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Construction of All-Carbon Quaternary Stereocenters by Scandium-Catalyzed Intramolecular C–H Alkylation of Imidazoles with 1,1-Disubstituted Alkenes

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NIAID Data Ecosystem2026-03-11 收录
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https://figshare.com/articles/dataset/Construction_of_All-Carbon_Quaternary_Stereocenters_by_Scandium-Catalyzed_Intramolecular_C_H_Alkylation_of_Imidazoles_with_1_1-Disubstituted_Alkenes/11559177
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The exo-selective C–H cycloaddition of imidazoles to 1,1-disubstituted alkenes has been achieved for the first time by using half-sandwich scandium catalysts. A wide range of imidazole compounds bearing various 1,1-disubstituted aliphatic alkenes, styrenes, dienes, and enynes have been selectively converted in high yields to the corresponding bicyclic imidazole derivatives bearing β-all-carbon-substituted quaternary stereocenters. By using a chiral half-sandwich scandium catalyst, the asymmetric exo-selective cyclization has also been achieved with a high level of enantioselectivity.
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2020-01-06
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