Issue 20, 2013

Transition-metal catalyst free C[double bond, length as m-dash]N coupling with phenol/phenoxide: a green synthesis of a benzoxazole scaffold by an anodic oxidation reaction

Abstract

By utilizing an anodic oxidative reaction and consuming 2.2 F mol−1 of electricity, C[double bond, length as m-dash]N coupling with phenol/phenoxide to obtain the five-membered N,O-heteroatom ring of a benzoxazole has been achieved at room temperature. Transition-metal catalysts, chemical oxidants, strong acids, reactive chemical reagents and refluxing are not required. Studies of the electrode, solvent, electrolyte and additive effects to promote the anodic cyclization are included. From the CV studies, the reaction mechanisms of the anodic cyclization are proposed.

Graphical abstract: Transition-metal catalyst free C [[double bond, length as m-dash]] N coupling with phenol/phenoxide: a green synthesis of a benzoxazole scaffold by an anodic oxidation reaction

Supplementary files

Article information

Article type
Paper
Submitted
09 Jan 2013
Accepted
20 Feb 2013
First published
27 Feb 2013

RSC Adv., 2013,3, 7330-7336

Transition-metal catalyst free C[double bond, length as m-dash]N coupling with phenol/phenoxide: a green synthesis of a benzoxazole scaffold by an anodic oxidation reaction

Y. Shih, C. Ke, C. Pan and Y. Huang, RSC Adv., 2013, 3, 7330 DOI: 10.1039/C3RA00128H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements