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- W2950705336 abstract "In the presence of iron(II) chloride (FeCl2 ; 20 mol%) and potassium tert-butoxide (t- BuOK; 4 equiv.) in dimethyl sulfoxide (DMSO), aryl and heteroaryl iodides undergo stereoselective Mizoroki–Heck C—C cross-coupling reactions with styrenes at 60 8C giving the corresponding (E)-alkenes. The best yields are obtained upon adding a ligand (80 mol%) such as proline or picolinic acid. Aryl bromides and pyridinyl bromides are also coupled with styrenes but in lower yields." @default.
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- W2950705336 date "2009-05-12" @default.
- W2950705336 modified "2023-10-01" @default.
- W2950705336 title "ChemInform Abstract: Iron-Catalyzed Mizoroki-Heck Cross-Coupling Reaction with Styrenes." @default.
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- W2950705336 doi "https://doi.org/10.1002/chin.200919089" @default.
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