Synthesis of (3-Hydroxyadamantan-1-yl)methanols View Full Text


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Article Info

DATE

2018-09

AUTHORS

E. A. Ivleva, A. V. Pogulyaiko, Yu. N. Klimochkin

ABSTRACT

A convenient procedure has been developed for the synthesis of (3-hydroxyadamantan-1-yl)-methanols on the basis of nitroxylation of adamantan-1-ylmethanols with fuming nitring acid and subsequent reduction of intermediate nitric acid esters with hydrazine hydrate. The title diols have also been obtained by the reduction of 1-nitroxy-3-(nitroxymethyl)adamantanes. The nitroxylation process is accompanied by oxidation with the formation of substituted adamantane-1-carboxylic acids. More... »

PAGES

1294-1300

References to SciGraph publications

  • 2016-11. Synthesis of adamantane functional derivatives basing on N-[(adamantan-1-yl)alkyl]acetamides in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2016-12. Synthesis and study of basic hydrolysis of novel derivatives of N-[(adamantan-1-yl)methyl]aniline in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 1992-07. Antiviral activity of adamantane series hydroxy derivatives in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2013-01. Arylation of adamantanamines: VI. Palladium-catalyzed arylation of amines and diamines of the adamantane series with 3-bromopyridine in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2016-09. Diesters of adamantanecarboxylic acids as promising components of base stocks for industrial synthetic oils in PETROLEUM CHEMISTRY
  • 1985-09. Adamantanol nitrates in nucleophilic substitution reactions in RUSSIAN CHEMICAL BULLETIN
  • 1989-04. Synthesis and antiviral activity of nitrogen-containing adamantane derivatives in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2017-06. 1,3,5,7-Tetrasubstituted adamantanes as frameworks in the design of assemblies of porphyrin macrocycles in DOKLADY CHEMISTRY
  • 1990-01. Synthesis and biological activity of some 1-hydroxy-3-aminoalkyladamantanes and their derivatives in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2015-07. Antiviral properties of cage compounds. New prospects in RUSSIAN CHEMICAL BULLETIN
  • 2015-02. Synthesis of polycarboxylic acids of adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2017-07. One-pot synthesis of cage alcohols in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2015-03-18. Diesters of mixed carboxylic acids of the adamantane series: Synthesis, physicochemical properties, and thermo-oxidative stability in PETROLEUM CHEMISTRY
  • 2017-04-12. Synthesis and Antiviral Properties of Ethyl(3-ethyladamant-1-yl)carbamate in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 1976-11. Synthesis of dicarboxylic acids of adamantane series in RUSSIAN CHEMICAL BULLETIN
  • 2017-03. Oxidative functionalization of adamantanes (review) in PETROLEUM CHEMISTRY
  • 2015-11-04. Diesters of dicarboxylic acids of the adamantane series: Synthesis, physicochemical properties, and thermo-oxidative stability in PETROLEUM CHEMISTRY
  • 2017-09. Organic chemistry. History and mutual relations of universities of Russia in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2016-05. Biological Activity of Adamantane-Containing Mono- and Polycyclic Pyrimidine Derivatives* (A Review) in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2016-10. Synthesis of amino polycarboxylic acids of the adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2017-05. Potential synthetic adaptogens: IV. Synthesis and study of basicity of new N-[(adamantan-1-yl)methyl]aniline derivatives in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
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    http://dx.doi.org/10.1134/s107042801809004x

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