Intramolecular Through-Space Interaction in 2-(p-Methoxyphenyl)-2-butenyl 9-Phenanthrenecarboxylate as Evidenced by Their Isomerization Behavior
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/4/66_4_1312/_pdf
Reference14 articles.
1. Conformations and competitive [2 + 2] cycloadditions of intramolecular exciplexes of some anisylalkenyl 9-phenanthrenecarboxylates
2. Photochemical and Photophysical Behavior ofp-Methoxyphenyl alkenyl Phenanthrenecarboxylates. I. Structure and Competitive Formation of Intramolecular Cycloaddition Products
3. Photochemical and Photophysical Behavior ofp-Methoxyphenylalkenyl Phenanthrenecarboxylates. II. Kinetic Investigation of Intramolecular Cycloaddition
4. Photochemical Cycloaddition of Phenanthrene-Fused Lactones to (E)-Anethole. Structural Effects and Dual Collapse Processes of an Exciplex Leading to Cycloadducts.
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2. Photochemical behaviour of poly(vinyl alcohol) bearing p-phenylenediacrylate groups;Polymer;1998-01
3. Self-Sensitized Photolysis ofN-(1-Naphthoyl)-N-phenyl-O-(benzoyl-substituted benzoyl)hydroxylamines;Bulletin of the Chemical Society of Japan;1996-09
4. Enhancement of reactivity of the ester carbonyl group by interchromophoric links in photochemical cycloadditions. Intermediacy and roles of plural intramolecular exciplexes;Research on Chemical Intermediates;1995-08
5. Intramolecular Photochemical Cycloaddition of Arenecarboxylic Esters Involving Carbonyl Addition.;Journal of Synthetic Organic Chemistry, Japan;1994
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