Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/3287
Title: The synthesis of furanones via rhodium-catalyzed carbonylative addition reactions of arylboronic acids to alkynes
Authors: Dege, Fatma Nurcan
Advisors: Artok, Levent
Publisher: Izmir Institute of Technology
Abstract: This study reveals that 5-Aryl-2(5H)-furanones can be synthesized by rhodiumcatalyzed reaction of arylboronic acids with internal alkynes under a CO atmosphere.In this thesis, relatively mild and simple method for synthesis of 2(5H)-furanones was developed. Our method was found to be applicable for various arylboronic acids and alkynes.The methodology of this study is well applicable for ortho-, para- and metasubstituted phenylboronic acids. But slightly higher yields were obtained with parasubstituted phenylboronic acids than ortho- or meta- substituted ones.It was found that when an asymmetric alkyne is used under the optimized conditions, aroylation occurs more on the electron deficient acetylenic carbon as compared with electron rich acetylene when aroylrhodium(I) species undergoes 1,2-addition to the carbon-carbon triple bond in the reaction. That affects the ratio of isomeric yields of furanones which were produced in the reactions of asymmetric alkynes with phenylboronic acid.2(5H)-Furanones that we synthesized can be used in many areas such as food manufacturing, perfume and medicinal industries.
Description: Thesis (Master)--İzmir Institute of Technology, Chemistry, İzmir, 2008
Includes bibliographical references (leaves: 65-73)
Text in English; Abstract: Turkish and English
xii, 242 leaves
URI: http://hdl.handle.net/11147/3287
Appears in Collections:Master Degree / Yüksek Lisans Tezleri

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