Issue 17, 2001
From the journal:

Chemical Communications

Oxidative cyclisation of cinnamyl ethers mediated by CAN: a stereoselective synthesis of 3,4-trans disubstituted tetrahydrofuran derivatives

Vijay Nair,*a   Lakshmi Balagopal,a   V. Sheeba,a   Sreeletha B. Panickera  and  Nigam P. Rathb  

* Corresponding authors

a Organic Chemistry Division, Regional Research Laboratory (CSIR), Trivandrum, India.
E-mail: gvn@csrrltrd.ren.nic.in;
Fax: +91-471-491712

b Department of Chemistry, The University of Missouri, St Louis, MO 63121-4499, USA

Abstract

The oxidative cyclisation of cinnamyl ethers mediated by cerium(IV) ammonium nitrate results in the stereospecific formation of 3,4-trans disubstituted tetrahydrofuran derivatives in moderate to good yields.

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Article information

DOI
https://doi.org/10.1039/B103111M
Article type
Communication
Submitted
05 Apr 2001
Accepted
06 Jul 2001
First published
16 Aug 2001

Chem. Commun., 2001, 1682-1683

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Oxidative cyclisation of cinnamyl ethers mediated by CAN: a stereoselective synthesis of 3,4-trans disubstituted tetrahydrofuran derivatives

V. Nair, L. Balagopal, V. Sheeba, S. B. Panicker and N. P. Rath, Chem. Commun., 2001, 1682 DOI: 10.1039/B103111M

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