Search Results

Now showing 1 - 2 of 2

Citation - WoS: 21
Citation - Scopus: 21
Palladium-Catalyzed Alkoxycarbonylation of Conjugated Enyne Oxiranes: a Diastereoselective Method for the Synthesis of 7-Hydroxy
(American Chemical Society, 2015) Kuş, Melih; Artok, Levent; Aygün, Muhittin
Palladium-catalyzed alkoxycarbonylative 1,5-substitution of conjugated enyne oxiranes provides a diastereoselective route to (E)-configured 7-hydroxy-2,3,5-trienoates. The reactions proceeded in a highly stereoselective manner, possibly through sequential formation of π-allylpalladium and σ-vinylallenyl palladium complexes. The major diastereomeric form of the product is determined by the configuration of the alkenyl moiety of the substrate.
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; Artok, Levent
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.

Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection