Stereocontrolled synthesis of 3,5-dialkyl-4-amino pyrrolidin-2-ones from β-lactams as chiral templates.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference35 articles.
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4. Highly diastereoselective Michael addition of lithiated camphor imines of glycine esters to .alpha.,.beta.-unsaturated esters. Synthesis of optically pure 5-oxo-2,4-pyrrolidinedicarboxylates of unnatural stereochemistry
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1. Inverconversion of Nitriles, Carboxylic Acids, and Derivatives;Comprehensive Organic Transformations;2018-02-28
2. Gold-catalyzed preparation of annelated 2-azetidinones via divergent heterocyclization of enyne-tethered oxazolidines;Organic Chemistry Frontiers;2018
3. Synthesis of Five-Membered Heterocycles Through β-Lactam Ring-Expansion Reaction;Beta-Lactams;2017
4. Copper catalyzed oxidative cross-coupling of aromatic amines with 2-pyrrolidinone: a facile synthesis of N-aryl-γ-amino-γ-lactams;Tetrahedron;2014-09
5. ChemInform Abstract: Stereocontrolled Synthesis of 3,5-Dialkyl-4-amino Pyrrolidin-2-ones from β-Lactams as Chiral Templates.;ChemInform;2010-08-21
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