Issue 23, 2016

Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides

Abstract

A mild and efficient methodology involving the I2/TBHP-mediated intermolecular iodoamination of ynamides with amines for the synthesis of α-amino-β,β-diiodo-enamides was developed. This reaction provides the first intermolecular iodoamination of terminal alkynes to diiodo-enamines and can be easily applied to a wide range of substrates.

Graphical abstract: Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides

Supplementary files

Article information

Article type
Communication
Submitted
14 Jan 2016
Accepted
10 Feb 2016
First published
10 Feb 2016

Chem. Commun., 2016,52, 4321-4324

Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides

H. Huang, L. Tang, X. Han, G. He, Y. Xi and H. Zhu, Chem. Commun., 2016, 52, 4321 DOI: 10.1039/C6CC00370B

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