Palladium-Catalysed Reactions of Conjugated Enyne Oxiranes With Organoborons: a Diastereoselective Method of the Synthesis of 2,4,5-Trienol Derivatives
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Date
2017
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Open Access Color
BRONZE
Green Open Access
Yes
OpenAIRE Downloads
2
OpenAIRE Views
2
Publicly Funded
No
BIP! Indicators
Impulse
Top 10%
Influence
Average
Popularity
Top 10%
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.
Description
Keywords
Enyne oxirane, Organoboron, Vinylallene, 2,4,5-Trienol, Allene derivative, Allene derivative, Allene, Enyne oxirane, 2,4,5-Trienol, Organoboron, Vinylallene
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
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
WoS Q
Q2
Scopus Q
Q3
OpenCitations Citation Count
6
Source
Tetrahedron
Volume
74
Issue
27
Start Page
3652
End Page
3662
PlumX Metrics
Citations
CrossRef : 7
Scopus : 6
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Mendeley Readers : 5
SCOPUS™ Citations
6
checked on Apr 27, 2026
Web of Science™ Citations
6
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Page Views
1122
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Downloads
565
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