Приказ основних података о документу
Oxidative hydrolysis and acid-catalyzed rearrangement of steroidal isoxazolidines
dc.creator | Rajković, Milica M. | |
dc.creator | Lorenc, Ljubinka | |
dc.creator | Petrović, Ivanka | |
dc.creator | Milovanović, Aleksandar Ž. | |
dc.creator | Mihailović, Milhailo Lj. | |
dc.date.accessioned | 2021-03-16T11:38:42Z | |
dc.date.available | 2021-03-16T11:38:42Z | |
dc.date.issued | 1991 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.issn | 1873-3581 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4362 | |
dc.description.abstract | Treatment of steroidal isoxazolidines 3a, 3b and 5b with N-methylhydroxylamine hydrochloride in boiling ethanol-pyridine (1:1) solution results in elimination of the CH3NH2fragment, affording products of oxidative hydrolysis 4a, 4b, and 6b, while acid-catalyzed reaction of isoxazolidines 2a, 3a and 5b leads to rearrangement involving the N-CH3 group with formation of the perhydro-3,1-oxazine derivatives 8a, 9a and 10b. | sr |
dc.language.iso | en | sr |
dc.publisher | Elsevier | sr |
dc.rights | restrictedAccess | sr |
dc.source | Tetrahedron Letters | sr |
dc.subject | 1-oxazines | sr |
dc.subject | acid-catalyzed rearrangement | sr |
dc.subject | oxidative hydrolysis | sr |
dc.subject | stereoidal perhydro-3 | sr |
dc.subject | steroidal isoxazolidines | sr |
dc.title | Oxidative hydrolysis and acid-catalyzed rearrangement of steroidal isoxazolidines | sr |
dc.type | article | sr |
dc.rights.license | ARR | sr |
dcterms.abstract | Петровић, Иванка; Рајковић, Милица М.; Лоренћ, Љубинка Б.; Михаиловíћ, Милхаило Љ.; Миловановић, Aлександар Ж.; | |
dc.citation.volume | 32 | |
dc.citation.issue | 51 | |
dc.citation.spage | 7605 | |
dc.citation.epage | 7608 | |
dc.identifier.doi | 10.1016/0040-4039(91)80546-I | |
dc.identifier.scopus | 2-s2.0-0026335197 | |
dc.type.version | publishedVersion | sr |