STRUCTURE ELUCIDATION OF THE PHOTOOXYGENATION PRODUCTS OF 1,2-DIHYDRONAPHTHALENES

Authors
TOTH G LINKER T REBIEN F
Citation
G. Toth et al., STRUCTURE ELUCIDATION OF THE PHOTOOXYGENATION PRODUCTS OF 1,2-DIHYDRONAPHTHALENES, Magnetic resonance in chemistry, 35(6), 1997, pp. 367-371
Citations number
16
Categorie Soggetti
Spectroscopy,Chemistry
Journal title
Magnetic resonance in chemistry → ACNP
ISSN journal
07491581
Volume
35
Issue
6
Year of publication
1997
Pages
367 - 371
Database
ISI
SICI code
0749-1581(1997)35:6<367:SEOTPP>2.0.ZU;2-0
Abstract
Photooxygenation of 1,2-dihydronaphthalenes resulted in diendoperoxide s and hydroperoxides via [4 + 2] cycloaddition and ene reactions, resp ectively, The relative configuration and stereochemistry of the produc ts were elucidated by various H-1 and C-13 NMR methods. (C) 1997 by Jo hn Wiley & Sons, Ltd.