Oxidative addition of azide anion to triisopropylsilyl enol ethers: synthesis of α-azido ketones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. The asymmetric synthesis of α-amino and α-hydrazino acid derivatives via the stereoselective amination of chiral enolates with azodicarboxylate esters
2. Stereoselective amination of chiral enolates. A new approach to the asymmetric synthesis of .alpha.-hydrazino and .alpha.-amino acid derivatives
3. Stereoselective preparation of synthetic equivalents of 2-deoxy-2-amino- and 3-deoxy-3-aminotetroses from malic acid. Application to the synthesis of C18-D-ribo-phytosphingosine
4. Asymmetric electrophilic amination: synthesis of .alpha.-amino and .alpha.-hydrazino acids with high optical purity
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3. Cyclic Hypervalent Iodine Reagents for Azidation: Safer Reagents and Photoredox-Catalyzed Ring Expansion;The Journal of Organic Chemistry;2018-09-15
4. An Efficient Tertiary Azidation of 1,3-Dicarbonyl Compounds in Water Catalyzed by Tetrabutylammonium Iodide;European Journal of Organic Chemistry;2015-12-15
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