Tetraalkynylstannanes in the stille cross coupling reaction: a new effective approach to arylalkynes

Dotsenko, V. V.; Доценко, В. В.

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3040

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DC Field	Value	Language
dc.contributor.author	Dotsenko, V. V.	-
dc.contributor.author	Доценко, В. В.	-
dc.date.accessioned	2018-09-21T09:36:26Z	-
dc.date.available	2018-09-21T09:36:26Z	-
dc.date.issued	2017	-
dc.identifier.citation	Levashov, A.S., Buryi, D.S., Goncharova, O.V., Konshin, V.V., Dotsenko, V.V., Andreev, A.A. Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes // New Journal of Chemistry. - 2017. - Volume 41. - Issue 8. - Pages 2910-2918	ru
dc.identifier.uri	https://www.scopus.com/record/display.uri?eid=2-s2.0-85017324547&origin=resultslist&sort=plf-f&src=s&st1=Tetraalkynylstannanes+in+the+Stille+cross+&st2=&sid=97089f1e058ec08e3dec0b149bd56c66&sot=b&sdt=b&sl=57&s=TITLE-ABS-KEY%28Tetraalkynylstannanes+in+the+Stille+cross+%29&relpos=0&citeCnt=3&searchTerm=	-
dc.identifier.uri	http://hdl.handle.net/20.500.12258/3040	-
dc.description.abstract	The Stille-type cross coupling reaction with tetraalkynylstannanes was studied in detail for the first time. The reaction provides a simple and effective route towards a variety of arylalkynes. The advantages and limitations of the proposed procedure are discussed	ru
dc.language.iso	en	ru
dc.publisher	Royal Society of Chemistry	ru
dc.relation.ispartofseries	New Journal of Chemistry	-
dc.subject	Alkyne derivative	ru
dc.subject	Organotin compound	ru
dc.title	Tetraalkynylstannanes in the stille cross coupling reaction: a new effective approach to arylalkynes	ru
dc.type	Статья	ru
vkr.amount	Pages 2910-2918	ru
vkr.inst	Институт математики и естественных наук	-
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