Yayın:
A new Synthesis of n-substituted-1,2,3,4-tetrahydro-4-phenylisoquinolin-3-ones

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dc.contributor.buuauthorCoşkun, Necdet
dc.contributor.buuauthorSümengen, Doğan
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.date.accessioned2021-07-07T06:55:33Z
dc.date.available2021-07-07T06:55:33Z
dc.date.issued1993
dc.description.abstract1,2,3,4-Tetrahydro-4-phenylisoquinolin-3-ones 3 are obtained from appropriate N,N-disubstituted phenylacetamides 1, using lead tetraacetate ( LTA ) as oxidant and Lewis or proton acids as cyclizing agents. The methods for this conversion could be one stage ( method B or C ), or two stages ( method A ). The latter method was particularly developed to explain the mechanism of the reaction.
dc.identifier.citationCoşkun, N. ve Sümengen, D. (1993). ''A New Synthesis of N-Substituted-1,2,3,4-tetrahydro-4-phenylisoquinolin-3-ones''. Synthetic Communications, 23(10), 1393-1402.
dc.identifier.doi10.1080/00397919308011228
dc.identifier.endpage1402
dc.identifier.issn0039-7911
dc.identifier.issue10
dc.identifier.scopus2-s2.0-0027158709
dc.identifier.startpage1393
dc.identifier.urihttps://doi.org/10.1080/00397919308011228
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/00397919308011228
dc.identifier.urihttp://hdl.handle.net/11452/21136
dc.identifier.volume23
dc.identifier.wosA1993LB85400007
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherMarcel Dekker Inc
dc.relation.journalSynthetic Communications
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChemistry
dc.subject4-Aryl
dc.subjectTetrahydroisoquinolines
dc.subjectDisubstituted
dc.subject.wosChemistry, organic
dc.titleA new Synthesis of n-substituted-1,2,3,4-tetrahydro-4-phenylisoquinolin-3-ones
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.atWOS
local.indexed.atScopus

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