Enzymatic desymmetrization/resolution of epoxydiols derived from 1,4-naphthoquinone, 5-hydroxy-1,4-naphthoquinone and 5,8-dihydroxy-1,4-naphthoquinone
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference33 articles.
1. Biotransformations in the Synthesis of Enantiopure Bioactive Molecules
2. Highly Functionalized Cyclohexenyl Systems: Enzymatic Resolution and Selective Oxirane Opening Reactions of p-Benzoquinone Derivatives
3. Enzymatic resolution of diols derived from p -benzoquinones
4. Enzymic Resolution of a C2 Symmetric Diol Derived from p-Benzoquinone: Synthesis of (+)- and (-)-Bromoxone
5. Sonogashira Coupling of 2-Iodo-2-cycloalkenones: Synthesis of (+)- and (−)-Harveynone and (−)-Tricholomenyn A
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2. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase;European Journal of Medicinal Chemistry;2019-04
3. Chromophores in cellulosics, XVIII. Degradation of the cellulosic key chromophore 5,8-dihydroxy-[1,4]-naphthoquinone under conditions of chlorine dioxide pulp bleaching: a combined experimental and theoretical study;Cellulose;2018-07-04
4. Total Synthesis and Structural Determination of XR774, a Tyrosine Kinase Inhibitor;The Journal of Organic Chemistry;2018-01-16
5. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction;Bioorganic & Medicinal Chemistry Letters;2013-08
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