Ring Expansion through [2+2] Photocycloaddition–β-Scission Sequence. Two Carbon Ring Expansions of β-Indanone and β-Tetralone
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference5 articles.
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1. Asymmetric synthesis of tricyclic tetralin derivatives via an intramolecular photoreaction;Tetrahedron;2007-07
2. Photoinduced molecular transformations. Part 152. Ring expansion based on a sensitized [2 + 2] photoaddition of enol ethers of cyclic ketones with olefins, followed by a β-scission of alkoxyl radicals generated from the resulting cyclobutanols. Two-carbon ring expansion of β-indanone, β-tetralone and β-suberone;J. Chem. Soc., Perkin Trans. 1;1995
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4. Introduction of Different Groups to α- and β-Positions of Cyclic α,β-Unsaturated Ketones via [2π + 2π] Photocycloaddition with Ketene Silyl Acetals Followed by Electrode Reaction;Chemistry Letters;1994-07
5. Photoinduced molecular transformations. Part 150. A new total synthesis of (±)-α-Himachalene based on a Sequence involving [2+2] photoaddition and regioselective β-scission of alkoxyl radicals generated from the resulting cyclobutanols;Tetrahedron;1994-01
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