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P( i -BuNCH 2 CH 2 ) 3 N: An Efficient Promoter for the Nucleophilic Aromatic Substitution Reaction of Aryl Fluorides with Aryl TBDMS (or TMS) Ethers

โœ Scribed by Urgaonkar, Sameer; Verkade, John G.


Book ID
126124479
Publisher
American Chemical Society
Year
2005
Tongue
English
Weight
92 KB
Volume
7
Category
Article
ISSN
1523-7060

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๐Ÿ“œ SIMILAR VOLUMES


P(i-BuNCH2CH2)3N: an efficient promoter
โœ Steven M. Raders; John G. Verkade ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 154 KB

With the title proazaphosphatrane as a promoter, the coupling of aryl fluorides with aryl TBDMS ethers under microwave conditions gave moderate to high yields of the desired products at low catalyst loadings and in short times. In this methodology, electron deficient aryl fluorides possessing substi

Pd/P(i-BuNCH2CH2)3N: an efficient cataly
โœ Sameer Urgaonkar; M. Nagarajan; J.G. Verkade ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 123 KB

Pd(OAc) 2 in combination with the commercially available ligand P(i-BuNCH 2 CH 2 ) 3 N catalyzes the Suzuki cross-coupling reaction of a wide variety of aryl bromides and chlorides with arylboronic acids, affording the desired biaryls in excellent yields. It has also been shown that P(NMe 2 ) 3 can