A new reaction system for efficient electrochemical oxidation of N-methoxycarbonyl-2,2,2-trifluoroethylamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
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2. Electroorganic chemistry. 46. A new carbon-carbon bond forming reaction at the .alpha.-position of amines utilizing anodic oxidation as a key step
3. Electrolytic reactions of fluoro organic compounds. 7. Anodic methoxylation and acetoxylation of 2,2,2-trifluoroethyl sulfides. Preparation of highly useful trifluoromethylated building blocks
4. A new approach to the chiral synthesis of the 1-.beta.-methylcarbapenem key precursor using an achiral ketone Sn(II) enolate
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1. Facile Synthesis of α‐ exo ‐Methylene Ketones from α,α‐Disubstituted Allyl Alcohols by Electrochemical Oxidative Migration;ChemElectroChem;2019-03-13
2. ChemInform Abstract: A New Reaction System for Efficient Electrochemical Oxidation of N- Methoxycarbonyl-2,2,2-trifluoroethylamines.;ChemInform;2010-08-19
3. Modern Strategies in Electroorganic Synthesis;Chemical Reviews;2008-06-20
4. Convenient enantioselective synthesis of β-trifluoromethyl-β-aminoketones by organocatalytic asymmetric Mannich reaction of aryl trifluoromethyl ketimines with acetone;Tetrahedron: Asymmetry;2008-04
5. Hydrogen Bonding in Organofluorine Compounds;Organofluorine Chemistry;2007-11-12
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