Issue 7, 2002
From the journal:

Chemical Communications

Hydroformylation in fluorous solvents†

Douglas F. Foster,a   Dave J. Adams,b   David Gudmunsen,b   Alison M. Stuart,b   Eric G. Hopeb  and  David J. Cole–Hamiltona  

a Catalyst Evaluation and Optimisation Service, School of Chemistry, University of St. Andrews, Fife, Scotland, St. Andrews, UK
E-mail: djc@st-and.ac.uk

b Department of Chemistry, University of Leicester, Leicester, UK

Abstract

Triaryl-phosphines and -phosphites bearing fluorous ponytails give high rates, good linear selectivity and good retention of catalyst in the fluorous phase during hydroformylation of alkenes in fluorous solvents.

Graphical abstract: Hydroformylation in fluorous solvents

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Article information

DOI
https://doi.org/10.1039/B110061K
Article type
Communication
Submitted
05 Nov 2001
Accepted
22 Jan 2002
First published
06 Mar 2002

Chem. Commun., 2002, 722-723

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Hydroformylation in fluorous solvents

D. F. Foster, D. J. Adams, D. Gudmunsen, A. M. Stuart, E. G. Hope and D. J. Cole–Hamilton, Chem. Commun., 2002, 722 DOI: 10.1039/B110061K

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