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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 |