A Simple Nickel Catalyst Enabling an E ‐Selective Alkyne Semihydrogenation-Reference-Cited by-同舟云学术

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A Simple Nickel Catalyst Enabling an E ‐Selective Alkyne Semihydrogenation

Published:2020-01-21 Issue:7 Volume:26 Page:1597-1603
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Thiel Niklas O.¹^ORCID,Kaewmee Benyapa¹,Tran Ngoc Trung¹,Teichert Johannes F.¹^ORCID

Affiliation:

1. Institut für ChemieTechnische Universität Berlin Strasse des 17. Juni 115 10623 Berlin Germany

Funder

Deutsche Forschungsgemeinschaft

Verband der Chemischen Industrie

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201903850

Reference87 articles.

1. Stereoselective Alkene Synthesis

2.

3. Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure (Z)-Olefins in Polyfunctionalized Bioactive Molecules?

4. Modern Trends in Catalyst and Process Design for Alkyne Hydrogenations

5. Homogeneous Hydrogenation of Alkynes and Dienes

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2. Bimetallic [Ge-Rh] complex catalyzed alkyne semihydrogenation: Theoretical investigations on the germanium promoted mechanism and selectivity;Molecular Catalysis;2024-05

3. The development and application of homogeneous nickel catalysts for transfer hydrogenation and related reactions;Coordination Chemistry Reviews;2024-05

4. Recent advances in the selective semi-hydrogenation of alkyne to (E)-olefins;Chemical Communications;2024

5. Nickel-catalyzed tandem conversion of paraformaldehyde : methanol to hydrogen and formate/chemo- and stereoselective hydrogenation of alkynes under neutral conditions;Catalysis Science & Technology;2024

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