On the Triple Role of Fluoride Ions in Palladium‐Catalyzed Stille Reactions. Issue 50 (9th November 2015)
- Record Type:
- Journal Article
- Title:
- On the Triple Role of Fluoride Ions in Palladium‐Catalyzed Stille Reactions. Issue 50 (9th November 2015)
- Main Title:
- On the Triple Role of Fluoride Ions in Palladium‐Catalyzed Stille Reactions
- Authors:
- Hervé, Marius
Lefèvre, Guillaume
Mitchell, Emily A.
Maes, Bert U. W.
Jutand, Anny - Abstract:
- Abstract: The mechanism of Stille reactions (cross‐coupling of ArX with Ar′Sn n Bu3 ) performed in the presence of fluoride ions is established. A triple role for fluoride ions is identified from kinetic data on the rate of the reactions of trans ‐[ArPdBr(PPh3 )2 ] (Ar=Ph, p ‐(CN)C6 H4 ) with Ar′SnBu3 (Ar′=2‐thiophenyl) in the presence of fluoride ions. Fluoride ions promote the rate‐determining transmetallation by formation of trans ‐[ArPdF(PPh3 )2 ], which reacts with Ar′SnBu3 (Ar′=Ph, 2‐thiophenyl) at room temperature, in contrast to trans ‐[ArPdBr(PPh3 )2 ], which is unreactive. However, the concentration ratio [F − ]/[Ar′SnBu3 ] must not be too high, because of the formation of unreactive anionic stannate [Ar′Sn(F)Bu3 ] − . This rationalises the two kinetically antagonistic roles exerted by the fluoride ions that are observed experimentally, and is found to be in agreement with the kinetic law. In addition, fluoride ions promote reductive elimination from trans ‐[ArPdAr′(PPh3 )2 ] generated in the transmetallation step. Abstract : Fluoride does the job : Three roles for fluoride ions in Stille reactions are identified from kinetic data. F − promotes the rate‐determining transmetallation by formation of trans ‐[ArPdF(PPh3 )2 ], which reacts with Ar′SnBu3, in contrast to trans ‐[ArPdBr(PPh3 )2 ], which does not. F − also promotes the reductive elimination in trans ‐[ArPdAr′(PPh3 )2 ]. However, the concentration ratio [F − ]/[Ar′SnBu3 ] must be less than 1 because of theAbstract: The mechanism of Stille reactions (cross‐coupling of ArX with Ar′Sn n Bu3 ) performed in the presence of fluoride ions is established. A triple role for fluoride ions is identified from kinetic data on the rate of the reactions of trans ‐[ArPdBr(PPh3 )2 ] (Ar=Ph, p ‐(CN)C6 H4 ) with Ar′SnBu3 (Ar′=2‐thiophenyl) in the presence of fluoride ions. Fluoride ions promote the rate‐determining transmetallation by formation of trans ‐[ArPdF(PPh3 )2 ], which reacts with Ar′SnBu3 (Ar′=Ph, 2‐thiophenyl) at room temperature, in contrast to trans ‐[ArPdBr(PPh3 )2 ], which is unreactive. However, the concentration ratio [F − ]/[Ar′SnBu3 ] must not be too high, because of the formation of unreactive anionic stannate [Ar′Sn(F)Bu3 ] − . This rationalises the two kinetically antagonistic roles exerted by the fluoride ions that are observed experimentally, and is found to be in agreement with the kinetic law. In addition, fluoride ions promote reductive elimination from trans ‐[ArPdAr′(PPh3 )2 ] generated in the transmetallation step. Abstract : Fluoride does the job : Three roles for fluoride ions in Stille reactions are identified from kinetic data. F − promotes the rate‐determining transmetallation by formation of trans ‐[ArPdF(PPh3 )2 ], which reacts with Ar′SnBu3, in contrast to trans ‐[ArPdBr(PPh3 )2 ], which does not. F − also promotes the reductive elimination in trans ‐[ArPdAr′(PPh3 )2 ]. However, the concentration ratio [F − ]/[Ar′SnBu3 ] must be less than 1 because of the formation of unreactive [Ar′Sn(F)Bu3 ] − . … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 50(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 50(2015)
- Issue Display:
- Volume 21, Issue 50 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 50
- Issue Sort Value:
- 2015-0021-0050-0000
- Page Start:
- 18401
- Page End:
- 18406
- Publication Date:
- 2015-11-09
- Subjects:
- fluoride -- kinetics -- palladium -- Stille reaction -- transmetallation
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201503309 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 846.xml