Stable Configuration of Ester-Stabilized Azomethine Ylides. Stabilization ofanti-Form by 1,5-Dipolar Interaction and ofsyn-Form by Hydrogen Bonding
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
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1. Double 1,3-dipolar cycloaddition of N-methyl Azomethine ylide to meta-Dinitrobenzene annelated with nitrogen aromatic heterocycles;Journal of Heterocyclic Chemistry;2010-06-17
2. An expedient synthesis of diversified pyrrolizines and indolizines;Tetrahedron Letters;2004-02
3. Stereoselective pyrroline-ring formation through the cyclization of conjugated azomethine ylides at the periphery of pyrido[1,2-a]pyrimidine system;Tetrahedron;2003-06
4. The generation and reactivity of N-substituted, stabilised α,β:γ,δ-unsaturated azomethine ylides;Tetrahedron;2002-01
5. Synthesis of ferrocene substituted pyrrolidine derivatives via Et2Zn catalyzed 1,3-dipolar cycloaddition reactions of azomethine ylides;Journal of Organometallic Chemistry;2001-08
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