The pathway of the palladium catalysed methoxycarbonylation of ethene to methyl propanoate has been shown to occur via a hydride rather than a methoxycarbonyl cycle and all the intermediates in this cycle have been unambiguously identified by multinuclear NMR spectroscopy and 13C- labelling.

Synthesis and spectroscopic characterisation of all the intermediates in the Pd-catalysed methoxycarbonylation of ethene / Eastham G.R.; Heaton B.T.; Iggo J.A.; Tooze R.P.; Whyman R.; Zacchini S.. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 2000:7(2000), pp. 609-610. [10.1039/b001110j]

Synthesis and spectroscopic characterisation of all the intermediates in the Pd-catalysed methoxycarbonylation of ethene

Zacchini S.
2000

Abstract

The pathway of the palladium catalysed methoxycarbonylation of ethene to methyl propanoate has been shown to occur via a hydride rather than a methoxycarbonyl cycle and all the intermediates in this cycle have been unambiguously identified by multinuclear NMR spectroscopy and 13C- labelling.
2000
Synthesis and spectroscopic characterisation of all the intermediates in the Pd-catalysed methoxycarbonylation of ethene / Eastham G.R.; Heaton B.T.; Iggo J.A.; Tooze R.P.; Whyman R.; Zacchini S.. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 2000:7(2000), pp. 609-610. [10.1039/b001110j]
Eastham G.R.; Heaton B.T.; Iggo J.A.; Tooze R.P.; Whyman R.; Zacchini S.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/937949
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