Reactivite dipolaire-1,3 d'imines derivees d'α-amino-acides.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. 1,3-Dipolar cycloaddition reactions of imines of α-amino-acid esters: X-ray crystal and molecular structure of methyl 4-(2-furyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo[3.3.0]octane-2-carboxylate
2. 3-Cyano-3-methoxycarbonyl-2,4,4,5-tetraphenylpyrrolidine as a precursor of benzylidenammonium benzylide
3. Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalent
4. Cycloaddition dipolaire 1,3 sur des composes a liaison ethylenique activee—XVII
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3. Hydroxy-assisted regio- and stereoselective synthesis of functionalized alkenes via phosphine-catalyzed β′-umpolung addition of o-hydroxy aromatic aldimines to allenoates;Organic Chemistry Frontiers;2018
4. Hydroxy-Assisted Regio- and Stereoselective Synthesis of Functionalized 4-Methylenepyrrolidine Derivatives via Phosphine-Catalyzed [3 + 2] Cycloaddition of Allenoates with o-Hydroxyaryl Azomethine Ylides;The Journal of Organic Chemistry;2017-11-10
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