Issue 5, 2018, Issue in Progress

The synthesis of some novel stilbene dimers incorporating diamide tethers: studies in single electron transfer oxidation (FeCl3)

Abstract

The FeCl3 oxidative cascade reaction of the acetamido stilbene 1 which we reported some years ago produced the first atropodiastereomeric indolostilbene hybrid 3. By contrast, recent investigation of the oxidation of the stilbene succinamide dimer 72 (FeCl3/CH2Cl2) appears, on the basis of spectroscopic evidence, to have produced the bridged macrocyclic indoline 73.

Graphical abstract: The synthesis of some novel stilbene dimers incorporating diamide tethers: studies in single electron transfer oxidation (FeCl3)

Supplementary files

Article information

Article type
Paper
Submitted
17 Nov 2017
Accepted
25 Dec 2017
First published
11 Jan 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 2506-2520

The synthesis of some novel stilbene dimers incorporating diamide tethers: studies in single electron transfer oxidation (FeCl3)

M. S. Alehashem, A. Ariffin, A. A. Qatran Al-Khdhairawi and N. F. Thomas, RSC Adv., 2018, 8, 2506 DOI: 10.1039/C7RA12534H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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