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dc.creatorMihailovic, ML
dc.creatorGojkovic, S
dc.creatorMilosavljevic, S
dc.creatorKonstantinovic, S
dc.date.accessioned2018-11-22T00:02:39Z
dc.date.available2018-11-22T00:02:39Z
dc.date.issued1999
dc.identifier.issn0376-4699
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/412
dc.description.abstractThe 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.publisherNatl Inst Science Communication, New Delhi
dc.rightsrestrictedAccess
dc.sourceIndian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
dc.titleRing closure reaction of 4-tert-butyl-4-penten-1-ol with electrophilic reagentsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМихаиловиц, МЛ; Гојковиц, С; Константиновиц, С; Милосављевиц, С;
dc.citation.volume38
dc.citation.issue1
dc.citation.spage101
dc.citation.epage105
dc.identifier.wos000079830200021
dc.citation.other38(1): 101-105
dc.citation.rankM23
dc.identifier.scopus2-s2.0-0033030680
dc.identifier.rcubKon_1386


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