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Reaction of isocyanates with schiff bases
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| 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.