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Reactions of arylenedioxytrihalophosphoranes with acetylenes 14. Methoxyphenylacetylenes in the reaction with 2,2,2-trichlorobenzo-1,3,2-dioxaphosphole

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dc.contributor.author Nemtarev A.
dc.contributor.author Mironov V.
dc.contributor.author Aniskin A.
dc.contributor.author Baranov D.
dc.contributor.author Krivolapov D.
dc.contributor.author Musin R.
dc.contributor.author Vasilevskii S.
dc.date.accessioned 2018-09-19T20:57:01Z
dc.date.available 2018-09-19T20:57:01Z
dc.date.issued 2016
dc.identifier.issn 1066-5285
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/143461
dc.description.abstract © 2016, Springer Science+Business Media New York.Reactions of 2,2,2-trichlorobenzo-1,3,2-dioxaphosphole with 2-, 3-, 4-methoxyphenyl-, 3,4-dimethoxyphenyl- and 2,3,4-trimethoxyphenylacetylenes furnished 4-phenylbenzo-1,2-oxaphosphinine derivatives. The presence of one, two, or three donor methoxy groups in the aromatic ring of phenylacetylene does not change the general direction of the reaction which is characteristic of arylacetylenes and lead to 4-arylareno-1,2-oxaphosphinine derivatives. The presence of substituents in the exocyclic aryl group at ortho-position to the oxaphosphinine ring led to the appearance of atropoisomers.
dc.relation.ispartofseries Russian Chemical Bulletin
dc.subject 2,2,2-trichlorobenzo-1,3,2-dioxaphosphole
dc.subject atropoisomerism
dc.subject benzo-[e]-1,2-oxaphosphinine 2-oxides
dc.subject chlorination of aromatic ring
dc.subject formation of P—C bond
dc.subject ipso-substitution of oxygen
dc.subject methoxyphenylacetylenes
dc.title Reactions of arylenedioxytrihalophosphoranes with acetylenes 14. Methoxyphenylacetylenes in the reaction with 2,2,2-trichlorobenzo-1,3,2-dioxaphosphole
dc.type Article
dc.relation.ispartofseries-issue 5
dc.relation.ispartofseries-volume 65
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 1299
dc.source.id SCOPUS10665285-2016-65-5-SID85010693199


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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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