Photooxygenation of 1,2-dihydronaphthalenes resulted in diendoperoxides and hydroperoxides via [ 4 + 2 ] cycloaddition and ene reactions, respectively. The relative conΓguration and stereochemistry of the products were elucidated by various 1H and 13C NMR methods.
The Mass Spectral Analyses of 2-Sila-1,2-dihydronaphthalene Derivatives
β Scribed by Taewook Kim; Chang Hwan Kim; Myong Euy Lee; Dae-Jei Bang; Soo-Dong Yoh; Young-Woo Kwak
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 412 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0951-4198
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β¦ Synopsis
Mass spectral analyses of 2-sila-l,2-dihydronaphthalene derivatives are reported. The 2-silanaphthalene radical cations, Zsilanaphthyl cation, 1-sifaindenyl cation, indene radical cation, and indenyl cation were proposed among the fragments of these molecules. The important fragmentation pathways consist of @-elimination of a molecule which includes the substituent on silicon, elimination of carbenes and elimination of silylenes.
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