Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/7610
Title: Palladium-Catalysed Reactions of Conjugated Enyne Oxiranes With Organoborons: a Diastereoselective Method of the Synthesis of 2,4,5-Trienol Derivatives
Authors: Ziyanak, Fırat
Kuş, Melih
Alkan Karadeniz, Leman
Artok, Levent
Keywords: Enyne oxirane
Organoboron
Vinylallene
2,4,5-Trienol
Allene derivative
Publisher: Elsevier
Source: Ziyanak, F., Kuş, M., Alkan Karadeniz, L., and Artok, L. (2018). Palladium-catalysed reactions of conjugated enyne oxiranes with organoborons: A diastereoselective method of the synthesis of 2,4,5-trienol derivatives. Tetrahedron, 74(27), 3652-3662. doi:10.1016/j.tet.2018.05.030
Abstract: A palladium-catalysed reaction of conjugated enyne oxiranes with organoboron reagents is described. This method allows aryl-substituted vinylallenes containing a hydroxyl group on the allylic position to be synthesized, with good diastereomeric ratios, under mild conditions.
URI: https://doi.org/10.1016/j.tet.2018.05.030
https://hdl.handle.net/11147/7610
ISSN: 0040-4020
1464-5416
Appears in Collections:Chemistry / Kimya
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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