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
โ 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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๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
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(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