Synthesis of trisubstituted olefins via nickel-catalyzed decarboxylative hydroalkylation of internal alkynes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference48 articles.
1. Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure (Z)-Olefins in Polyfunctionalized Bioactive Molecules?
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4. The Preparation of Higher cis and trans Olefins1
5. Ni-catalyzed regioselective three-component coupling of alkyl halides, arylalkynes, or enynes with R–M (M = MgX′, ZnX′)
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1. Regio‐ and enantioselective nickel-alkyl catalyzed hydroalkylation of alkynes;Nature Communications;2024-08-02
2. Silanes as a versatile hydride source for Ni–H catalysis: a promising tool for π-hydro functionalization;Organic Chemistry Frontiers;2024
3. Photoredox‐ and Nickel‐Catalyzed Hydroalkylation of Alkynes with 4‐Alkyl‐1,4‐dihydropyridines: Ligand‐Controlled Regioselectivity;Chemistry – A European Journal;2022-05-13
4. Streamlined Alkylation via Nickel-Hydride-Catalyzed Hydrocarbonation of Alkenes;Journal of the American Chemical Society;2022-04-12
5. Synthesis of Tri-Substituted Olefin Derivatives from 1-Alkene-1,2-Diboronic Esters via Sequential Suzuki-Suzuki Coupling Reaction and Their Biological Activity;Polycyclic Aromatic Compounds;2021-10-18
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