Becerra-Figueroa, L., Brun, E., Mathieson, M., Farrugia, L. J., Wilson, C. , Prunet, J. and Gamba-Sánchez, D. (2017) Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction. Organic and Biomolecular Chemistry, 15(2), pp. 301-305. (doi: 10.1039/C6OB02333A) (PMID:27897299)
|
Text
131841.pdf - Published Version Available under License Creative Commons Attribution. 987kB |
Abstract
A highly diastereoselective synthesis of trifluoromethylated 1,3-dioxanes is described. The reaction proceeds by an addition/oxa-Michael sequence and works efficiently under mild reaction conditions, with a good substrate scope and acceptable to good yields.
| Item Type: | Articles |
|---|---|
| Status: | Published |
| Refereed: | Yes |
| Glasgow Author(s) Enlighten ID: | Mathieson, Mr Michael and Farrugia, Dr Louis and Prunet, Dr Joelle and Wilson, Dr Claire |
| Authors: | Becerra-Figueroa, L., Brun, E., Mathieson, M., Farrugia, L. J., Wilson, C., Prunet, J., and Gamba-Sánchez, D. |
| College/School: | College of Science and Engineering > School of Chemistry |
| Journal Name: | Organic and Biomolecular Chemistry |
| Publisher: | Royal Society of Chemistry |
| ISSN: | 1477-0520 |
| ISSN (Online): | 1477-0539 |
| Published Online: | 23 November 2016 |
| Copyright Holders: | Copyright © 2017 The Royal Society of Chemistry |
| First Published: | First published in Organic and Biomolecular Chemistry 15(2):301-305 |
| Publisher Policy: | Reproduced under a Creative Commons License |
University Staff: Request a correction | Enlighten Editors: Update this record
Funder and Project Information
Funder and Project Information