PHOTOELECTRON TRANSFER INDUCED DECARBOXYLATION OF SUBSTITUTED CARBOXYLIC-ACIDS ACROSS A LIQUID LIQUID INTERFACE/

Citation
Cs. Rajesh et al., PHOTOELECTRON TRANSFER INDUCED DECARBOXYLATION OF SUBSTITUTED CARBOXYLIC-ACIDS ACROSS A LIQUID LIQUID INTERFACE/, Tetrahedron, 53(49), 1997, pp. 16817-16834
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
53
Issue
49
Year of publication
1997
Pages
16817 - 16834
Database
ISI
SICI code
0040-4020(1997)53:49<16817:PTIDOS>2.0.ZU;2-M
Abstract
Methylene blue photocatalyzed electron transfer reactions of some phen oxyacetic acid derivatives and N-phenylglycine across a liquid/liquid interface led to their efficient decarboxylation. Nanosecond laser fla sh photolysis studies of this process. in a reverse micellar system of Aerosol-OT (AOT)-benzene-water indicated that the liquid/liquid inter face acts as a barrier in controlling the energy wasting back electron transfer. Intramolecular C-C bond forming reactions of these radicals were utilized for the synthesis of various chroman derivatives. (C) 1 997 Elsevier Science Ltd.