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

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]
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