Loading [MathJax]/jax/output/SVG/config.js
Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 2014, Volume 24, Issue 5, Pages 260–261
DOI: https://doi.org/10.1016/j.mencom.2014.09.003
(Mi mendc2544)
 

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

Communications

Syntheses of spiroindole melatonin analogues via 2-(indolin-3-ylidene)acetonitrile cycloadditions

N. A. Lozinskaya, M. S. Volkova, M. Yu. Seliverstov, V. V. Temnov, S. E. Sosonyuk, M. V. Proskurnina, N. S. Zefirov

Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
Full-text PDF (237 kB) Citations (8)
Abstract: 2-(2-Oxo-1,2-dihydro-3H-indol-3-ylidene)acetonitriles were subjected to cycloaddition reactions at the double bond affording spiroindole melatonin analogues.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (398.8 Kb)


Citation: N. A. Lozinskaya, M. S. Volkova, M. Yu. Seliverstov, V. V. Temnov, S. E. Sosonyuk, M. V. Proskurnina, N. S. Zefirov, “Syntheses of spiroindole melatonin analogues via 2-(indolin-3-ylidene)acetonitrile cycloadditions”, Mendeleev Commun., 24:5 (2014), 260–261
Linking options:
  • https://www.mathnet.ru/eng/mendc2544
  • https://www.mathnet.ru/eng/mendc/v24/i5/p260
  • This publication is cited in the following 8 articles:
    1. Hao Wei, Yujie Zhang, Sanlin Jin, Ying Yu, Ning Chen, Jiaxi Xu, Zhanhui Yang, “PyBox–La(OTf)3-Catalyzed Enantioselective Diels–Alder Cycloadditions of 2-Alkenoylpyridines with Cyclopentadiene”, Molecules, 29:13 (2024), 2978  crossref
    2. Maria S. Volkova, Alexander M. Efremov, Elena N. Bezsonova, Michael D. Tsymliakov, Anita I. Maksutova, Maria A. Salykina, Sergey E. Sosonyuk, Elena F. Shevtsova, Natalia A. Lozinskaya, “Synthesis of New 2,3-Dihydroindole Derivatives and Evaluation of Their Melatonin Receptor Binding Affinity”, Molecules, 27:21 (2022), 7462  crossref
    3. Konstantin V. Balakin, Rosanna Filosa, Sergey N. Lavrenov, Arthur S. Mkrtchyan, Maxim B. Nawrozkij, Ivan A. Novakov, “Arbidol: a quarter-century later. Past, present and future of the original Russian antiviral”, Russian Chem. Reviews, 87:6 (2018), 509–552  mathnet  mathnet  crossref  isi  scopus
    4. Ekaterina V. Zaryanova, Nataly A. Lozinskaya, Olga V. Beznos, Maria S. Volkova, Nataly B. Chesnokova, Nikolay S. Zefirov, “Oxindole-based intraocular pressure reducing agents”, Bioorganic & Medicinal Chemistry Letters, 27:16 (2017), 3787  crossref
    5. N.B. Chesnokova, O.V. Beznos, N.A. Lozinskaya, M.S. Volkova, E.V. Zaryanova, N.A. Zefirov, A.V. Grigoryev, “Novel agonists of melatonin receptors as promising hypotensive and neuroprotective agents for therapy of glaucoma”, BIOMED KHIM, 63:1 (2017), 75  crossref
    6. N. B. Chesnokova, O. V. Beznos, N. A. Lozinskaya, M. S. Volkova, E. V. Zaryanova, N. S. Zefirov, A. V. Grigoryev, “Novel agonists of melatonin receptors as promising hypotensive and neuroprotective agents for therapy of glaucoma”, Biochem. Moscow Suppl. Ser. B, 11:3 (2017), 272  crossref
    7. Yan Lu, Yuhang Zhou, Lili Lin, Haifeng Zheng, Kai Fu, Xiaohua Liu, Xiaoming Feng, “N,N′-Dioxide/nickel(ii)-catalyzed asymmetric Diels–Alder reaction of cyclopentadiene with 2,3-dioxopyrrolidines and 2-alkenoyl pyridines”, Chem. Commun., 52:53 (2016), 8255  crossref
    8. Jing Peng, Guang-Yao Ran, Wei Du, Ying-Chun Chen, “Divergent Cyclization Reactions of Morita–Baylis–Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles”, Org. Lett., 17:18 (2015), 4490  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:36
    Full-text PDF :5
     
      Contact us:
    math-net2025_05@mi-ras.ru
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025