Catalytic Enantioselective Oxidative Homocoupling of 2‐Acyl Imidazoles
نویسندگان
چکیده
A diastereoselective and enantioselective construction of 2,3-disubstituted 1,4-dicarbonyl compounds is reported. Nishiyama's RuPhebox complex (2.0 mol% catalyst loading) serves as a chiral Lewis acid in conjunction with BrCCl3 base for the oxidative homocoupling 2-acyl imidazoles via stereocontrolled reaction intermediate Ru enolates situ brominated imidazoles. Cleavage achiral imidazole auxiliary provides optically active succinic acids which are useful intermediates synthesis like natural product class lignans.
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ژورنال
عنوان ژورنال: Advanced Synthesis & Catalysis
سال: 2021
ISSN: ['1615-4169', '1615-4150']
DOI: https://doi.org/10.1002/adsc.202100837