dc.contributor.author |
Veremeichik Y. |
|
dc.contributor.author |
Shurpik D. |
|
dc.contributor.author |
Lodochnikova O. |
|
dc.contributor.author |
Plemenkov V. |
|
dc.date.accessioned |
2018-09-19T21:02:21Z |
|
dc.date.available |
2018-09-19T21:02:21Z |
|
dc.date.issued |
2016 |
|
dc.identifier.issn |
1070-4280 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/143515 |
|
dc.description.abstract |
© Pleiades Publishing, Ltd., 2016.N-Sulfinyl-3-(trifluoromethyl)aniline reacted with bicyclo[2.2.1]hept-2-ene and bicyclo[2.2.1]hepta-2,5-diene to give the corresponding Diels‒Alder adducts which were oxidized to 8-trifluoromethyl2,3,4,4a,6,10b-hexahydro-5λ6-1,4-methanodibenzo[c,e][1,2]thiazine-5,5(1H)-diones. The cycloaddition occurred predominantly with participation of the S=N–C1=C6 fragment of N-sulfinyl-3-(trifluoromethyl)aniline and exclusively at the endo side of bicyclo[2.2.1]heptenes. |
|
dc.relation.ispartofseries |
Russian Journal of Organic Chemistry |
|
dc.title |
Synthesis of cyclic sulfonamides by reaction of N-Sulfinyl-3-(trifluoromethyl)aniline with Norbornenes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
1 |
|
dc.relation.ispartofseries-volume |
52 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
92 |
|
dc.source.id |
SCOPUS10704280-2016-52-1-SID85007545285 |
|