Issue 17, 2017, Issue in Progress

Triflic acid promoted solvent free synthesis of densely functionalized furans

Abstract

A simple, efficient and novel methodology has been developed for the synthesis of densely substituted furans mediated by triflic acid. The current protocol proceeds in a domino fashion, the initial step involves Friedel–Crafts arylation, followed by dehydrative cyclization. It is operationally simple and can be carried out under solvent free conditions.

Graphical abstract: Triflic acid promoted solvent free synthesis of densely functionalized furans

Supplementary files

Article information

Article type
Paper
Submitted
12 Jan 2017
Accepted
30 Jan 2017
First published
07 Feb 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 10524-10528

Triflic acid promoted solvent free synthesis of densely functionalized furans

P. Vijayaprasad, A. Venkanna, M. Shanker, E. Kishan and P. Venkateswar Rao, RSC Adv., 2017, 7, 10524 DOI: 10.1039/C7RA00489C

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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