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The B(C6F5)3-Catalyzed Tandem Meinwald Rearrangement-Reductive Amination

ISSN
1523-7060
Date Issued
2016
Author(s)
Tiddens, Martine R.
Klein Gebbink, Robertus J. M.
Otte, Matthias 
DOI
10.1021/acs.orglett.6b01744
Abstract
A system of three coupled catalytic cycles enabling the one-pot transformation of epoxides to amines via Meinwald rearrangement, imine condensation, and imine reduction is described. This assisted tandem catalysis is catalyzed by B(C6F5)3 resulting in the first tandem Meinwald rearrangement-reductive amination protocol. The reaction proceeds in nondried solvents and yields β-functionalized amines. In particular, β-diarylamines are obtained in high yields.
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