Regiochemical control in the diels alder reactions of substituted naphthoquinones: Orientational manipulation in the synthesis of anthraquinones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Regiochemical control in the Diels-Alder reactions of substituted naphthoquinones. Model studies on a regiospecific approach to adriamycinone
2. The New Syntheses of Hydroxydroserone (The Pigment of Drosera Whittakeri), Phthiocol (The Pigment of Human Tubercle Bacillus), and Naphthopurpurin; and the Studies of the related Compounds
3. Nuclear Magnetic Resonance Spectra of Substituted Naphthoquinones. Influence of Substituents on Tautomerism, Anisotropy, and Stereochemistry in the Naphthazarin System1
4. The Addition of Dienes to Halogenated and Hydroxylated Naphthoquinones
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1. The Total Synthesis of Naturally Occurring Quinones;Total Synthesis of Natural Products;2007-02-20
2. Anthraquinones;Naturally Occurring Quinones IV;1997
3. Regioselectivity of the Diels-Alder reactions of 2,5,8(1H)-quinolinetriones;Tetrahedron;1994-01
4. Total synthesis of (±)-fredericamycin A. Use of radical spirocyclization;J. Chem. Soc., Chem. Commun.;1992
5. An enantioselective synthesis of (+)-bostrycin leading to a revision of the absolute configuration of its natural antipode;Tetrahedron;1990-01
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