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 6, Pages 502–522
DOI: https://doi.org/10.1070/RC2014v083n06ABEH004419
(Mi rcr700)
 

This article is cited in 22 scientific papers (total in 22 papers)

Azodicarboxylates: synthesis and functionalization of organic compounds

A. M. Zhirov, A. V. Aksenov

North-Caucasus Federal University
English full-text Citations (22)
Abstract: Published data on the transformations of dialkyl azodicarboxylates and their analogues involving various substrates are generalized. Nucleophilic addition, oxidation, pericyclic reactions and processes occurring under Mitsunobu reaction conditions are considered. The broad scope of application of these compounds in fine organic synthesis is demonstrated.
Bibliography — 245 references.
Received: 08.07.2013
Russian version:
Uspekhi Khimii, 2014, Volume 83, Issue 6, Pages 502–522
DOI: https://doi.org/10.1070/RC2014v083n06ABEH004419
Bibliographic databases:
Language: English
Original paper language: Russian
Citation: A. M. Zhirov, A. V. Aksenov, “Azodicarboxylates: synthesis and functionalization of organic compounds”, Usp. Khim., 83:6 (2014), 502–522; Russian Chem. Reviews, 83:6 (2014), 502–522
Citation in format AMSBIB
\Bibitem{ZhiAks14}
\by A.~M.~Zhirov, A.~V.~Aksenov
\paper Azodicarboxylates: synthesis and functionalization of organic compounds
\jour Usp. Khim.
\yr 2014
\vol 83
\issue 6
\pages 502--522
\mathnet{http://mi.mathnet.ru/rcr700}
\crossref{https://doi.org/10.1070/RC2014v083n06ABEH004419}
\elib{https://elibrary.ru/item.asp?id=21818593}
\transl
\jour Russian Chem. Reviews
\yr 2014
\vol 83
\issue 6
\pages 502--522
\crossref{https://doi.org/10.1070/RC2014v083n06ABEH004419}
\isi{https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Publons&SrcAuth=Publons_CEL&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=000339992100002}
\elib{https://elibrary.ru/item.asp?id=24062972}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84903582565}
Linking options:
  • https://www.mathnet.ru/eng/rcr700
  • https://doi.org/10.1070/RC2014v083n06ABEH004419
  • https://www.mathnet.ru/eng/rcr/v83/i6/p502
  • This publication is cited in the following 22 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:165
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2024