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, 2014, Volume 83, Issue 10, Pages 885–985
DOI: https://doi.org/10.1070/RC2014v83n10ABEH004471
(Mi rcr716)
 

This article is cited in 208 scientific papers (total in 208 papers)

Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision

V. P. Ananikovab, L. L. Khemchyana, Yu. V. Ivanovaa, V. I. Bukhtiyarovcd, A. M. Sorokinc, I. P. Prosvirinc, S. Z. Vatsadzee, A. V. Medved'koe, V. N. Nurieve, A. D. Dilmana, V. V. Levina, I. V. Koptyugfd, K. V. Kovtunovfd, V. V. Zhivonitkofd, V. A. Likholobovg, A. V. Romanenkoc, P. A. Simonovcd, V. G. Nenajdenkoeh, O. I. Shmatovae, V. M. Muzalevskiye, M. S. Nechaevei, A. F. Asachenkoi, O. S. Morozovi, P. B. Dzhevakovi, S. N. Osipovh, D. V. Vorobyevah, M. A. Topchiyh, M. A. Zotovah, S. A. Ponomarenkoej, O. V. Borshchevj, Yu. N. Luponosovj, A. A. Rempelkl, A. A. Valeevakl, A. Yu. Stakheeva, O. V. Turovaa, I. S. Mashkovskya, S. V. Sysolyatinm, V. V. Malykhinm, G. A. Bukhtiyarovac, A. O. Terent'eva, I. B. Krylova

a N.D. Zelinskii Institute of Organic Chemistry
b Saint Petersburg State University
c Boreskov Institute of Catalysis SB RAS, Novosibirsk
d Novosibirsk State University
e M. V. Lomonosov Moscow State University, Department of Chemistry
f International Tomography Center of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk
g Institute of Hydrocarbons Processing of SB RAS
h A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, Moscow
i A. V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow
j N. S. Enikolopov Institute of Synthetic Polymer Materials RAS, Moscow
k Institute of Solid State Chemistry, Urals Branch of the Russian Academy of Sciences, Ekaterinburg
l Ural Federal University named after the First President of Russia B. N. Yeltsin, Ekaterinburg
m Institute for Problems of Chemical and Energetic Technology, Siberian Branch of the Russian Academy of Sciences, Biisk, Altai krai
English full-text Citations (208)
Abstract: The challenges of the modern society and the growing demand of high-technology sectors of industrial production bring about a new phase in the development of organic synthesis. A cutting edge of modern synthetic methods is introduction of functional groups and more complex structural units into organic molecules with unprecedented control over the course of chemical transformation. Analysis of the state-of-the-art achievements in selective organic synthesis indicates the appearance of a new trend — the synthesis of organic molecules, biologically active compounds, pharmaceutical substances and smart materials with absolute selectivity. Most advanced approaches to organic synthesis anticipated in the near future can be defined as “atomic precision” in chemical reactions. The present review considers selective methods of organic synthesis suitable for transformation of complex functionalized molecules under mild conditions. Selected key trends in the modern organic synthesis are considered including the preparation of organofluorine compounds, catalytic cross-coupling and oxidative cross-coupling reactions, atom-economic addition reactions, methathesis processes, oxidation and reduction reactions, synthesis of heterocyclic compounds, design of new homogeneous and heterogeneous catalytic systems, application of photocatalysis, scaling up synthetic procedures to industrial level and development of new approaches to investigation of mechanisms of catalytic reactions.
The bibliography includes 840 references.
Received: 30.05.2014
Russian version:
Uspekhi Khimii, 2014, Volume 83, Issue 10, Pages 885–985
DOI: https://doi.org/10.1070/RC2014v83n10ABEH004471
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: V. P. Ananikov, L. L. Khemchyan, Yu. V. Ivanova, V. I. Bukhtiyarov, A. M. Sorokin, I. P. Prosvirin, S. Z. Vatsadze, A. V. Medved'ko, V. N. Nuriev, A. D. Dilman, V. V. Levin, I. V. Koptyug, K. V. Kovtunov, V. V. Zhivonitko, V. A. Likholobov, A. V. Romanenko, P. A. Simonov, V. G. Nenajdenko, O. I. Shmatova, V. M. Muzalevskiy, M. S. Nechaev, A. F. Asachenko, O. S. Morozov, P. B. Dzhevakov, S. N. Osipov, D. V. Vorobyeva, M. A. Topchiy, M. A. Zotova, S. A. Ponomarenko, O. V. Borshchev, Yu. N. Luponosov, A. A. Rempel, A. A. Valeeva, A. Yu. Stakheev, O. V. Turova, I. S. Mashkovsky, S. V. Sysolyatin, V. V. Malykhin, G. A. Bukhtiyarova, A. O. Terent'ev, I. B. Krylov, “Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision”, Usp. Khim., 83:10 (2014), 885–985; Russian Chem. Reviews, 83:10 (2014), 885–985
Citation in format AMSBIB
\Bibitem{AnaKheIva14}
\by V.~P.~Ananikov, L.~L.~Khemchyan, Yu.~V.~Ivanova, V.~I.~Bukhtiyarov, A.~M.~Sorokin, I.~P.~Prosvirin, S.~Z.~Vatsadze, A.~V.~Medved'ko, V.~N.~Nuriev, A.~D.~Dilman, V.~V.~Levin, I.~V.~Koptyug, K.~V.~Kovtunov, V.~V.~Zhivonitko, V.~A.~Likholobov, A.~V.~Romanenko, P.~A.~Simonov, V.~G.~Nenajdenko, O.~I.~Shmatova, V.~M.~Muzalevskiy, M.~S.~Nechaev, A.~F.~Asachenko, O.~S.~Morozov, P.~B.~Dzhevakov, S.~N.~Osipov, D.~V.~Vorobyeva, M.~A.~Topchiy, M.~A.~Zotova, S.~A.~Ponomarenko, O.~V.~Borshchev, Yu.~N.~Luponosov, A.~A.~Rempel, A.~A.~Valeeva, A.~Yu.~Stakheev, O.~V.~Turova, I.~S.~Mashkovsky, S.~V.~Sysolyatin, V.~V.~Malykhin, G.~A.~Bukhtiyarova, A.~O.~Terent'ev, I.~B.~Krylov
\paper Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision
\jour Usp. Khim.
\yr 2014
\vol 83
\issue 10
\pages 885--985
\mathnet{http://mi.mathnet.ru/rcr716}
\crossref{https://doi.org/10.1070/RC2014v83n10ABEH004471}
\elib{https://elibrary.ru/item.asp?id=21948604}
\transl
\jour Russian Chem. Reviews
\yr 2014
\vol 83
\issue 10
\pages 885--985
\crossref{https://doi.org/10.1070/RC2014v83n10ABEH004471}
\isi{https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Publons&SrcAuth=Publons_CEL&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=000344941600002}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84907452759}
Linking options:
  • https://www.mathnet.ru/eng/rcr716
  • https://doi.org/10.1070/RC2014v83n10ABEH004471
  • https://www.mathnet.ru/eng/rcr/v83/i10/p885
  • This publication is cited in the following 208 articles:
    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:831
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2024