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A stereospecific one-pot synthesis of β-chloro esters via the BiCl<inf>3</inf> catalysed O-acylative cleavage of crowded epoxides (2015)
Journal Article
Repetto, S. L., Costello, J. F., Lam, J., Ratcliffe, N. M., & Repetto, S. (2015). A stereospecific one-pot synthesis of β-chloro esters via the BiCl<inf>3</inf> catalysed O-acylative cleavage of crowded epoxides. Journal of Chemical Research, 39(6), 324-325. https://doi.org/10.3184/174751915X14322191328257

© 2015, Science Reviews 2000 Ltd. All rights reserved. A simple, one-pot procedure is described for the stereospecific preparation of β-chloro esters from the corresponding crowded epoxide.

Conformational analysis of triphenylphosphine ligands in stereogenic monometallic complexes: Tools for predicting the preferred configuration of the triphenylphosphine rotor (2015)
Journal Article
Gould, E. T., Costello, J. F., Davies, S. G., Gould, E., & Thomson, J. E. (2015). Conformational analysis of triphenylphosphine ligands in stereogenic monometallic complexes: Tools for predicting the preferred configuration of the triphenylphosphine rotor. Dalton Transactions, 44(12), 5451-5466. https://doi.org/10.1039/c5dt00250h

© The Royal Society of Chemistry 2015. The extension of our simple model for predicting the propeller configuration of a triphenylphosphine ligand co-ordinated to achiral metal centres to include stereogenic metal systems is described. By considerin... Read More about Conformational analysis of triphenylphosphine ligands in stereogenic monometallic complexes: Tools for predicting the preferred configuration of the triphenylphosphine rotor.