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- W4377014591 abstract "In this issue of Chem Catalysis, Cho and co-workers invent an innovative way to easily synthesize all-carbon tetra-substituted olefins through a regio- and stereoselective hydroacylation of both 1,1-disubstituted symmetric and unsymmetrical allenes with various anhydrides. This PˆN ligand-ligated NiH system reveals a complementary regioselectivity to Cu catalysis." @default.
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- W4377014591 date "2023-05-01" @default.
- W4377014591 modified "2023-09-29" @default.
- W4377014591 title "Synthesis of tetra-substituted olefins by NiH-catalyzed hydroacylation of allenes" @default.
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- W4377014591 doi "https://doi.org/10.1016/j.checat.2023.100633" @default.
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