Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3153
Title: Rhodium-catalysed nucleophilic ring opening reaction of 1-and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines
Authors: Kelebekli, Latif
Ordu Üniversitesi
0000-0002-6242-2589
Keywords: oxabicyclic alkenes, isoquinoline, regioselectivity, ring-opening, rhodium catalysis
Issue Date: 2013
Publisher: SAGE PUBLICATIONS LTD1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
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.
URI: http://doi.org/10.3184/174751913X13663103976700
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3153
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