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Rhodium-catalysed nucleophilic ring opening reaction of 1-and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines

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dc.contributor.author Kelebekli, Latif
dc.date.accessioned 2022-09-05T11:46:35Z
dc.date.available 2022-09-05T11:46:35Z
dc.date.issued 2013
dc.identifier.uri http://doi.org/10.3184/174751913X13663103976700
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3153
dc.description.abstract 2-Ethoxy-3- and 5-chloropyridines were obtained from 2,3- and 2,5-dichloropyridine. Reaction of 2,3- and 2,5-dichlo-ropyridines with tBuLi in the presence of furan gave 1- and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines. The rhodium-catalysed ring-opening reaction of 1- and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines with 2-bromophenol furnished the isomer 7-(2-bromophenoxy)-1-ethoxy-7,8-dihydroisoquinolin-8-ol, 6-(2-bromophenoxy)-1-ethoxy-5,6-dihydroisoquinolin-5-ol and 7-(2-bromophenoxy)-3-ethoxy-7,8-dihydroisoquinolin-8-ol, 6-(2-bromophenoxy)-3-ethoxy-5,6-dihydroisoquinolin-5-ol respectively. en_US
dc.language.iso eng en_US
dc.publisher SAGE PUBLICATIONS LTD1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND en_US
dc.relation.isversionof 10.3184/174751913X13663103976700 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject oxabicyclic alkenes, isoquinoline, regioselectivity, ring-opening, rhodium catalysis en_US
dc.title Rhodium-catalysed nucleophilic ring opening reaction of 1-and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines en_US
dc.type article en_US
dc.relation.journal SAGE PUBLICATIONS LTD1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0002-6242-2589 en_US
dc.identifier.volume 5 en_US
dc.identifier.issue 304 en_US
dc.identifier.startpage 308 en_US


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