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Issue 22, 2000
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A density functional theory study of π-facial stereoselectivity in intramolecular Diels–Alder reactionsElectronic supplementary information (ESI) available: final optimised coordinates for stationary points in all transition structures. See http://www.rsc.org/suppdata/cc/b0/b006486f/

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Abstract

B3LYP/6-31G(d) theory has been used to construct a transition structure model which correctly accounts for the observed π-diastereofacial selectivity in intramolecular Diels-Alder reactions induced by allylic substituents attached to the diene.

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Supplementary files

Article information


Submitted
08 Aug 2000
Accepted
27 Sep 2000
First published
31 Oct 2000

Chem. Commun., 2000, 2215-2216
Article type
Communication

A density functional theory study of π-facial stereoselectivity in intramolecular Diels–Alder reactions

M. N. Paddon-Row and M. S. Sherburn, Chem. Commun., 2000, 2215
DOI: 10.1039/B006486F

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