Issue 99, 2014

Oxidative cross-dehydrogenative coupling between N-aryl tetrahydroisoquinolins and 5H-oxazol-4-ones through two methodologies: copper catalysis or a metal-free strategy

Abstract

A direct oxidative cross-dehydrogenative coupling (CDC) of N-aryl tetrahydroisoquinolins with 5H-oxazol-4-ones catalyzed by CuBr using air as the only oxidant has been developed, which could also proceed smoothly under a metal-free oxidative system with PhI(OAc)2 as the oxidant. A series of alkylated tetrahydroisoquinolin derivatives were obtained in good yields and excellent diastereoselectivities.

Graphical abstract: Oxidative cross-dehydrogenative coupling between N-aryl tetrahydroisoquinolins and 5H-oxazol-4-ones through two methodologies: copper catalysis or a metal-free strategy

Supplementary files

Article information

Article type
Communication
Submitted
13 Jun 2014
Accepted
16 Oct 2014
First published
23 Oct 2014

Chem. Commun., 2014,50, 15714-15717

Oxidative cross-dehydrogenative coupling between N-aryl tetrahydroisoquinolins and 5H-oxazol-4-ones through two methodologies: copper catalysis or a metal-free strategy

X. Liu, J. Zhang, S. Ma, Y. Ma and R. Wang, Chem. Commun., 2014, 50, 15714 DOI: 10.1039/C4CC04508D

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