Inverse-electron-demand diels-alder reactions of condensed pyridazines, part 2. Synthesis of isoquinoline derivatives from pyrido[3,4-d]pyridazines.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Reactions of Tetrazines with Unsaturated Compounds. A New Synthesis of Pyridazines
2. Diels-Alder-Additionen mit „inversem” Elektronenbedarf
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1. Electronic and Steric Effects on the Mechanism of the Inverse Electron Demand Diels−Alder Reaction of 2-Aminopyrroles with 1,3,5-Triazines: Identification of Five Intermediates by 1H, 13C, 15N, and 19F NMR Spectroscopy;The Journal of Organic Chemistry;2008-11-18
2. Indole as a dienophile in inverse electron demand diels-alder and related reactions;Advances in Cycloaddition;1999
3. Enamines as Synthons in the Synthesis of Heterocycles;Advances in Heterocyclic Chemistry Volume 72;1998
4. Hetero Diels-Alder reactions in organic chemistry;Topics in Current Chemistry;1997
5. Inverse-electron-demanddiels-alder reactions of condensed pyridazines VI: Ring transformations of pyrido[2,3-d]pyridazine intog-fused quinolines;Monatshefte für Chemie - Chemical Monthly;1995-02
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