A facile stereospecific synthesis of α-hydrazino esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Inhibition of cytoplasmic aspartate aminotransferase from porcine heart by R and S isomers of aminooxysuccinate and hydrazinosuccinate.
2. Analogs of diaminopimelic acid as inhibitors of meso-diaminopimelate dehydrogenase and LL-diaminopimelate epimerase.
3. Practical synthesis of optically active α-hydrazino acids from α-amino acids
4. Antibacterial Activity and Uptake into Escherichia coli of Backbone-modified Analogues of Small Peptides
5. Design and synthesis of a CD4 beta-turn mimetic that inhibits human immunodeficiency virus envelope glycoprotein gp120 binding and infection of human lymphocytes.
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1. Stable radical cation salt initiated N–H insertion and related proton-transfer-delay three-component reaction;Tetrahedron Letters;2016-05
2. Peptidomimetics via modifications of amino acids and peptide bonds;Chemical Society Reviews;2014
3. Combinatorial Aid for Underprivileged Scaffolds: Solution and Solid-phase Strategies for a Rapid and Efficient Access To Novel Aza-diketopiperazines (Aza-DKP);ACS Combinatorial Science;2012-04-06
4. Synthesis and Chemistry of α-Hydrazino Acids;Amino Acids, Peptides and Proteins in Organic Chemistry;2010-12-28
5. ChemInform Abstract: A Facile Stereospecific Synthesis of α-Hydrazino Esters.;ChemInform;2010-05-20
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