Issue 31, 2015

Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO

Abstract

A novel and convenient metal-free nitration and cyclization of 1,6-enynes has been developed. Two C–C bonds and one C–N bond were constructed in one process in this reaction. This transformation is proven to have relatively good functional-group applicability and can be scaled up to gram quantities in satisfactory yields. According to the following experimental facts and related literature reports, a radical pathway was involved in this transformation.

Graphical abstract: Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2015
Accepted
11 Mar 2015
First published
12 Mar 2015

Chem. Commun., 2015,51, 6839-6842

Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO

X. Hao, P. Gao, X. Song, Y. Qiu, D. Jin, X. Liu and Y. Liang, Chem. Commun., 2015, 51, 6839 DOI: 10.1039/C5CC00872G

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