Issue 47, 2014

Alkyl transfer from C–C cleavage: replacing the nitro group of nitro-olefins

Abstract

Alkyl substituted Hantzsch esters are rationally used as alkylation reagents to replace the nitro groups of nitro olefins to give excellent yields of trans-olefins. The reaction mechanism is considered to proceed through a free radical mechanism, which is different from the corresponding transfer alkylation of imines.

Graphical abstract: Alkyl transfer from C–C cleavage: replacing the nitro group of nitro-olefins

Supplementary files

Article information

Article type
Communication
Submitted
12 Feb 2014
Accepted
17 Mar 2014
First published
17 Mar 2014

Chem. Commun., 2014,50, 6246-6248

Author version available

Alkyl transfer from C–C cleavage: replacing the nitro group of nitro-olefins

G. Li, L. Wu, G. Lv, H. Liu, Q. Fu, X. Zhang and Z. Tang, Chem. Commun., 2014, 50, 6246 DOI: 10.1039/C4CC01119H

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