E. E. APENOVA

N.D. Zelinsky Institute of Organic Chemistry

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Yu. A. Sharanin

Luhansk State Medical University

ВП

В. П. Литвинов

N.D. Zelinsky Institute of Organic Chemistry

ВП

В. П. Литвинов

N.D. Zelinsky Institute of Organic Chemistry

V. Yu. Mortikov

N.D. Zelinsky Institute of Organic Chemistry

АМ

А. М. Шестопалов

Federal Research Center of Fundamental and Translational Medicine

Yu. T. Struchkov

A. N. Nesmeyanov Institute of Organoelement Compounds

T. B. Asadullaev

Russian Academy of Sciences

Vladimir N. Nesterov

University of North Texas

V. E. Shklover

University of Luhansk

Ikram Abdullaev

Urgench State University

Cooperative Institutions

Russian Academy of Sciences

N.D. Zelinsky Institute of Organic Chemistry

A. N. Nesmeyanov Institute of Organoelement Compounds

University of Luhansk

Luhansk State Medical University

Pskov State Pedagogical Institute

Azerbaijan National Academy of Sciences

University of North Texas

New Mexico Highlands University

Volgograd State University of Architecture and Civil Engineering

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ChemInform Abstract: SYNTHESIS OF 6‐(1‐ADAMANTYL)‐3‐CYANOPYRIDIN‐2(1H)‐ONE AND ‐SELENONE

Chemischer Informationsdienst (1985)

В. П. Литвинов E. E. APENOVA Yu. A. Sharanin А. М. Шестопалов

Abstract Durch Umsetzen der 1‐Adamantylverbindung (I) mit Cyanacetamid bzw. mit Cyanselenoacetamid werden die bisher nicht beschriebenen Titelverbindungen (II) bzw. (III) erhalten.

10.1002/chin.198533300

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ChemInform Abstract: Hetaryladamantanes. Part 5. Synthesis of 6‐(Adamantyl‐1)‐3‐cyanopyridine‐ 2(1H)‐selenone and Substituted Selenophenopyridines on Its Basis.

Chemischer Informationsdienst (1986)

E. E. APENOVA Yu. A. Sharanin B. M. Zolotarev V. P. LITBINOV

Abstract Durch Umsetzung des Natriumsalzes von 3‐Adamantyl‐1‐hydroxypropenon‐3 (I) mit Cyanselenoacetamid (II) wird das Adamantyl‐selenopyridon (III) erhalten, das mit den Halogenverbindungen (IV) über die Selenoether (V) die Adamantyl‐substituierten Selenophenopyridine‐ (VI) ergibt.

Basis (linear algebra)

10.1002/chin.198636260

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ChemInform Abstract: Fused Pyridines. Part 6. The Synthesis and Structure of Adamantyl‐, Cyclopropyl‐, and Alkyl‐Substituted 3‐Halomethyl‐2,3‐dihydro‐8‐cyanothiazolo‐(oxazolo, selenazolo)(3,2‐a)pyridinium Salts.

ChemInform (1987)

В. П. Литвинов Yu. A. Sharanin E. E. APENOVA A. M. Shestopalov V. Yu. Mortikov

10.1002/chin.198751224

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Synthesis of 6-(adamantyl-1)-3-cyano-2(1H)-pyridinethione

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science (1984)

В. П. Литвинов E. E. APENOVA Yu. A. Sharanin А. М. Шестопалов

10.1007/bf00954127

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Citations (1)

Heteryladamantanes. Communication 6. Synthesis and some properties of 6-(1-adamantyl)-3-cyanopyridin-2(1H)-one

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science (1987)

В. П. Литвинов E. E. APENOVA Yu. A. Sharanin

10.1007/bf00959379

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Citations (1)

ChemInform Abstract: SYNTHESIS OF 6‐(ADAMANT‐1‐YL)‐3‐CYANO‐2(1H)‐PYRIDINETHIONE

Chemischer Informationsdienst (1985)

В. П. Литвинов E. E. APENOVA Yu. A. Sharanin А. М. Шестопалов

10.1002/chin.198514260

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Crystal structure of 6-(1-adamantyl)-3-cyanopyridine-2(1H)-selenone

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science (1988)

Vladimir N. Nesterov V. E. Shklover Yu. T. Struchkov В. П. Литвинов E. E. APENOVA

Crystal (programming language)

10.1007/bf00957459

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Citations (3)

ChemInform Abstract: Synthesis and Antiviral Activity of 3‐Cyano‐2(1H)‐pyridineselones.

ChemInform (1992)

V. Yu. Mortikov В. П. Литвинов А. М. Шестопалов Yu. A. Sharanin E. E. APENOVA

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

10.1002/chin.199239247

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Synthesis and antiviral activity of 3-cyano-2(1H)pyridine selenones

Pharmaceutical Chemistry Journal (1991)

V. Yu. Mortikov В. П. Литвинов А. М. Шестопалов Yu. A. Sharanin E. E. APENOVA

10.1007/bf00772121

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Citations (6)

ChemInform Abstract: Heteroaryladamantane. Part 4. Synthesis, Structure and Properties of 6-(Adamantyl- 1)-3-cyanopyridine-2-(1H)-thione.

Chemischer Informationsdienst (1986)

В. П. Литвинов E. E. APENOVA Yu. A. Sharanin Vladimir N. Nesterov V. E. Shklover

Abstract Aus dem Adamantylmethylketon (I) erhält man über das Ketoenolat (III) das Pyridinthion (V), das leicht zu dem Disulfid (VI) oxidiert wird.′ Die Umsetzung von (V) mit den Alkylierungsmitteln (VII) führt zu 86 den Thioethern (VIII) bzw. zu den Thienopyridinen (IX).

10.1002/chin.198628237

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