Reaction of isocyanates with schiff bases

dc.contributor.author	Zobova N.
dc.contributor.author	Rusanov G.
dc.contributor.author	Arbuzov B.
dc.date.accessioned	2018-09-14T20:26:30Z
dc.date.available	2018-09-14T20:26:30Z
dc.date.issued	1972
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/132481
dc.description.abstract	1. Electron-donor substituents in the p-positions of the aromatic rings in Schiff bases increase the overall addition rate of the benzoyl and trichloroacetyl isocyanates to Schiff bases and shift the reaction toward the formation of 4-membered rings, whereas electron-acceptor substituents shift the reaction toward the formation of oxidiazinone derivatives. 2. Highly polar solvents (dimethyl sulfoxide and SO2) promote the formation of hexahydro-S-triazine-dione derivatives. © 1973 Consultants Bureau.
dc.relation.ispartofseries	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title	Reaction of isocyanates with schiff bases
dc.type	Article
dc.relation.ispartofseries-issue	9
dc.relation.ispartofseries-volume	21
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1957
dc.source.id	SCOPUS05685230-1972-21-9-SID34250435479

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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.