The anionic thia-Fries rearrangement of aryl triflates
Abstract
Aryl triflates undergo LDA-mediated rearrangement to generate o-hydroxyaryl trifluoromethylsulfones. In some cases, partitioning between rearrangement and
* Corresponding authors
a Structural Chemistry Laboratory, School of Chemistry, Cantock’s Close, Bristol, UK
b
Bristol Centre for Organometallic Catalysis, Cantock’s Close, Bristol, UK
E-mail:
guy.lloyd-jones@bris.ac.uk
Fax: 44 117 929 861
Tel: 44 117 928 8165
Aryl triflates undergo LDA-mediated rearrangement to generate o-hydroxyaryl trifluoromethylsulfones. In some cases, partitioning between rearrangement and
J. P. H. Charmant, A. M. Dyke and G. C. Lloyd-Jones, Chem. Commun., 2003, 380 DOI: 10.1039/B210648E
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