Electronically Mediated Selectivity in Ring Opening of 1-Azirines. The 3-Z Mode: Convenient Route to 2-Aza-1,3-dienes
Author:
Affiliation:
1. Instituto de Química, Universidade Estadual de Campinas, C.P. 6154, Campinas, São Paulo 13.083-970, Brazil
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo980198u
Reference9 articles.
1. Electronically Mediated Selectivity in Ring Opening of 1-Azirines. The 3-X Mode: Convenient Route to 3-Oxazolines
2. Reaction of a 1-azirine-3-methylacrylate and derivatives with diphenylketene. A convenient route to 5-pyrrolin-2-ones
3. 2-aza-1,3-dienes: Methods of synthesis and stereochemical studies
4. Electronically Neutral 2-Aza-1,3-dienes: Are They Useful Intermediates in Organic Synthesis?
5. Synthesis and Reactivity of Electron-Poor 2-Azadienes. [4 + 2] Cycloaddition Reactions with Alkenes and Enamines
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1. Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study;Molecules;2023-05-24
2. 2-Azadienes as Enamine Umpolung Synthons for the Preparation of Chiral Amines;Synlett;2019-03-26
3. Copper-mediated electrophilic imination of alkenylzirconocenes with O-benzoyl ketoximes and aldoximes;Chemical Communications;2013
4. ChemInform Abstract: Electronically Mediated Selectivity in Ring Opening of 1-Azirines. The 3-Z Mode: Convenient Route to 2-Aza-1,3-dienes.;ChemInform;2010-06-15
5. Oxidative Conversion of Imines into 2-Azadienes;Synlett;2010-01-07
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