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Exploration of the Fluoride Reactivity of Aryltrifluoroborate on Selective Cleavage of Diphenylmethylsilyl Groups

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dc.contributor.author Fujiki K.
dc.contributor.author Tanaka K.
dc.date.accessioned 2021-02-25T20:43:03Z
dc.date.available 2021-02-25T20:43:03Z
dc.date.issued 2020
dc.identifier.issn 1434-193X
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/162289
dc.description.abstract © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim The first known report on the fluoride catalytic reactivity of potassium aryltrifluoroborate is described. The fluoride reactivity of phenyltrifluoroborate was controlled by substituents on the trifluoroborate-attached benzene, such as the methoxy group at the para-position and the methyl group at the ortho-position. In addition, the selective aryltrifluoroborate-catalyzed cleavage of the diphenylmethylsilyl group was achieved.
dc.relation.ispartofseries European Journal of Organic Chemistry
dc.subject Desilylation
dc.subject Fluorides
dc.subject Organocatalysis
dc.subject Reaction mechanisms
dc.subject Trifluoroborates
dc.title Exploration of the Fluoride Reactivity of Aryltrifluoroborate on Selective Cleavage of Diphenylmethylsilyl Groups
dc.type Article
dc.relation.ispartofseries-issue 29
dc.relation.ispartofseries-volume 2020
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 4616
dc.source.id SCOPUS1434193X-2020-2020-29-SID85087288692


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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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