Oligomeric iodosylbenzene sulfate: a convenient hypervalent iodine reagent for oxidation of organic sulfides and alkenes; Synthesis; № 15
| Parent link: | Synthesis № 15.— 2009.— [P. 2505-2508] |
|---|---|
| Övriga upphovsmän: | Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Yusubova R. Ya. Roza Yavidovna, Funk T. V. Tatyana V., Chi Ki-Whan, Zhdankin V. V. Viktor Vladimirovich |
| Sammanfattning: | Title screen Исследованы окисления алкенов посредством реактива (PhIO)[3]SO[3], генерированного in situ из (диацетоксииод)бензола и бисульфата натрия: PhC(R)=CH[2]+PhI(OAc)[2], NaHSO[4]·H[2]O, перемалывание (0,5-1 минута, ~20°)→PhCH[2]COR (R=Ph, H, Me), выход 83-97%; (~#I_%)+PhI(OAc)[2], NaHSO[4]·H[2]O, перемалывание (0,5-1 минута, ~20°)→c-C[5]H[9]COR (R=H, Me), выход 39-45%. Режим доступа: по договору с организацией-держателем ресурса |
| Språk: | engelska |
| Publicerad: |
2009
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| Ämnen: | |
| Länkar: | http://dx.doi.org/10.1055/s-0029-1216870 |
| Materialtyp: | Elektronisk Bokavsnitt |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=649328 |
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Liknande verk
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Preparation and structure of oligomeric iodosylbenzene sulfate (PhIO)[3]·SO[3]: stable and water-soluble analog of iodosylbenzene; European Journal of Organic Chemistry; Vol. 2007, iss. 27
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m-Iodosylbenzoic acid, a tagged hypervalent iodine reagent for the iodo-functionalization of alkenes and alkynes; Tetrahedron Letters; Vol. 49, iss. 9
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