A regiospecific synthesis of 2-azaanthraquinon-3-ones via a hetero Diels-Alder reaction with bromonaphthoquinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
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3. Regiochimie De La Cycloaddition Des 2-Azadienes Disilyles Avec Les Derives De La 1,4-Naphtoquinone
4. Regiochemical control in the Diels-Alder reactions of substituted naphthoquinones. Model studies on a regiospecific approach to adriamycinone
5. Diels-Alder cycloaddition of juglone derivatives: elucidation of factors influencing regiochemical control
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1. A survey of synthetic routes towards 2-azaanthraquinones;Tetrahedron;2011-12
2. ChemInform Abstract: A Regiospecific Synthesis of 2-Azaanthraquinon-3-ones via a Hetero- Diels-Alder Reaction with Bromonaphthoquinones.;ChemInform;2010-08-20
3. Diels–Alder cycloaddition of 2-azadienes to methyl 2-(2,6-dichlorophenyl)-2H-azirine-3-carboxylate in the synthesis of methyl 4-oxo-1,3-diazabicyclo[4.1.0]heptane-6-carboxylates;Tetrahedron;2004-07
4. Regiocontrolled [3+2] quinone-nitrile oxide entry to type II polyketide building blocks;Tetrahedron Letters;2003-12
5. Recent advances in synthetic applications of azadienes;Tetrahedron;2002-01
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