Synthesis of (Poly)fluorobiphenyls through Metal‐catalyzed CH Bond Activation/Arylation of (Poly)fluorobenzene Derivatives. Issue 7 (26th June 2014)
- Record Type:
- Journal Article
- Title:
- Synthesis of (Poly)fluorobiphenyls through Metal‐catalyzed CH Bond Activation/Arylation of (Poly)fluorobenzene Derivatives. Issue 7 (26th June 2014)
- Main Title:
- Synthesis of (Poly)fluorobiphenyls through Metal‐catalyzed CH Bond Activation/Arylation of (Poly)fluorobenzene Derivatives
- Authors:
- He, Mian
Soulé, Jean‐François
Doucet, Henri - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In recent years, palladium‐catalyzed direct arylation of (hetero)aromatics with aryl halides through a CH bond activation has become a popular method for generating carbon–carbon bonds. A wide variety of heteroaromatics such as furans, thiophenes, thiazoles, or even pyridines can be employed to prepare arylated heterocycles. Conversely, the formation of biphenyl derivatives through CH bond activation has attracted less attention, owing to the lower reactivity of CH bonds of most benzene derivatives. However, over the last few years several new results using modified and improved catalysts and reaction conditions, especially using polyfluorobenzene derivatives, have been reported permitting the synthesis of fluoro‐containing biphenyl derivatives at synthetically useful yields. As fluoro‐substituents on benzene rings appear to present a very specific effect, which promote such couplings, we summarize here the various methods allowing the synthesis of fluoro‐containing biaryls by metal‐catalyzed so called "direct arylation" of (poly)fluorobenzene derivatives. For most of these reactions, aryl halides have been used as the coupling partners, though a several examples employing other coupling partners, such as tosylates or boronic acids, are also known. Moreover, the reaction can be performed with several metal catalysts. This methodology allows the synthesis of complex molecules containing fluorine atoms<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In recent years, palladium‐catalyzed direct arylation of (hetero)aromatics with aryl halides through a CH bond activation has become a popular method for generating carbon–carbon bonds. A wide variety of heteroaromatics such as furans, thiophenes, thiazoles, or even pyridines can be employed to prepare arylated heterocycles. Conversely, the formation of biphenyl derivatives through CH bond activation has attracted less attention, owing to the lower reactivity of CH bonds of most benzene derivatives. However, over the last few years several new results using modified and improved catalysts and reaction conditions, especially using polyfluorobenzene derivatives, have been reported permitting the synthesis of fluoro‐containing biphenyl derivatives at synthetically useful yields. As fluoro‐substituents on benzene rings appear to present a very specific effect, which promote such couplings, we summarize here the various methods allowing the synthesis of fluoro‐containing biaryls by metal‐catalyzed so called "direct arylation" of (poly)fluorobenzene derivatives. For most of these reactions, aryl halides have been used as the coupling partners, though a several examples employing other coupling partners, such as tosylates or boronic acids, are also known. Moreover, the reaction can be performed with several metal catalysts. This methodology allows the synthesis of complex molecules containing fluorine atoms in only a few steps, and will certainly give the access to a very wide variety of new fluorinated biphenyls useful to both material and biochemists.</p> </abstract> … (more)
- Is Part Of:
- ChemCatChem. Volume 6:Issue 7(2014:Jul.)
- Journal:
- ChemCatChem
- Issue:
- Volume 6:Issue 7(2014:Jul.)
- Issue Display:
- Volume 6, Issue 7 (2014)
- Year:
- 2014
- Volume:
- 6
- Issue:
- 7
- Issue Sort Value:
- 2014-0006-0007-0000
- Page Start:
- 1824
- Page End:
- 1859
- Publication Date:
- 2014-06-26
- Subjects:
- Catalysis -- Periodicals
541.39505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cctc.201402020 ↗
- Languages:
- English
- ISSNs:
- 1867-3880
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3429.xml