Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-9649
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Main Title: A Simple Nickel Catalyst Enabling an E‐Selective Alkyne Semihydrogenation
Author(s): Thiel, Niklas Olof
Kaewmee, Benyapa
Tran Ngoc, Trung
Teichert, Johannes F.
Type: Article
Language Code: en
Abstract: Stereoselective alkyne semihydrogenations are attractive approaches to alkenes, which are key building blocks for synthesis. With regards to the most atom economic reducing agent dihydrogen (H 2 ), only few catalysts for the challenging E ‐selective alkyne semihydrogenation have been disclosed, each with a unique substrate scope profile. Here, we show that a commercially available nickel catalyst facilitates the E ‐selective alkyne semihydrogenation of a wide variety of substituted internal alkynes. This results in a simple and broadly applicable overall protocol to stereoselectively access E ‐alkenes employing H 2 which could serve as a general method for synthesis.
URI: https://depositonce.tu-berlin.de/handle/11303/10754
http://dx.doi.org/10.14279/depositonce-9649
Issue Date: 6-Nov-2019
Date Available: 13-Feb-2020
DDC Class: 540 Chemie und zugeordnete Wissenschaften
660 Chemische Verfahrenstechnik
Subject(s): nickel
hydrogenation
alkyne
stereoselectivity
catalysis
Sponsor/Funder: DFG, 352364740, Diwasserstoff-vermittelte nachhaltige Bindungsknüpfungsreaktionen
TU Berlin, Open-Access-Mittel - 2019
License: https://creativecommons.org/licenses/by-nc-nd/4.0/
Journal Title: Chemistry – A European Journal
Publisher: Wiley
Publisher Place: Weinheim
Volume: 26
Issue: 7
Publisher DOI: 10.1002/chem.201903850
Page Start: 1597
Page End: 1603
EISSN: 1521-3765
ISSN: 0947-6539
Appears in Collections:FG Organische Chemie » Publications

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