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Direction and mechanism of the interaction of methyl(phenyl)selenyl chlorides with esters of 1,2alkadienephosphonic acids

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:6952432
This paper is a continuation of a study of the reactivity of organylselenyl chlorides with 1,2-alkadienephosphonates. The results are presented of a study of the interaction of methyl- and phenylselenyl chlorides with dialkyl esters of 3-mono- and 3,3-disubstituted 1,2-alkadiene-phosphonic acids. it is established that the direction of the reaction of the reaction of selenyl chlorides with esters of 1,2-alkadienephosphonic acids depends both on the nature of the substituents at the C/sup 3/ atom of the allene system and on the nture of the organic portion of the reagent. The reaction of esters of 3,3-disubstituted allenephosphonic acids with selenyl chlorides in a nonpolar solvent with cooling leads in all cases to five-membered heterocyclization of the allenephosphonate system.
Research Organization:
Higher Pedagogical Institute, Shumen
OSTI ID:
6952432
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 55:1,PT.1; ISSN JGCHA
Country of Publication:
United States
Language:
English