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Reaction of dimethyl phosphite and monomethyl phenylphosphonite with 2-methyl-3,4,5-triphenylcyclopentadienone

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dc.contributor.author Arbuzov B.
dc.contributor.author Fuzhenkova A.
dc.contributor.author Galyautdinov N.
dc.date.accessioned 2018-09-14T20:38:45Z
dc.date.available 2018-09-14T20:38:45Z
dc.date.issued 1980
dc.identifier.issn 0568-5230
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/132606
dc.description.abstract In the absence of catalysts, the reaction of dimethyl phosphite and monomethyl phenylphosphonite with 2-methyl-3,4,5-triphenylcyelopentadienone goes with the formation of unconjugated β-phosphonoketones, which under the reaction conditions undergo prototropic isomerization to the conjugated β-phosphonoketones. In contrast to alcohols, dimethyl phosphite and monomethyl phenylphosphonite when reacted with the tricyclone do not form the products of 1,4-addition to the conjugated C=C-C=O system of the cyclone. © 1980 Plenum Publishing Corporation.
dc.relation.ispartofseries Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title Reaction of dimethyl phosphite and monomethyl phenylphosphonite with 2-methyl-3,4,5-triphenylcyclopentadienone
dc.type Article
dc.relation.ispartofseries-issue 4
dc.relation.ispartofseries-volume 29
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 651
dc.source.id SCOPUS05685230-1980-29-4-SID34250240412


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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