E-mail

E-mail a Wiley Online Library Link

Dr. Satoshi Mizuta, Oscar Galicia-López, Keary M. Engle, Stefan Verhoog, Dr. Katherine Wheelhouse, Dr. Gerasimos Rassias and Prof. Véronique Gouverneur Trifluoromethylation of Allylsilanes under Copper Catalysis Chemistry - A European Journal 18

Version of Record online: 12 JUN 2012 | DOI: 10.1002/chem.201201707

Thumbnail image of graphical abstract

Branched allylic CF3 products are accessible by copper-catalyzed trifluoromethylation of allylsilanes with the Togni reagent I. The silyl group is critical to control the outcome of this reaction because in its absence, a product of addition between the alkene and the Togni reagent is formed preferentially. The reaction is inhibited with 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) and is likely to operate via multiple reaction pathways.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field

SEARCH