Studies on the regioselectivity of intermolecular diels-alder cycloadditions of 1-methylpyrano[3,4-b]indol-3-one and the N-acetylated derivative
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Indolo‐α‐pyrone und Indolo‐α‐pyridone
2. Diels–Alder reactivity of pyrano[3,4-b]indol-3-ones, stable, synthetic equivalents of indole-2,3-quinodimethanes
3. A concise synthesis of the antitumour alkaloid ellipticine
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1. Diels-Alder Cycloaddition;Indole Ring Synthesis;2016-06-17
2. Regioselective Synthesis of Elusive 4,9-Dihydro-1H-Carbazoles by Gold-Catalyzed Cycloisomerization of 3-Allenylmethylindoles;The Journal of Organic Chemistry;2013-09-20
3. 3-Cyanomethyl-2-vinylindoles as thermal indole-2,3-quinodimethane equivalents: synthesis of functionalized 1,2,3,4-tetrahydrocarbazoles;Tetrahedron Letters;2002-10
4. Synthesis and resolution of a C2-symmetrical indolo-2,3-quinodimethane dimer;Tetrahedron Letters;1999-10
5. Diels - Alder Reactions of 1,1-Bis(methylthio)ethene with Pyran-2-ones.;Australian Journal of Chemistry;1998
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