Intramolecular [4+2] cycloaddition reactions of indolylalkylpyridazines: synthesis of annulated carbazoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. „Inverse” Diels-Alder-Additionen, 4. Mitt.: π-Elektronenreiche, benzokondensierte Heteroaromaten als „inverse” Dienophile
2. The Cycloaddition of 1,2,4,5-Tetrazines with Indoles. The Formation of 5H-Pyridazino[4,5-b]indoles
3. Indole as a dienophile in inverse electron demand Diels-Alder reactions. 5H-Pyridazino[4,5-b]indoles as cycloadducts with 3,6-dicarbomethoxy-1,2,4,5-tetrazine
4. Inverse-Electron-Demand Diels-Alder Reactions of Condensed Pyridazines, 5. 1,4-Bis(trifluoromethyl)pyridazino[4,5-b]indole as an Azadiene
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