Stereoselective synthesis of anti-β-amino-α-hydroxy acid derivatives using nucleophilic epoxidation of 1-arylthio-1-nitroalkenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Asymmetric synthesis of β-amino-α-hydroxy acids via diastereoselective hydroxylation of homochiral β-amino enolates
2. Asymmetric synthesis of the taxol and taxotère C-13 side chains
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4. Chemistry and Biology of Taxol
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1. Synthesis of Amino-Acid-Based Nitroalkenes;Organics;2022-06-14
2. N-Hydroxymethyl derivatives of α-amino aldehydes used for the stereoselective syntheses of β-amino-α-hydroxy acids;Tetrahedron: Asymmetry;2014-04
3. Rhodium-catalyzed arylthiolation reaction of nitroalkanes, diethyl malonate, and 1,2-diphenylethanone with diaryl disulfides: control of disfavored equilibrium reaction;Tetrahedron Letters;2012-10
4. ChemInform Abstract: Stereoselective Synthesis of anti-β-Amino-α-hydroxy Acid Derivatives Using Nucleophilic Epoxidation of 1-Arylthio-1- nitroalkenes.;ChemInform;2010-08-05
5. Highly stereoselective epoxidation of O-protected 3-hydroxy-1-nitroalkenes;Tetrahedron;2009-10
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