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Role of aromatic substituent in the photochemical-reactions of naphthyl isoxazolines fused with saturated heterocyclic rings

P. Zálupský, Ľ. Fišera, and D. Hricová

Department of Organic Chemistry, Slovak Technical University, CS-812 37 Bratislava

 

Abstract: Character of aromatic substituent in the position 3 of 2-isoxazolines fused with the saturated heterocyclic rings in 4,5-position exerts strong influence on the outcome of the photochemical reaction. In contrast to phenyl-substituted isoxazolines those having a-naphthyl or 0-naphthyl substituents in position 3 are either photostable or suffer gradual photodestruction, depending on the UV radiation used.

Full paper in Portable Document Format: 405a707.pdf

 

Chemical Papers 40 (5) 707–715 (1986)

Monday, July 06, 2020

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