Neighboring Carbonyl Group Assisted Oxyacetoxylation of Propargylic Carboxylates with Retention of Chirality under Metal Free Condition
Author:
Affiliation:
1. Department of Organic Synthesis and Process Chemistry, CSIR-IndianInstitute of Chemical Technology Hyderabad- 500007 India
Publisher
Wiley
Subject
Organic Chemistry,Catalysis
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900314
Reference87 articles.
1. For aerobic difunctionalization of terminal alkynes see:
2. Optimizing P,N-Bidentate Ligands for Oxidative Gold Catalysis: Efficient Intermolecular Trapping of α-Oxo Gold Carbenes by Carboxylic Acids
3. Synthesis of Imidazo[1,2-a]pyridines: “Water-Mediated” Hydroamination and Silver-Catalyzed Aminooxygenation
4. Gold(I)-Catalyzed Aminohalogenation of FluorinatedN′-Aryl-N-Propargyl Amidines for the Synthesis of Imidazole Derivatives under Mild Conditions
5. Direct use of dioxygen as an oxygen source: catalytic oxidative synthesis of amides
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2. Metal‐Free Oxyacetoxylation of Arylynamines and Ynamides To Construct α‐Acetoxyl Amides;European Journal of Organic Chemistry;2023-07-26
3. Selective Monoethynylation of 2‐Oxoacetamides Using Calcium Carbide as a Concise Solid Alkyne Source;Chemistry – An Asian Journal;2022-08-16
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