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Citation - WoS: 7
Citation - Scopus: 7
Rhodium-Catalysed Alkoxycarbonylative Cyclisation Reactions of 1,6-Enynes
(John Wiley and Sons Inc., 2011) Ziyanak, Fırat; Kuş, Melih; Kuş, Melih; Artok, Levent; Ziyanak, Fırat; 04.01. Department of Chemistry; 04. Faculty of Science; 01. Izmir Institute of Technology
The rhodium-catalysed carbonylation of 1,6-enynes possessing an electron-deficient alkenyl moiety in an alcohol reagent in the presence of a rhodium complex proceeded stereo- and chemoselectively to afford exocyclic α,β-enoates.
Citation - WoS: 15
Citation - Scopus: 14
Rhodium 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; Artok, Levent; Türkmen, Gülşah; Aksın Artok, Özge; Kuş, Melih; 04.01. Department of Chemistry; 04. Faculty of Science; 01. Izmir Institute of Technology
Unsymmetric 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.

Chemistry / Kimya