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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 27, 1997 - Issue 1
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Original Articles

A Convenient Method for the Selective Alkylation ofβ-OH Groups of 2(3)-Hydroxyjuglones and Hydroxynaphthazarines

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Pages 119-126 | Received 05 Jul 1996, Published online: 19 Aug 2006

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VictorPh. Anufriev, GalinaV. Malinovskaya, VyacheslavL. Novikov, NadezhdaN. Balanyova & SergeyG. Polonik. (1998) The Reductive Dehalogenation of Halo-Substituted Naphthazarins and Quinizarins as a Simple Route to Parent Compounds. Synthetic Communications 28:12, pages 2149-2157.
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Articles from other publishers (12)

N. N. Balaneva, O. P. Shestak & V. L. Novikov. (2019) Trimethyl orthoacetate as a convenient reagent for selective methylation of β-OH groups of (poly)hydroxynaphthazarins. Russian Chemical Bulletin 68:1, pages 55-63.
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Nadezhda N. Balaneva, Olga P. Shestak & Vyacheslav L. Novikov. (2018) The Use of Trimethyl Orthoacetate for the Conversion of Natural Mono- and Dihydroxynaphthazarins and Related Compounds to Their Methyl Ethers. Natural Product Communications 13:10, pages 1934578X1801301.
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N. N. Balaneva, O. P. Shestak, V. F. Anufriev & V. L. Novikov. (2016) Synthesis of Spinochrome D, A Metabolite of Various Sea-Urchin Species. Chemistry of Natural Compounds 52:2, pages 213-217.
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Olga P. Shestak, Victor Ph. Anufriev & Vyacheslav L. Novikov. (2014) Preparative Production of Spinochrome E, a Pigment of Different Sea Urchin Species. Natural Product Communications 9:7, pages 1934578X1400900.
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K. L. Borisova & V. F. Anufriev. (2012) Simple preparative synthesis of spinochrome e, a pigment from sea urchins of the genus Echinothrix. Chemistry of Natural Compounds 48:2, pages 202-204.
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K. L. Borisova, G. I. Mel’man, V. A. Denisenko, V. P. Glazunov & V. F. Anufriev. (2012) Conversion of 2,3-dihydroxynaphthazarins to isoquinoline-1,3,4(2H)-trione derivatives. Russian Chemical Bulletin 61:3, pages 616-622.
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N. D. Pokhilo, M. I. Kiseleva & V. F. Anufriev. (2011) Synthesis and cytotoxic activity of azidonaphthazarins. Pharmaceutical Chemistry Journal 45:9, pages 522-525.
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A. Ya. Yakubovskaya, N. D. Pokhilo, V. F. Anufriev & M. M. Anisimov. (2009) Synthesis and antimicrobial and antifungal activities of compounds of the naphthazarin series. Pharmaceutical Chemistry Journal 43:7.
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N. D. Pokhilo, A. Ya. Yakubovskaya, V. F. Anufriev & D. V. Berdyshev. (2007) Chemistry of naphthazarine derivatives: XIV. Preparative synthesis of 1′-bromoalkylnaphthazarines. Russian Journal of Organic Chemistry 43:8, pages 1170-1175.
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G. V. Malinovskaya, V. F. Anufriev & V. P. Glazunov. (2000) Catalytic activity of sorbents containing metals, and nucleophilicity of alcohols activated with fluoride anion in reaction of nucleophilic substitution in 2,3-dichloronaphthazarines. Russian Journal of Electrochemistry 36:6, pages 843-846.
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Victor Ph. Anufriey, Vyacheslav L. Novikov, Oleg B. Maximov, George B. Elyakov, Dmitry O. Levitsky, Alexander V. Lebedev, Safa M. Sadretdinov, Alexei V. Shvilkin, Natalya I. Afonskaya, Mikhail Ya. Ruda & Nina M. Cherpachenko. (1998) Synthesis of some hydroxynaphthazarins and their cardioprotective effects under ischemia-reperfusion in vivo. Bioorganic & Medicinal Chemistry Letters 8:6, pages 587-592.
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V. PH. ANUFRIEV, V. L. NOVIKOV, G. V. MALINOVSKAYA & V. P. GLAZUNOV. (2010) ChemInform Abstract: A Convenient Method for the Selective Alkylation of β-OH Groups of 2(3)-Hydroxyjuglones and Hydroxynaphthazarines.. ChemInform 28:22, pages no-no.
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