Azomethine ylids from diethyl aminomalonate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
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2. Pyrrolidine ring formation by a new base-promoted 1,3-dipolar cycloaddition of N-(phenylthiomethyl) amino acid esters
3. Trimethylamine N-oxide as a precursor of azomethine ylides
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1. New functionalized pyrrolidines;Russian Journal of Organic Chemistry;2017-03
2. Paraformaldehyde;Encyclopedia of Reagents for Organic Synthesis;2008-03-14
3. Diethyl aminomalonate;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
4. Synthesis of Highly Functionalized Pyrrolidines via a Mild One-Pot, Three-Component 1,3-Dipolar Cycloaddition Process;The Journal of Organic Chemistry;2005-11-22
5. A stereodivergent cascade imine→azomethine ylide→1,3-dipolar cycloadditive approach to α-chiral pyrrolidines;Tetrahedron Letters;2005-08
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