Iminophosphine-palladium(0) complexes as catalysts in the alkoxycarbonylation of terminal alkynes
✍ Scribed by A Scrivanti; U Matteoli; V Beghetto; S Antonaroli; R Scarpelli; B Crociani
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 91 KB
- Volume
- 170
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
In the presence of methanesulfonic acid, the palladium(0)-olefin complexes: [Pd( 2 -ol)(P-N)] [ol = dimethyl fumarate or fumaronitrile, P-N = 1-(Ph 2 P)C 6 H 4 -2-CH=NR (R = CMe 3 or C 6 H 4 OMe-4)] catalyse the alkoxycarbonylation of terminal alkynes. Moderately good rates are obtained when the catalysts are promoted with two equivalents of the free P-N ligand and a large excess of acid at 120 • C. The catalytic data suggest that derivatives of the type [Pd(alkyne)(P-N) n ] (n = 2-3) are the active catalytic species.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
2-Furyl)phenyl(2-pyridyl)phosphine has been synthesised by reaction of 2-furyllithium with chlorophenyl(2-pyridyl)phosphine. The new ligand in combination with Pd(OAc) 2 and methanesulphonic acid provides a catalytic system highly active in the alkoxycarbonylation of terminal alkynes. The catalytic