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Radical annulation methodology. 2-Vinylcyclopentane derivative formation by a 3 + 2 cycloaddition reaction
dc.creator | Saičić, Radomir | |
dc.creator | Čeković, Živorad | |
dc.date.accessioned | 2018-11-22T00:00:20Z | |
dc.date.available | 2018-11-22T00:00:20Z | |
dc.date.issued | 1990 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.uri | https://cherry.chem.bg.ac.rs/handle/123456789/21 | |
dc.description.abstract | By thermally or photolytically induced decomposition of O-acyl derivatives of N-hydroxypyridine-2-thione or other thiohydroxamic esters, in the presence of an excess of electron deficient olefins, 2-vinylcyclopentane derivatives were obtained. This sequence of addition/cyclization/elimination reaction is mediated by a phenylthio radical. © 1990. | en |
dc.rights | openAccess | |
dc.source | Tetrahedron Letters | |
dc.title | Radical annulation methodology. 2-Vinylcyclopentane derivative formation by a 3 + 2 cycloaddition reaction | en |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.volume | 31 | |
dc.citation.issue | 29 | |
dc.citation.spage | 4203 | |
dc.citation.epage | 4206 | |
dc.identifier.doi | 10.1016/S0040-4039(00)97582-8 | |
dc.citation.other | 31(29): 4203-4206 | |
dc.type.version | publishedVersion | |
dc.identifier.scopus | 2-s2.0-0025308645 | |
dc.identifier.fulltext | https://cherry.chem.bg.ac.rs/bitstream/id/9035/19.pdf |