Preparation and Wittig reactions of organotrifluoroborato phosphonium ylides
- Authors
- Molander, Gary A.; Ham, Jungyeob; Canturk, Belgin
- Issue Date
- 2007-03-01
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.9, no.5, pp.821 - 824
- Abstract
- Potassium [(trifluoroboratophenyl)methyl]triphenylphosphonium chlorides have been prepared from the corresponding benzyl chlorides and PPh3. In the presence of 1.2 equiv of K2CO3 and various aldehydes, these mixed salts are easily converted to the corresponding unsaturated organotrifluoroborates via the intermediate phosphorus ylides. A protocol for a one-pot transformation has also been developed.
- Keywords
- CROSS-COUPLING REACTIONS; AMINO-ACIDS; SUZUKI; BROMIDES; CROSS-COUPLING REACTIONS; AMINO-ACIDS; SUZUKI; BROMIDES; Organotrifluoroborate; Wittig Reaction; Olefination; Suzuki-Miyaura cross-coupling
- ISSN
- 1523-7060
- URI
- https://pubs.kist.re.kr/handle/201004/134548
- DOI
- 10.1021/ol063043e
- Appears in Collections:
- KIST Article > 2007
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