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Mendeleev Communications, 2017, Volume 27, Issue 5, Pages 443–445
DOI: https://doi.org/10.1016/j.mencom.2017.09.003
(Mi mendc2020)
 

This article is cited in 9 scientific papers (total in 9 papers)

Communications

Novel α,β-unsaturated imine derivatives of 3-aminopropylsilatrane

S. N. Adamovicha, N. V. Vchisloa, E. N. Oborinaa, I. A. Ushakovb, I. B. Rozentsveiga

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Irkutsk National Research Technical University, Irkutsk, Russian Federation
Full-text PDF (334 kB) Citations (9)
Abstract: Novel highly functionalized and pharmacologically promising active silatranes equipped with an α,β-unsaturated imine group, Het(Ar)CH=C(SR)C(H)=N–, in the axial chain have been synthesized by the reaction of 3-aminopropylsilatrane and (Z)-2-alkylthio-3-(het)arylpropenals. The structures of these compounds were characterized by IR and 1H, 13C, 15N, 29Si, 1D and 2D NMR spectroscopy.
Document Type: Article
Language: English


Citation: S. N. Adamovich, N. V. Vchislo, E. N. Oborina, I. A. Ushakov, I. B. Rozentsveig, “Novel α,β-unsaturated imine derivatives of 3-aminopropylsilatrane”, Mendeleev Commun., 27:5 (2017), 443–445
Linking options:
  • https://www.mathnet.ru/eng/mendc2020
  • https://www.mathnet.ru/eng/mendc/v27/i5/p443
  • This publication is cited in the following 9 articles:
    1. Samir Hmaimou, Marouane Ait Lahcen, Mohamed Adardour, Mohammed M. Alanazi, Atul Kabra, Mohamed Maatallah, Abdesselam Baouid, “A Stereoselective Synthesis of a Novel α,β-Unsaturated Imine-Benzodiazepine through Condensation Reaction, Crystal Structure, and DFT Calculations”, Molecules, 29:18 (2024), 4323  crossref
    2. Nadezhda V. Vchislo, Sergey N. Adamovich, Victoria G. Fedoseeva, Elizaveta N. Oborina, Igor B. Rozentsveig, Francis Verpoort, “Schiff Base of 3‐Aminopropylalkoxysilanes and 3‐Aminopropylsilatranes: Importance of Investigations and the Potential Applications”, Applied Organom Chemis, 38:12 (2024)  crossref
    3. Mirela-Fernanda Zaltariov, Mihaela Turtoi, Dragos Peptanariu, Ana-Maria Macsim, Lilia Clima, Corneliu Cojocaru, Nicoleta Vornicu, Bianca-Iulia Ciubotaru, Alexandra Bargan, Manuela Calin, Maria Cazacu, “Chemical Attachment of 5-Nitrosalicylaldimine Motif to Silatrane Resulting in an Organic–Inorganic Structure with High Medicinal Significance”, Pharmaceutics, 14:12 (2022), 2838  crossref
    4. S. N. Adamovich, I. A. Ushakov, A. V. Afonin, N. V. Vchislo, E. N. Oborina, D. V. Pavlov, “O- and S-containing 1-azadiene derivatives of 3-aminopropylsilatrane”, Russ Chem Bull, 70:2 (2021), 406  crossref
    5. N.F. Lazareva, I.V. Sterkhova, “1-[N-phenyl(aminomethyl)]silatrane: Synthesis, reactivity and structure”, Journal of Organometallic Chemistry, 898 (2019), 120870  crossref
    6. S. N. Adamovich, E. N. Oborina, “Metallatranes and hydrometallatranes: their immunotropic and antitumor properties”, Russ Chem Bull, 68:9 (2019), 1723  crossref
    7. Z. G. Denieva, U. A. Budanova, Yu. L. Sebyakin, “Synthetic asymmetric lipid-like organosilanes for liposomal nanohybrid cerasomes toward potential medical applications”, Mendeleev Commun., 29:1 (2019), 32–34  mathnet  crossref
    8. S. N. Adamovich, V. V. Novokshonov, I. A. Ushakov, V. G. Elshina, E. N. Oborina, “New silatranes of α,β-acetylene azomethine series”, Russ Chem Bull, 67:9 (2018), 1744  crossref
    9. V. I. Smirnov, E. A. Zelbst, G. A. Kuznetsova, I. V. Sterkhova, “Crystal and molecular structures of Si-(iodomethyl)silatranes with methyl substituents in β-position relative to the nitrogen atom”, Mendeleev Commun., 28:3 (2018), 278–280  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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