Donor–Acceptor Binary Photocatalysis System Illustrated by the Intramolecular Cyclization of a Cyclopropanone Acetal Tethered to Cyclohexen-2-one
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/72/3/72_3_511/_pdf
Reference39 articles.
1. Oxidative Ring-Opening Reaction of Cyclopropanone Acetals with Carbonyl Compounds via Photoinduced Electron Transfer. Generation of a .beta.-Carbonyl Radical Species and Its Application to the Synthesis of .gamma.-Hydroxy Ester Derivatives
2. Ring-opening addition reaction of cyclopropanol derivatives with carbenes
3. Formation of unsaturated esters in the single electron transfer reaction of cyclopropanone acetals with quinones under non-irradiated conditions
4. Electron Transfer Profile of Cyclopropanone Acetals in the Nonirradiated Reaction with Tetracyanoethylene, Chloranil, and Dicyanodichlorobenzoquinone
5. A unique stereospecific [.pi.2s + .sigma.2a] cycloaddition of tetracyanoethylene to substituted cyclopropanone acetals
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1. Photochemical Generation of Radical Ions;Photochemically-Generated Intermediates In Synthesis;2013-07-12
2. ChemInform Abstract: Donor-Acceptor Binary Photocatalysis System Illustrated by the Intramolecular Cyclization of a Cyclopropanone Acetal Tethered to Cyclohexen-2-one.;ChemInform;2010-06-14
3. Efficient photochemical electron transfer sensitization of homogeneous organic reactions;Journal of Photochemistry and Photobiology C: Photochemistry Reviews;2008-06
4. Electron Transfer Promoted Regioselective Ring-Opening Reaction of Cyclopropyl Silyl Ethers;Organic Letters;2007-06-27
5. Photocatalysis for the Formation of the C−C Bond;Chemical Reviews;2007-05-27
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