethyl C-centered radical for the Csp2 -Csp3 bond forming process." @default.
- W4297239541 created "2022-09-28" @default.
- W4297239541 creator A5027207716 @default.
- W4297239541 creator A5052232106 @default.
- W4297239541 creator A5056275487 @default.
- W4297239541 creator A5058546077 @default.
- W4297239541 creator A5059606474 @default.
- W4297239541 creator A5066849639 @default.
- W4297239541 creator A5077034819 @default.
- W4297239541 date "2022-10-18" @default.
- W4297239541 modified "2023-10-10" @default.
- W4297239541 title "Direct Synthesis of α‐Aryl‐α‐Trifluoromethyl Alcohols via Nickel Catalyzed Cross‐Electrophile Coupling" @default.
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