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Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates

dc.contributor.buuauthorNecdet, Coşkun
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.date.accessioned2021-07-01T06:26:34Z
dc.date.available2021-07-01T06:26:34Z
dc.date.issued1997-03-31
dc.description.abstractDelta(3)-imidazoline 3-oxides 1 underwent regio and diastereoselective cycloaddition with aryl isocyanates 2 to give 5,6,7.7a-tetrahydroimidazo[1.5-(b) over bar][1.2.4]oxadiazol-2(<1(H)over bar>)-ones 3 in excellent yields. Thermally and chemically induced retro cycloaddition of compounds 3 was demonstrated.
dc.identifier.citationCoşkun, N. (1997). "Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates". Tetrahedron Letters, 38(13), 2299-2302.
dc.identifier.doi10.1016/S0040-4039(97)00297-9
dc.identifier.endpage2302
dc.identifier.issn0040-4039
dc.identifier.issue13
dc.identifier.scopus2-s2.0-0031592590
dc.identifier.startpage2299
dc.identifier.urihttps://doi.org/10.1016/S0040-4039(97)00297-9
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403997002979
dc.identifier.urihttp://hdl.handle.net/11452/20950
dc.identifier.volume38
dc.identifier.wosA1997WQ04800030
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherPergamon-Elsevier Science
dc.relation.journalTetrahedron Letters
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChemistry
dc.subjectN-oxides
dc.subject.wosChemistry, organic
dc.titleRegio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates
dc.typeArticle
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.atWOS
local.indexed.atScopus

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