Electron transfer oxidation of enol derivatives of 2,3-dihydrobenzopyran-4-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Photosensitized (set) conversion of 2′-hydroxychalcones to flavonoids a probable biogenetic pathway
2. Photosensitized Dehydrogenation of Flavanones to Flavones Using 2,4,6-Triphenylpyrylium Tetrafluoroborate (TPT)
3. Photolysis of cyclic enol esters in the presence or absence of a single electron transfer photosensitizer
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1. ChemInform Abstract: Electron Transfer Oxidation of Enol Derivatives of 2,3- Dihydrobenzopyran-4-ones.;ChemInform;2010-08-18
2. Chemical and transient spectroscopic evidence for radical and ionic pathways in the photolysis of 3-halo-2,3-dihydrobenzopyran-4-ones;Arkivoc;2007-01-08
3. Studies on Regioselectivity of Nitration of Coumarins with Cerium(IV) Ammonium Nitrate: Solid-State Nitration of 6-Hydroxy-Coumarins on Montmorillonite K-10 Clay Support Under Microwave Irradiation;Synthetic Communications;2003-01-04
4. Influence of the intrazeolite microenvironment on the fate of the radical pairs formed by photolysis of 3-bromo-4-chromanone;Journal of Photochemistry and Photobiology A: Chemistry;1995-02
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