Synthesis of Dioxa-Cages as a New Probe for the Stereochemistry of the Bisadducts ofp-Quinone with Cyclopentadiene and Cyclohexadiene
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jccs.199800120/fullpdf
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4. Unusual stereoselectivity in the Diels-Alder addition of cyclopentadiene with the bicyclo[2.2.2]octene nucleus
5. Aromatic ring-system controls π-facial selectivity in Diels-Alder reactions of [3.3]orthoanthracenophanes
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3. Synthesis of new acetal aza-cage compounds via ozonolysis of bis-endo-diol- and diacylnorbornene derivatives;Tetrahedron;2012-03
4. Alkyl radical cyclization to vinylogous carbonates for the stereoselective synthesis of unsymmetrical dioxa-cage compounds: effect of conformation on the rate of cyclization versus reduction;Tetrahedron;2011-02
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