Issue 23, 2002
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Synthesis of [n]polynorbornanes with differing edge substitution: a new class of regioselectively addressable framework†

Frederick M. Pfeffer*a  and  Richard A. Russellb  

* Corresponding authors

a Department of Chemistry, Trinity College, Dublin, D2, Ireland
E-mail: pfefferf@tcd.ie.
Fax: +353 1 671 2826
Tel: +353 1 608 1306

b Centre for Chiral and Molecular Technologies, Deakin University, Geelong, 3216, Australia
E-mail: rarcat@deakin.edu.au.
Fax: +61 3 925 17492
Tel: +61 3 925 17454

Abstract

Polynorbornanes with differing edge functionality have been synthesised from the appropriate cyclobutene epoxides substituted with two, unlike, electron withdrawing groups. These latter compounds were prepared by the monohydrolysis of symmetric cyclobutene diesters and subsequent elaboration of the resulting carboxylic acid.

Graphical abstract: Synthesis of [n]polynorbornanes with differing edge substitution: a new class of regioselectively addressable framework

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Article information

DOI
https://doi.org/10.1039/B206057D
Article type
Paper
Submitted
24 Jun 2002
Accepted
17 Oct 2002
First published
05 Nov 2002

J. Chem. Soc., Perkin Trans. 1, 2002, 2680-2685

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Synthesis of [n]polynorbornanes with differing edge substitution: a new class of regioselectively addressable framework

F. M. Pfeffer and R. A. Russell, J. Chem. Soc., Perkin Trans. 1, 2002, 2680 DOI: 10.1039/B206057D

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