Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2- a]carbazole Alkaloid Furoclausine-B

dc.contributor.author	Spindler B.
dc.contributor.author	Kataeva O.
dc.contributor.author	Knölker H.
dc.date.accessioned	2019-01-22T20:33:09Z
dc.date.available	2019-01-22T20:33:09Z
dc.date.issued	2018
dc.identifier.issn	0022-3263
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/147677
dc.description.abstract	© Copyright 2018 American Chemical Society. We describe the first enantioselective total synthesis and the assignment of the absolute configuration of the furo[3,2-a]carbazole alkaloid furoclausine-B. As key steps for our approach we used a palladium(II)-catalyzed double C-H-bond activation for the construction of the carbazole framework, a Shi epoxidation, and an intramolecular opening of the epoxide for annulation of the dihydrofuran moiety.
dc.relation.ispartofseries	Journal of Organic Chemistry
dc.title	Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2- a]carbazole Alkaloid Furoclausine-B
dc.type	Article
dc.relation.ispartofseries-issue	24
dc.relation.ispartofseries-volume	83
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	15136
dc.source.id	SCOPUS00223263-2018-83-24-SID85058567783

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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.