Organophosphorus chemistry,XII. Reaction of furil with alkyl phosphites and ylide-phosphoranes |
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Authors: | Mohamed R. Mahran Wafaa M. Abdou Maha D. Khidre |
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Affiliation: | (1) Department of Pesticide Chemistry, National Research Centre, Cairo, Egypt |
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Abstract: | Summary The reaction of furil (1) with trialkyl phosphites2 yielded caged phosphorane derivatives of types3a-c. Dry hydrogen chloride gas converted3a-c into the respectivea-hydroxyvinyl-phosphates8a-c which are equally produced by reacting furil with the appropriate dialkyl phosphite7. The reaction of furil with ylide-phosphoranes10 proceeded according to the Wittig reaction mechanism to give the respective ethylenes11a-c. The new compounds have been characterized by their spectroscopic data (IR, PMR,31P-NMR, MS) and elementary analyses.Dedicated to Prof. M. Sidky on the occasion of his 60th birthday |
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Keywords: | Furil a-Diketones Alkyl phosphites Caged phosphoranes Ylide-phosphoranes |
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