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Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents
dc.creator | Mihailović, ML | |
dc.creator | Gojkovic, S | |
dc.creator | Milosavljevic, S | |
dc.creator | Konstantinovic, S | |
dc.date.accessioned | 2018-11-22T00:02:39Z | |
dc.date.available | 2018-11-22T00:02:39Z | |
dc.date.issued | 1999 | |
dc.identifier.issn | 0376-4699 | |
dc.identifier.uri | https://cherry.chem.bg.ac.rs/handle/123456789/412 | |
dc.description.abstract | The reaction of 4-tert-butyl-4-penten-1-ol 3 with some electrophilic reagents (such as mineral acids, mercuric acetate, peracids) has been investigated. It is found that in the acid (H2SO4) catalysed reaction of 3, the products of 1,2-methyl rearrangement are produced. The oxymercuration/demercuration reaction of 3 and its reaction with meta-chloroperbenzoic acid afford in high yields exclusively Markovnikov-type products. | en |
dc.publisher | Natl Inst Science Communication, New Delhi | |
dc.rights | restrictedAccess | |
dc.source | Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry | |
dc.title | Ring closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagents | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Михаиловиц, МЛ; Гојковиц, С; Константиновиц, С; Милосављевиц, С; | |
dc.citation.volume | 38 | |
dc.citation.issue | 1 | |
dc.citation.spage | 101 | |
dc.citation.epage | 105 | |
dc.identifier.wos | 000079830200021 | |
dc.citation.other | 38(1): 101-105 | |
dc.citation.rank | M23 | |
dc.type.version | publishedVersion | en |
dc.identifier.scopus | 2-s2.0-0033030680 | |
dc.identifier.rcub | https://hdl.handle.net/21.15107/rcub_cherry_412 |
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