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Mendeleev Communications, 2011, Volume 21, Issue 5, Pages 247–249
DOI: https://doi.org/10.1016/j.mencom.2011.09.005
(Mi mendc2932)
 

This article is cited in 6 scientific papers (total in 6 papers)

Molecular and crystal structures of hetero-analogues of bicyclo[3.3.1]nonane with nitrogen and sulfur atoms

O. N. Zefirovaab, N. N. Moiseevaa, E. V. Nurievaa, T. P. Trofimovaa, A. N. Proshinb, Yu. L. Slovokhotovac

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (739 kB) Citations (6)
Abstract: The X-ray molecular structures of bridgehead heterocycles, namely, 3-thia-1-azabicyclo[3.3.1]nonane-2-thione, 1,3-diazabicyclo[3.3.1]nonane-2-thione, (2Z)-2-(N-benzoylimino)-3-thia-1-azabicyclo[3.3.1]nonane and (2Z)-2-(3,4-dichlorophenylimino)-3-thia-1-azabicyclo[3.3.1]nonane were determined and their molecular packing in the crystals was revealed. The rings distortion in the bridgehead core was evaluated by the calculation of ZP and CP puckering parameters.
Document Type: Article
Language: English


Citation: O. N. Zefirova, N. N. Moiseeva, E. V. Nurieva, T. P. Trofimova, A. N. Proshin, Yu. L. Slovokhotov, “Molecular and crystal structures of hetero-analogues of bicyclo[3.3.1]nonane with nitrogen and sulfur atoms”, Mendeleev Commun., 21:5 (2011), 247–249
Linking options:
  • https://www.mathnet.ru/eng/mendc2932
  • https://www.mathnet.ru/eng/mendc/v21/i5/p247
  • This publication is cited in the following 6 articles:
    1. Barbara Parrino, Stella Cascioferro, Daniela Carbone, Girolamo Cirrincione, Patrizia Diana, Comprehensive Heterocyclic Chemistry IV, 2022, 150  crossref
    2. E. V. Nurieva, T. P. Trofimova, A. A. Alexeev, A. N. Proshin, E. A. Chesnakova, Yu. K. Grishin, K. A. Lyssenko, M. V. Filimonova, S. O. Bachurin, O. N. Zefirova, “Synthesis and antihypotensive properties of 2-amino-2-thiazoline analogues with enhanced lipophilicity”, Mendeleev Commun., 28:4 (2018), 390–392  mathnet  crossref
    3. Svetlana Blokhina, Angelica Sharapova, Marina Ol'khovich, Tatyana Volkova, German Perlovich, Alexey N. Proshin, “Sublimation enthalpy of 1,3-thiazine structural analogues: Experimental determination and estimation based on structural clusterization”, Thermochimica Acta, 656 (2017), 10  crossref
    4. Svetlana V. Blokhina, Marina V. Ol'khovich, Angelica V. Sharapova, German L. Perlovich, Alexey N. Proshin, “Vapor pressures and sublimation enthalpies of novel bicyclic heterocycle derivatives”, The Journal of Chemical Thermodynamics, 69 (2014), 107  crossref
    5. E. D. Plotnikova, E. V. Nurieva, D. I. Peregud, M. V. Onufriev, N. V. Gulyaeva, V. M. Makarchuk, M. V. Filimonova, N. S. Zefirov, O. N. Zefirova, “Molecular modeling, X-ray diffraction analysis, and the study of iNOS inhibitor activity of 3-imino-2,4-diazabicyclo[3.3.1]nonan-1-ol hydrochloride”, Russ J Org Chem, 49:8 (2013), 1108  crossref
    6. A. N. Proshin, I. V. Serkov, S. O. Bachurin, “Synthesis of selenium analogs of 1-azabicyclo[3.3.1]nonane”, Dokl Chem, 443:1 (2012), 80  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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