Preparation and Wittig reactions of organotrifluoroborato phosphonium ylides

Authors
Molander, Gary A.Ham, JungyeobCanturk, 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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