Issue 35, 2015

Synthesis of a new class of iminosugars based on constrained azaspirocyclic scaffolds by way of catalytic C–H amination

Abstract

The synthesis of the first examples of a new class of iminosugars based on constrained spirocyclic scaffolds has been achieved via Rh-catalyzed C(sp3)–H amination. In this process, the needed electronic control in securing high regioselectivity from substrates with a high density of activated C–H bonds was achieved by using a combination of activating and electron-withdrawing groups.

Graphical abstract: Synthesis of a new class of iminosugars based on constrained azaspirocyclic scaffolds by way of catalytic C–H amination

Supplementary files

Article information

Article type
Communication
Submitted
18 Jun 2015
Accepted
02 Jul 2015
First published
03 Jul 2015

Org. Biomol. Chem., 2015,13, 9176-9180

Author version available

Synthesis of a new class of iminosugars based on constrained azaspirocyclic scaffolds by way of catalytic C–H amination

P. Nocquet, R. Hensienne, J. Wencel-Delord, E. Wimmer, D. Hazelard and P. Compain, Org. Biomol. Chem., 2015, 13, 9176 DOI: 10.1039/C5OB01254F

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