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Please use this identifier to cite or link to this item: http://digitalrepository.fccollege.edu.pk/handle/123456789/1284
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dc.contributor.authorMonticelli, Serena-
dc.contributor.authorCastoldi, Laura-
dc.contributor.authorTouqeer, Saad-
dc.contributor.authorMiele, Margherita-
dc.contributor.authorUrban, Ernst-
dc.contributor.authorPace, Vittorio-
dc.date.accessioned2021-04-29T11:52:30Z-
dc.date.available2021-04-29T11:52:30Z-
dc.date.issued2018-06-07-
dc.identifier.citationMonticelli, S., Castoldi, L., Touqeer, S. et al. Recent advances in the synthesis and reactivity of spiro-epoxyoxindoles. Chem Heterocycl Comp 54, 389–393 (2018). https://doi.org/10.1007/s10593-018-2280-4en_US
dc.identifier.otherhttps://doi.org/10.1007/s10593-018-2280-4-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1284-
dc.descriptionhttps://link.springer.com/article/10.1007/s10593-018-2280-4#citeasen_US
dc.description.abstractSpiro-epoxyoxindoles containing an unsubstituted methylene fragment in the oxirane ring are excellent building blocks in organic syn thesis due to the high reactivity conferred by the three-membered oxygenated cycle. In this minireview, a concise survey of the methods of their synthesis and examples of reactivity with carbon and nitrogen nucleophiles is presented, with a particular focus on the stereo chemical aspects. The review covers the literature for the last twenty years.en_US
dc.language.isoenen_US
dc.publisherspringer linken_US
dc.relation.ispartofseriesChem Heterocycl Comp 54, 389–393 (2018).;-
dc.subjectnucleophilic addition.en_US
dc.subjectepoxides,en_US
dc.subjectisatins,en_US
dc.subjectspiro compounds,en_US
dc.subjectFriedel–Crafts reaction,en_US
dc.titleRecent advances in the synthesis and reactivity of spiro-epoxyoxindolesen_US
dc.typeArticleen_US
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