Issue 2, 1991
From the journal:

Journal of the Chemical Society, Chemical Communications

Highly regio- and stereo-selective Diels–Alder reactions of 5-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)-1,4-naphthoquinone

Brian Beagley,   Anthony D. M. Curtis,   Robin G. Pritchard  and  Richard J. Stoodley  

Abstract

The title compound 1b reacts with cyclopentadiene to give a single cycloadduct, assigned the stereostructure 6a by X-ray crystallography; single cycloadducts, i.e.4c and d, also arise in the corresponding reactions involving the dienes 2b and c.

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Article information

DOI
https://doi.org/10.1039/C39910000119
Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 119-121

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Highly regio- and stereo-selective Diels–Alder reactions of 5-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)-1,4-naphthoquinone

B. Beagley, A. D. M. Curtis, R. G. Pritchard and R. J. Stoodley, J. Chem. Soc., Chem. Commun., 1991, 119 DOI: 10.1039/C39910000119

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