Issue 11, 2016

Ammonium catalyzed cyclitive additions: evidence for a cation–π interaction with alkynes

Abstract

The addition of carbamate nitrogen to a non-conjugated carbon–carbon triple bond is catalyzed by an ammonium salt leading to a cyclic product. Studies in homogeneous systems suggest that the ammonium agent facilitates nitrogen–carbon bond formation through a cation–π interaction with the alkyne unit that, for the first time, is directly observed by Raman spectroscopy.

Graphical abstract: Ammonium catalyzed cyclitive additions: evidence for a cation–π interaction with alkynes

Supplementary files

Article information

Article type
Communication
Submitted
18 Oct 2015
Accepted
22 Dec 2015
First published
23 Dec 2015

Chem. Commun., 2016,52, 2311-2313

Author version available

Ammonium catalyzed cyclitive additions: evidence for a cation–π interaction with alkynes

E. Nagy, E. St.Germain, P. Cosme, P. Maity, A. C. Terentis and S. D. Lepore, Chem. Commun., 2016, 52, 2311 DOI: 10.1039/C5CC08641H

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