Intramolecular (4π+4π) Photocycloaddition via Naphthalene-Furan Exciplex
Author:
Affiliation:
1. Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823401103169432
Reference11 articles.
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2. J.J. McCullough, Chem. Rev., 87, 811 (1987)
3. A. Gilbert, Synthetic Organic Photochemistry, ed by W.M. Horspool, Plenum Press, New York, pp. 1-60 (1984)
4. R.A. Caldwell and D. Creed, Acc. Chem. Res., 1980, 13, 45.
5. Stereospecific (2π+2π) photocycloaddition of arylalkenes to pyrene via exciplex: formation of 1:1- and 2:1-cycloadducts
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1. Synthesis of Polycyclic Compounds by Using Photocycloaddition Reactions to Aromatic Rings;Journal of Synthetic Organic Chemistry, Japan;2018
2. Diastereoselective photocycloaddition reactions of 2-naphthalenecarboxylates and 2,3-naphthalenedicarboxylates with furans governed by chiral auxiliaries and hydrogen bonding interactions;Journal of Photochemistry and Photobiology A: Chemistry;2017-12
3. Hydrogen-bonding directed, regioselective photocycloaddition reactions of cyanonaphthalenes with furanmethanols;Photochemical & Photobiological Sciences;2011
4. ChemInform Abstract: Intramolecular (4π + 4π) Photocycloaddition via Naphthalene-Furan Exciplex.;ChemInform;2010-05-24
5. Formation of Caged Compounds in the Photocycloaddition of Furan to 2-, 2,3-, and 2,6-Substituted Naphthalenes via Dipole-Dipole Interaction;Journal of the Chinese Chemical Society;2006-02
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