Matches in SemOpenAlex for { <https://semopenalex.org/work/W2978552406> ?p ?o ?g. }
- W2978552406 endingPage "18164" @default.
- W2978552406 startingPage "18159" @default.
- W2978552406 abstract "While esters are frequently used as traditional electrophiles in substitution chemistry, their application in cross-coupling chemistry is still in its infancy. This work demonstrates that methyl esters can be used as coupling electrophiles in Ni-catalyzed Heck-type reactions through the challenging cleavage of the C(acyl)-O bond under relatively mild reaction conditions at either 80 or 100 °C. With the σ-NiII intermediate generated from the insertion of acyl NiII species into the tethered C=C bond, carbonyl-retentive products were formed by domino Heck/Suzuki-Miyaura coupling and Heck/reduction pathways when organoboron and mild hydride nucleophiles are used." @default.
- W2978552406 created "2019-10-10" @default.
- W2978552406 creator A5008582832 @default.
- W2978552406 creator A5009720118 @default.
- W2978552406 date "2019-10-28" @default.
- W2978552406 modified "2023-10-14" @default.
- W2978552406 title "Nickel‐Catalyzed Domino Heck‐Type Reactions Using Methyl Esters as Cross‐Coupling Electrophiles" @default.
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