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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

Repetto, Sonia L.; Costello, James F.; Lam, Joseph; Ratcliffe, Norman M.; Repetto, Sonia

A stereospecific one-pot synthesis of β-chloro esters via the BiCl<inf>3</inf> catalysed O-acylative cleavage of crowded epoxides Thumbnail


Authors

Sonia L. Repetto

Joseph Lam

Norman Ratcliffe Norman.Ratcliffe@uwe.ac.uk
Professor in Materials & Sensors Science

Sonia Repetto



Abstract

© 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.

Citation

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

Journal Article Type Article
Publication Date Jun 1, 2015
Deposit Date Jul 14, 2015
Publicly Available Date Mar 21, 2016
Journal Journal of Chemical Research
Publisher Science Reviews 2000
Peer Reviewed Peer Reviewed
Volume 39
Issue 6
Pages 324-325
DOI https://doi.org/10.3184/174751915X14322191328257
Keywords epoxides, stereospecific synthesis
Public URL https://uwe-repository.worktribe.com/output/833433
Publisher URL http://dx.doi.org/10.3184/174751915X14322191328257

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