Gold-catalyzed oxidation of propargylic ethers with internal C–C triple bonds: Impressive regioselectivity enabled by inductive effect
Author:
Funder
NIGMS
NIH
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference72 articles.
1. For our own work, see:
2. Gold-Catalyzed One-Step Practical Synthesis of Oxetan-3-ones from Readily Available Propargylic Alcohols
3. Alkynes as Equivalents of α-Diazo Ketones in Generating α-Oxo Metal Carbenes: A Gold-Catalyzed Expedient Synthesis of Dihydrofuran-3-ones
4. An Efficient [2 + 2 + 1] Synthesis of 2,5-Disubstituted Oxazoles via Gold-Catalyzed Intermolecular Alkyne Oxidation
5. A Flexible and Stereoselective Synthesis of Azetidin-3-ones through Gold-Catalyzed Intermolecular Oxidation of Alkynes
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2. Regio- and stereoselective oxidative conversion of alkynes to sulfenylated α,β-unsaturated carbonyls;Organic Chemistry Frontiers;2023
3. Kontrolle der Selektivität in Shuttle‐Heterodifunktionalisierungen: Elektrochemische Transfer‐Halothiolierung von Alkinen;Angewandte Chemie;2022-12-13
4. Controlling Selectivity in Shuttle Hetero‐difunctionalization Reactions: Electrochemical Transfer Halo‐thiolation of Alkynes;Angewandte Chemie International Edition;2022-12-13
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