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dc.contributor.author | Nemtarev A.V. | |
dc.contributor.author | Nasibullin I.O. | |
dc.contributor.author | Fayzullin R.R. | |
dc.contributor.author | Grigor'eva L.R. | |
dc.contributor.author | Mironov V.F. | |
dc.date.accessioned | 2021-02-25T20:35:52Z | |
dc.date.available | 2021-02-25T20:35:52Z | |
dc.date.issued | 2020 | |
dc.identifier.issn | 0959-9436 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/161941 | |
dc.description.abstract | © 2020 2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole reacts with arylacetylenes or 3-chloropropyne to give 2,7-dichloro-5-methoxy-4-aryl(haloalkyl)-1,2-benzoxaphosphinine 2-oxides. Hydrolysis of the latter leads to the opening of the oxaphosphinine ring and formation of (E)-2-(4-chloro-2- methoxy-6 hydroxyphenyl)ethenylphosphonic acid. | |
dc.relation.ispartofseries | Mendeleev Communications | |
dc.subject | arylacetylenes | |
dc.subject | cascade reactions | |
dc.subject | dioxaphospholes | |
dc.subject | ethenylphosphonic acids | |
dc.subject | oxaphosphinines | |
dc.subject | phosphoranes | |
dc.title | 2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole in the reactions with terminal acetylenes | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 1 | |
dc.relation.ispartofseries-volume | 30 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 34 | |
dc.source.id | SCOPUS09599436-2020-30-1-SID85079838791 |