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Iron-catalyzed AlkylAlkyl negishi coupling of organoaluminum reagents
- Source :
- Chemistry Letters. 48(3):238-241
- Publication Year :
- 2019
- Publisher :
- Chemical Society of Japan, 2019.
-
Abstract
- The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl–alkyl Negishi coupling) is developed using an iron/bisphosphine catalyst system. The reaction shows high functional group tolerance: various primary alkyl halides possessing a non-protected indole, carboxyl, or hydroxy group are coupled with primary alkylaluminum reagents in good yields. Potassium fluoride plays a key role to promote the reaction by generating an aluminate species, which facilitates the transmetalation between the organoaluminum and the iron catalyst.
- Subjects :
- chemistry.chemical_classification
010405 organic chemistry
Negishi coupling
Organoaluminum
Iron catalyzed
Iron
Halide
General Chemistry
010402 general chemistry
01 natural sciences
0104 chemical sciences
Catalysis
chemistry
Reagent
Polymer chemistry
Cross-coupling
lipids (amino acids, peptides, and proteins)
Alkyl
Subjects
Details
- Language :
- English
- ISSN :
- 03667022
- Volume :
- 48
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Chemistry Letters
- Accession number :
- edsair.doi.dedup.....fb75af83e2da88c4ca976c298aa04e2c