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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Zobova N. | |
dc.contributor.author | Andronova I. | |
dc.date.accessioned | 2018-09-14T20:29:25Z | |
dc.date.available | 2018-09-14T20:29:25Z | |
dc.date.issued | 1974 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132517 | |
dc.description.abstract | 1. The trifluoroacetyl and trichloroacetyl isocyanates react with allyl vinyl and vinyl phenyl ethers to give linear adducts of general formula R1CONHCOCH=CHOR2. Benzoyl isocyanate reacts in a similar manner with allyl vinyl ether. 2. The trifluoroacetyl and trichloroacetyl isocyanates react with p-tolyl vinyl sulfide and p-bromophenyl vinyl sulfide, while benzoyl isocyanate reacts with phenyl vinyl ether, to give the corresponding substituted dihydro -1,3 -oxazin-4-ones. 3. An NMR study of the reactions of the geometric isomers of butenyl ethyl ether with trichloroacetyl isocyanate confirmed that fact that the formation of the linear isomers proceeds via intermediate 4- and 6-membered cyclic compounds. © 1975 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Reaction of acylisocyanates with unsaturated ethers | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 7 | |
dc.relation.ispartofseries-volume | 23 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1484 | |
dc.source.id | SCOPUS05685230-1974-23-7-SID34250425956 |