Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 15Citation - Scopus: 14Rhodium Catalysed Chemo- and Stereoselective Arylative and Alkenylative Cyclisation Reactions of Unsymmetric Diynes Containing a Terminal Alkyne Moiety With Organoboronic Acids(Royal Society of Chemistry, 2010) Artok, Levent; Kuş, Melih; Ürer, Bağdagül N.; Türkmen, Gülşah; Aksın Artok, ÖzgeUnsymmetric diynes possessing a terminal alkyne moiety reacted with organoboronic acids both chemo- and stereoselectively to afford arylated or alkenylated exocyclic dienes by catalysis from the [Rh(cod)OCH 3] 2 complex. The use of a polar protic solvent, e.g. CH 3OH is required for the success of the process under mild conditions. © 2010 The Royal Society of Chemistry.Article Citation - WoS: 25Citation - Scopus: 20Rhodium-Catalyzed Carbonylative Arylation of Alkynes With Arylboronic Acids: an Efficient and Straightforward Method in the Synthesis of 5-Aryl(Royal Society of Chemistry, 2006) Aksın, Özge; Dege, Nurcan; Artok, Levent; Türkmen, Hayati; Çetinkaya, Bekir5-Aryl-2(5H)-furanones can be synthesized by the Rh-catalyzed reactions of arylboronic acids with internal alkynes under a CO atmosphere.
