A novel double ‘inverse electron-demand’ Diels-Alder reaction of azolyldienamines and tetrazines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Expected Selectivity and Unexpected Isomerization in the Inverse Diels-Alder Reaction of Azolyl Dienes
2. Synthesis of Azinylvinylpyridazines: A General Note on the Isomerization of Hetaryldienamines
3. PREPARATION AND DIELS-ALDER REACTION OF A REACTIVE, ELECTRON-DEFICIENT HETEROCYCLIC AZADIENE: DIMETHYL 1,2,4,5-TETRAZINE-3,6-DICARBOXYLATE. 1,2-DIAZINE (DIMETHYL 4-PHENYL-1,2-DIAZINE-3,6-DICARBOXYLATE) AND PYRROLE (DIMETHYL 3-PHENYLPYRROLE-2,5-DICARBOXYLATE) INTRODUCTION
4. Tandem ‘inverse electron-demand’ Diels-Alder reactions of dienamines with a 1,2,4,5-tetrazine. A new azo-bridged ring system
5. Pericyclic Domino reactions with 3,6-Bis(trifluoromethyl)-1,2,4,5-tetrazine: A convenient entry into azo cage compounds
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1. External electric field induced conformational change and improved stability for series of energetic pentazole anion salts: A theoretical study;Chemical Physics Letters;2021-09
2. Synthesis of α-(Trifluoromethyl)pyridazine Derivatives;European Journal of Organic Chemistry;2018-02-14
3. Indium(III) chloride/silica gel catalyzed synthesis of pyrazolo[3,4- b ]pyrrolo[3,4- d ]pyridines;Tetrahedron;2015-11
4. ChemInform Abstract: A Novel Double “Inverse Electron-Demand” Diels-Alder Reaction of Azolyldienamines and Tetrazines.;ChemInform;2010-06-12
5. Synthesis of 3,6-Divinyl-1,2,4,5-Tetrazine, the First Member of the Elusive Vinyltetrazine Family;Synlett;2009-02-16
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