Issue 17, 2017, Issue in Progress
From the journal:

RSC Advances

Triflic acid promoted solvent free synthesis of densely functionalized furans†

Pulaganti Vijayaprasad,a   Avudoddi Venkanna,a   Medi Shanker,a   Eslavath Kishana  and  Pallapothula Venkateswar Rao ORCID logo *a  

* Corresponding authors

a Department of Chemistry, University College of Science, Osmania University, Tarnaka, Hyderabad 500007, India
E-mail: pallapothulavrao@gmail.com

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

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Article information

DOI
https://doi.org/10.1039/C7RA00489C
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

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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

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