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Tributylphosphine catalyzed addition of diphenylphosphine oxide to unsubstituted and substituted electron-deficient alkenes

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dc.date.accessioned 2019-01-22T20:34:51Z
dc.date.available 2019-01-22T20:34:51Z
dc.date.issued 2018
dc.identifier.issn 0040-4039
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/147800
dc.description.abstract © 2018 Elsevier Ltd The PBu3-catalyzed conjugate addition of diphenylphosphine oxide to unsubstituted and substituted electron-deficient alkenes is reported. β-Substituted α,β-unsaturated esters, trans-methyl crotonate and trans-methyl cinnamate, known for their reluctance to participate in phosphine-catalyzed transformations, also react well under the developed conditions. Mild reaction conditions, simple work-up and the ease of catalyst recovery make the proposed methodology useful for the preparation of functionalized tertiary phosphine oxides. The utility of this method was demonstrated by the gram-scale reactions of diphenylphosphine oxide with electron-deficient alkenes.
dc.relation.ispartofseries Tetrahedron Letters
dc.subject Phospha-Michael addition
dc.subject Phosphine organocatalysis
dc.subject Pudovik reaction
dc.subject X-ray analysis
dc.title Tributylphosphine catalyzed addition of diphenylphosphine oxide to unsubstituted and substituted electron-deficient alkenes
dc.type Article
dc.relation.ispartofseries-issue 17
dc.relation.ispartofseries-volume 59
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 1630
dc.source.id SCOPUS00404039-2018-59-17-SID85044333953


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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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