X=Y-ZH Compounds as potential 1,3-dipoles. Part 30. Cycloaddition of arylidene imines of α-amino esters to acetylenic dipolarophiles and pyrrole forming rearrangements
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds
2. XY–ZH systems as potential 1,3-dipoles. Part 1. Background and scope
3. XY–ZH systems as potential 1,3-dipoles. Part 7. Stereochemistry of the cycloaddition of imines of α-amino acid esters to fumarate and maleate esters
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2. Short and efficient synthesis of 2H-pyrroles from 7-oxanorbornadiene derivatives;Tetrahedron;2011-01
3. Stereoselective 1,3-Dipolar Cycloaddition of a Maleate Derivative with Azomethine Ylides Derived from α-Amino Esters: Synthesis of 3-Pyrrolines;Synlett;2007-05-08
4. Reaction of functionalized azomethine ylides with acetylenic dipolarophiles: the facile synthesis of functionalized 2H- and 1H-pyrroles;Tetrahedron Letters;2007-02
5. An Unusual and Stereoselective Michael Addition of αAmino Ester-Derived N-Lithiated Azomethine Ylides;Letters in Organic Chemistry;2006-09-01
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