Three step synthesis of single diastereoisomers of the vicinal trifluoro motif
MetadataShow full item record
A three step route to single diastereoisomers of the vicinal trifluoromethyl motif is described. The route starts from either syn- or anti-alpha,beta-epoxy alcohols and takes a direct approach in that each of the three steps introduces a fluorine atom in a regio- and stereospecific manner. Starting from either the syn- or the anti-alpha,beta-epoxy alcohol, stereospecific reactions generate two separate diastereoisomeric series of this motif. The route is a significant improvement on an earlier six step strategy.
Brunet , V A , Slawin , A M Z & O'Hagan , D 2009 , ' Three step synthesis of single diastereoisomers of the vicinal trifluoro motif ' Beilstein Journal of Organic Chemistry , vol. 5 , 61 . https://doi.org/10.3762/bjoc.5.61
Beilstein Journal of Organic Chemistry
© 2009 Brunet et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)
Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.