A convenient synthesis of tetrazole, precursors of α-dialkylated α-amino acids, by reaction of trimethylsilyl azide with α-dialkylated β-ketoesters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds
2. Stereoselective synthesis of quaternary α-amino acids. Part 2: Cyclic compounds
3. Asymmetric Synthesis of α,α-Disubstituted α-Amino Acids Using (S,S)-Cyclohexane-1,2-diol as a Chiral Auxiliary
4. Asymmetric synthesis of α-alkylated α-amino acids via Schmidt rearrangement of α, α-bisalkylated β-keto esters
5. Asymmetric synthesis of α-alkylated α-amino acids: azocane-2-carboxylic acids
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1. One‐Pot Synthesis of β‐Ketoesters from Aryl Methyl Ketone via Ketene Dithioacetal;ChemistrySelect;2023-10-11
2. Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate;Tetrahedron Letters;2019-05
3. Thiourea catalysed reduction of α-keto substituted acrylate compounds using Hantzsch ester as a reducing agent in water;RSC Advances;2017
4. Synthesis and biological properties of amino acids and peptides containing a tetrazolyl moiety;Russian Chemical Reviews;2015-09-30
5. A review of syntheses of 1,5-disubstituted tetrazole derivatives;Molecular Diversity;2014-10-02
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