Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/21845
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.date.accessioned2022-11-10T12:20:17Z-
dc.date.available2022-11-10T12:20:17Z-
dc.date.issued2022-
dc.identifier.citationPelipko, V.V., Baichurin, R.I., Lyssenko, K.A., Dotsenko, V.V., Makarenko, S.V. A convenient synthesis of furo[3,2-c]pyran-3-carboxylates from 3-bromo-3-nitroacrylates // Mendeleev Communications. - 2022. - Том 32. - Выпуск 4. - Стр.: 454 - 456. - DOI10.1016/j.mencom.2022.07.009ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/21845-
dc.description.abstractNovel 4-oxo-4H-furo[3,2-c]pyran-3-carboxylates and 4-oxo- 4H-furo[3,2-c]chromene-3-carboxylates were prepared from available alkyl 3-bromo-3-nitroacrylates and 4-hydroxy-6- methyl-2H-pyran-2-one or 4-hydroxycoumarin, respectively. Their structures were confirmed by NMR and X-ray data.ru
dc.language.isoenru
dc.publisherElsevier Ltdru
dc.relation.ispartofseriesMendeleev Communications-
dc.subject1-halo-1-nitroethenesru
dc.subjectFuro[32-c]chromenesru
dc.subjectFuro[32-c]pyransru
dc.subjectHeterocyclizationru
dc.subjectNitroacrylatesru
dc.titleA convenient synthesis of furo[3,2-c]pyran-3-carboxylates from 3-bromo-3-nitroacrylatesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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