Issue 54, 2016

Peroxodisulfate-mediated selenoamination of alkenes yielding amidoselenide-containing sulfamides and azoles

Abstract

A new protocol for C–Se and C–N bond formation by the direct difunctionalization of alkenes is reported. The protocol is operationally simple, has a wide substrate scope, and uses readily available amino sources. This reaction represents a significant addition to the limited number of intermolecular selenide difunctionalization reactions of alkenes and would find practical application in the synthesis of nitrogen- and selenium-containing molecules.

Graphical abstract: Peroxodisulfate-mediated selenoamination of alkenes yielding amidoselenide-containing sulfamides and azoles

Supplementary files

Article information

Article type
Communication
Submitted
19 May 2016
Accepted
07 Jun 2016
First published
08 Jun 2016

Chem. Commun., 2016,52, 8471-8474

Peroxodisulfate-mediated selenoamination of alkenes yielding amidoselenide-containing sulfamides and azoles

K. Sun, X. Wang, Y. Lv, G. Li, H. Jiao, C. Dai, Y. Li, C. Zhang and L. Liu, Chem. Commun., 2016, 52, 8471 DOI: 10.1039/C6CC04225B

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