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Mendeleev Communications, 2017, Volume 27, Issue 5, Pages 490–492
DOI: https://doi.org/10.1016/j.mencom.2017.09.020
(Mi mendc2037)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Synthesis of natural phaeosphaeride A and semi-natural phaeosphaeride B derivatives

V. V. Abzianidzea, K. P. Efimovab, E. V. Poluektovac, Yu. G. Trishinb, V. A. Kuznetsova

a Research Institute of Hygiene, Occupational Pathology and Human Ecology, Leningrad region, Russian Federation
b Saint-Petersburg State University of Industrial Technologies and Design, St. Petersburg, Russian Federation
c All-Russian Institute of Plant Protection, Federal Agency of Scientific Organizations, Pushkin, St. Petersburg, Russian Federation
Full-text PDF (284 kB) Citations (8)
Abstract: 6-O-Acylated phaeosphaeride A and phaeosphaeride B in reaction with secondary cyclic amines undergo stereospecific replacement of acyloxy group by pharmacophoric amino moiety. In case of chloroacetoxy derivative, chlorine displacement by such amines proceeds in the presence of triethylamine.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.0 Mb)


Citation: V. V. Abzianidze, K. P. Efimova, E. V. Poluektova, Yu. G. Trishin, V. A. Kuznetsov, “Synthesis of natural phaeosphaeride A and semi-natural phaeosphaeride B derivatives”, Mendeleev Commun., 27:5 (2017), 490–492
Linking options:
  • https://www.mathnet.ru/eng/mendc2037
  • https://www.mathnet.ru/eng/mendc/v27/i5/p490
  • This publication is cited in the following 8 articles:
    1. Partha Sarathi Bera, Yafia Kousin Mirza, Tarunika Sachdeva, Milan Bera, “Recent Advances in Transition Metal-Catalyzed Ring-Opening Reaction of Aziridine”, Compounds, 4:4 (2024), 626  crossref
    2. V. V. Abzianidze, V. V. Kadochnikov, D. S. Suponina, N. V. Skvortsov, P. P. Beltyukov, V. N. Babakov, D. V. Krivorotov, E. M. Barysheva, A. V. Garabadzhiu, “X-ray structure and in silico molecular docking of a natural phaeosphaeride A derivative for targets associated with kinase cascades”, Mendeleev Commun., 33:4 (2023), 534–536  mathnet  crossref
    3. Kenichi Kobayashi, Hiroshi Kogen, Osamu Tamura, “Total Synthesis of Phaeosphaerides with STAT3 Inhibitory Activity”, J. Synth. Org. Chem. Jpn., 80:8 (2022), 755  crossref
    4. S. A. Zakharenkova, V. V. Abzianidze, N. I. Moiseeva, D. S. Lukina, L. S. Chistyi, D. V. Krivorotov, Yu. G. Trishin, “Antitumor activity of phaeosphaeride A modified with nitrogen heterocyclic groups”, Mendeleev Commun., 31:5 (2021), 662–663  mathnet  crossref
    5. Victoria V. Abzianidze, Sofya A. Zakharenkova, Natalia I. Moiseeva, Petr P. Beltyukov, Valeriy A. Polukeev, Yaroslav A. Dubrovskii, Victor A. Kuznetsov, Yuri G. Trishin, Jennifer E. Mejia, Alvin A. Holder, “Towards lead compounds as anti-cancer agents via new phaeosphaeride A derivatives”, Bioorganic & Medicinal Chemistry Letters, 29:1 (2019), 59  crossref
    6. Victoria Abzianidze, Petr Beltyukov, Sofya Zakharenkova, Natalia Moiseeva, Jennifer Mejia, Alvin Holder, Yuri Trishin, Alexander Berestetskiy, Victor Kuznetsov, “Synthesis and Biological Evaluation of Phaeosphaeride A Derivatives as Antitumor Agents”, Molecules, 23:11 (2018), 3043  crossref
    7. Kenichi Kobayashi, Kosaku Tanaka, Hiroshi Kogen, “Total Synthesis and Biological Evaluation of Phaeosphaerides”, Catalysts, 8:5 (2018), 206  crossref
    8. Ekaterina Poluektova, Yuriy Tokarev, Sofia Sokornova, Leonid Chisty, Antonio Evidente, Alexander Berestetskiy, “Curvulin and Phaeosphaeride A from Paraphoma sp. VIZR 1.46 Isolated from Cirsium arvense as Potential Herbicides”, Molecules, 23:11 (2018), 2795  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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