Diastereoselective synthesis of the key lactone intermediate for the preparation of hydroxyethylene dipeptide isosteres
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Inhibitors of HIV-1 Protease
2. Stereocontrolled addition of propionate homoenolate equivalents to chiral α-amino aldehydes
3. A short, stereoselective synthesis of the lactone precursor to 2R,4S,5S hydroxyethylene dipeptide isosteres
4. Addition of Allylic Metals to α-Aminoaldehydes. Application to the Synthesis of Statine, Ketomethylene and Hydroxyethylene Dipeptide Isosteres
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1. High-performance liquid chromatographic enantioseparation of isopulegol-based ß-amino lactone and ß-amino amide analogs on polysaccharide-based chiral stationary phases focusing on the change of the enantiomer elution order;Journal of Chromatography A;2020-06
2. Synthesis and Transformation of (-)-Isopulegol-Based Chiral β-Aminolactones and β-Aminoamides;International Journal of Molecular Sciences;2018-11-08
3. A silver-promoted solid-phase guanidylation process enables the first total synthesis of stictamide A;RSC Advances;2015
4. ChemInform Abstract: Diastereoselective Synthesis of the Key Lactone Intermediate (VI) for the Preparation of Hydroxyethylene Dipeptide Isosteres.;ChemInform;2010-08-19
5. An efficient asymmetric synthesis of enigmols (1-deoxy-5-hydroxysphingoid bases), an important class of bioactive lipid modulators;Arkivoc;2010-08-03
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