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 |
|