Loading [MathJax]/jax/output/SVG/config.js
Russian Chemical Reviews
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive
Impact factor
Guidelines for authors

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Usp. Khim.:
Year:
Volume:
Issue:
Page:
Find






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


Russian Chemical Reviews, 2015, Volume 84, Issue 11, Pages 1077–1099
DOI: https://doi.org/10.1070/RCR4562
(Mi rcr4075)
 

This article is cited in 36 scientific papers (total in 36 papers)

$C_2$-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis

S. G. Zlotin, S. V. Kochetkov

N.D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences
Abstract: The review is devoted to the application of $C_2$-symmetric diamines and their derivatives as organocatalysts for asymmetric reactions (aldol, Michael, Mannich, Diels–Alder reactions, desymmetrization, allylation, etc.). Amino acid derivatives, di- and polyamides (sulfamides), bisureas, bisthioureas, bisamidines and bisguanidines are considered. Significant attention is given to the effect of the catalyst structure on the mechanism of catalytic action. Successful applications of such catalysts in enantioselective synthesis of chiral biologically active compounds are summarized.
The bibliography includes 181 references.
Received: 23.03.2015
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: S. G. Zlotin, S. V. Kochetkov, “$C_2$-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis”, Russian Chem. Reviews, 84:11 (2015), 1077–1099
Citation in format AMSBIB
\Bibitem{ZloKoc15}
\by S.~G.~Zlotin, S.~V.~Kochetkov
\paper $C_2$-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis
\jour Russian Chem. Reviews
\yr 2015
\vol 84
\issue 11
\pages 1077--1099
\mathnet{http://mi.mathnet.ru/eng/rcr4075}
\crossref{https://doi.org/10.1070/RCR4562}
\isi{https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Publons&SrcAuth=Publons_CEL&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=000366096500001}
\elib{https://elibrary.ru/item.asp?id=25005231}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84949895359}
Linking options:
  • https://www.mathnet.ru/eng/rcr4075
  • https://doi.org/10.1070/RCR4562
  • https://www.mathnet.ru/eng/rcr/v84/i11/p1077
  • This publication is cited in the following 36 articles:
    1. Akash Mishra, Stephen Hanessian, Synthesis, 2024  crossref
    2. Elena S. Filatova, Olga V. Fedorova, Irina G. Ovchinnikova, Sergei V. Kochetkov, Konstantin A. Chistiakov, Gennady L. Rusinov, ChemistrySelect, 9:17 (2024)  crossref
    3. P. A. Mankova, A. N. Reznikov, V. A. Shiryaev, I. M. Tkachenko, Yu. N. Klimochkin, Russ J Org Chem, 59:3 (2023), 383  crossref
    4. Jun-Bo Chen, Wen-Kai Liu, Jia-Xin Song, Zheng Wang, Xing-Wang Wang, Org. Lett., 25:6 (2023), 912  crossref
    5. P. A Mankova, A. N Reznikov, V. A Shiryaev, I. M Tkachenko, Y. N Klimochkin, Žurnal organičeskoj himii, 59:3 (2023), 338  crossref
    6. Kovalevsky R.A., Kucherenko A.S., Korlyukov A.A., Zlotin S.G., Adv. Synth. Catal., 364:2 (2022), 426–439  crossref  isi
    7. Apel C., Christmann M., Tetrahedron, 82 (2021), 131760  crossref  isi
    8. Man'kova P.A., Reznikov A.N., Shiryaev V.A., Baimuratov M.R., Rybakov V.B., Klimochkin Yu.N., Russ. J. Organ. Chem., 57:2 (2021), 226–236  crossref  isi  scopus
    9. H.-X. Duan, Y. Zhang, Zh.-Zh. Zhang, Y.-Q. Wang, J. Org. Chem., 85:17 (2020), 11331–11339  crossref  isi  scopus
    10. R. Hensienne, J.-Ph. Cusson, E. Chenard, S. Hanessian, Can. J. Chem., 98:6, SI (2020), 292–306  crossref  isi  scopus
    11. V. A. Pavlov, Ya. V. Shushenachev, S. G. Zlotin, Symmetry-Basel, 11:5 (2019), 649  crossref  isi
    12. K. C. Bhowmick, M. Bihani, J. C.-G. Zhao, Mini-Rev. Org. Chem., 15:1 (2018), 3–19  crossref  isi  scopus
    13. P. Roszkowski, J. K. Maurin, Z. Czarnocki, Tetrahedron Lett., 59:22 (2018), 2184–2188  crossref  isi  scopus
    14. M. Fattahi, A. Davoodnia, N. Tavakoli-Hoseini, Heterocycl. Lett., 8:2 (2018), 449–454  isi
    15. M. Dajek, R. Kowalczyk, P. J. Boratynski, Catal. Sci. Technol., 8:17 (2018), 4358–4363  crossref  isi  scopus
    16. S. Canellas, P. Alonso, M. A. Pericas, Org. Lett., 20:16 (2018), 4806–4810  crossref  isi  scopus
    17. O. V. Fedorova, Yu. A. Titova, I. G. Ovchinnikova, G. L. Rusinov, V. N. Charushin, Mendeleev Commun., 28:4 (2018), 357–358  crossref  isi  scopus
    18. G. Szollosi, V. Kozma, ChemCatChem, 10:19 (2018), 4362–4368  crossref  isi  scopus
    19. V. A. Pavlov, S. G. Zlotin, Curr. Org. Chem., 22:21 (2018), 2029–2054  crossref  isi  scopus
    20. Y.-Y. Huang, Z.-Ch. Lv, X. Yang, Zh.-L. Wang, X.-X. Zou, Zh.-N. Zhao, F. Chen, Green Chem., 19:4 (2017), 924–927  crossref  isi  scopus
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Успехи химии Russian Chemical Reviews
    Statistics & downloads:
    Abstract page:137
     
      Contact us:
    math-net2025_03@mi-ras.ru
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025