ChemInform Abstract: NITROSOALKENES: SYNTHESIS AND REACTIVITY

Autor: Heinz-Günther Viehe, E. Francotte, Robert Merényi, B. Vandenbulcke-Coyette
Rok vydání: 1981
Předmět:
Zdroj: Chemischer Informationsdienst. 12
ISSN: 0009-2975
DOI: 10.1002/chin.198142151
Popis: Some α- and β-halonitrosoalkenes 1 have been synthesized and characterized. The halogen atoms of the oxime precursors 2 can be substituted by alkoxy groups. Two kinds of cycloaddition reaction of 1 have been observed: (i) reaction of the NO group with dienes gives 3, 6-dihydrooxazine derivatives 6 which isomerise to epoxyepimines 7 in most cases of β-substituted nitrosoalkenes; (ii) if 4, 5-dihydrooxazines 22 are obtained, the cycloaddition of the nitrosoalkenes as 4π-component is presumed.
Databáze: OpenAIRE