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Russian Chemical Reviews, 2014, Volume 83, Issue 4, Pages 281–298
DOI: https://doi.org/10.1070/RC2014v083n04ABEH004383
(Mi rcr691)
 

This article is cited in 11 scientific papers (total in 11 papers)

Synthesis of hydroxy derivatives of limonene

O. V. Ardashov, K. P. Volcho, N. F. Salakhutdinov

N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistryof the Siberian Branch of Russian Academy of Sciences
Abstract: Synthetic routes to mono-, di- and trihydroxy derivatives of limonene are presented. Emphasis is given to the problems of regio- and stereoselectivity of transformations. Data on the isolation from natural sources and on the biological activities of the title compounds are given.
The bibliography includes 107 references.
Received: 14.03.2013
Bibliographic databases:
Language: English
Original paper language: Russian
Citation: O. V. Ardashov, K. P. Volcho, N. F. Salakhutdinov, “Synthesis of hydroxy derivatives of limonene”, Russian Chem. Reviews, 83:4 (2014), 281–298
Citation in format AMSBIB
\Bibitem{ArdVolSal14}
\by O.~V.~Ardashov, K.~P.~Volcho, N.~F.~Salakhutdinov
\paper Synthesis of hydroxy derivatives of limonene
\jour Russian Chem. Reviews
\yr 2014
\vol 83
\issue 4
\pages 281--298
\mathnet{http://mi.mathnet.ru/eng/rcr691}
\crossref{https://doi.org/10.1070/RC2014v083n04ABEH004383}
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\elib{https://elibrary.ru/item.asp?id=21345159}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84899720035}
Linking options:
  • https://www.mathnet.ru/eng/rcr691
  • https://doi.org/10.1070/RC2014v083n04ABEH004383
  • https://www.mathnet.ru/eng/rcr/v83/i4/p281
  • This publication is cited in the following 11 articles:
    1. da Silva Cesar Emiliano Hoffmann, Gosmann G., de Andrade S.F., Mini-Rev. Med. Chem., 21:14 (2021), 1813–1829  crossref  isi
    2. M. Grabarczyk, W. Maczka, A. K. Zolnierczyk, K. Winska, Molecules, 25:20 (2020), 4840  crossref  isi  scopus
    3. O. V. Ardashov, A. V. Pavlova, A. K. Mahato, Yu. Sidorova, E. A. Morozova, D. V. Korchagina, G. E. Salnikov, A. M. Genaev, O. S. Patrusheva, N. S. Li-Zhulanov, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov, ACS Chem. Neurosci., 10:10 (2019), 4337–4349  crossref  isi  scopus
    4. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, Sh. Askarova, Nat. Prod. Commun., 13:4 (2018), 387–388  isi
    5. N. F. Salakhutdinov, K. P. Volcho, O. S. Patrusheva, Russ. Chem. Rev., 87:8 (2018), 771–796  mathnet  crossref  isi  scopus
    6. Daniyar Sadyrbekov, Timur Saliev, Yuri Gatilov, Ivan Kulakov, Roza Seidakhmetova, Tulegen Seilkhanov, Sholpan Askarova, Natural Product Communications, 13:4 (2018), 1934578X1801300  crossref
    7. N. F. Salakhutdinov, K. P. Volcho, O. I. Yarovaya, Pure Appl. Chem., 89:8 (2017), 1105–1117  crossref  isi  scopus
    8. Yu. S. Demidova, E. V. Suslov, I. L. Simakova, K. P. Volcho, E. Smolentseva, N. F. Salakhutdinov, A. Simakov, D. Yu. Murzin, Mol. Catal., 433 (2017), 414–419  crossref  isi  scopus
    9. O. V. Ardashov, K. P. Volcho, N. F. Salakhutdinov, ChemInform, 46:5 (2015), no  crossref
    10. O. V. Ardashov, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov, Chem Nat Compd, 2015  crossref  isi  scopus
    11. Ardashov O.V., Demidova Yu.S., Korchagina D.V., Volcho K.P., Simakova I.L., Salakhutdinov N.F., Helv. Chim. Acta, 98:10 (2015), 1442–1455  crossref  isi  elib  scopus
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