Palladium and visible-light mediated carbonylative Suzuki–Miyaura coupling of unactivated alkyl halides and aryl boronic acids

Author:

Roslin Sara12345ORCID,Odell Luke R.12345ORCID

Affiliation:

1. Organic Pharmaceutical Chemistry

2. Department of Medicinal Chemistry

3. Uppsala Biomedical Center

4. Uppsala University

5. Uppsala

Abstract

An efficient carbonylative coupling of aryl boronic acids and unactivated alkyl halides under visible-light irradiation and low CO-pressure is presented.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Reference49 articles.

1. H. M. Colquhoun , D. J.Thompson and M. W.Twigg, Carbonylation – Direct synthesis of carbonyl compounds, Springer Science + Business Media, New York, 1991, pp. 1–281

2. Palladium-Catalyzed Carbonylation Reactions of Aryl Halides and Related Compounds

3. Palladium-catalyzed carbonylative coupling reactions between Ar–X and carbon nucleophiles

4. Applied Cross-Coupling Reactions, ed. Y. Nishihara, Springer, Berlin, Heidelberg, 2013, pp. 1–247

5. DFT Study of Small Palladium Clusters Pd n and Their Interaction with a CO Ligand ( n = 1–9)

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