REACTIONS OF TRIAZINES AND TETRAZINES WITH DIENOPHILES

Authors

  • А. М. Прохоров Ural Federal University named after the First President of Russia B. N. Yeltsin
  • Д. Н. Кожевников Ural Federal University named after the First President of Russia B. N. Yeltsin; I. Ya. Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences

DOI:

https://doi.org/10.1007/1006

Keywords:

azadienes, pyridazines, pyridines, pyrimidines, tetrazines, triazines, Diels–Alder reaction

Abstract

Information on the development of a valuable synthetic methodology based on inverse electron-demand Diels–Alder reaction in the series of π-deficient azadienes (triazines and tetrazines) is summarized and classified. By this method it is possible to obtain mono-, di-, and triazines containing functional substituents both from the initial azine and from the dienophile. Such reactions are often the simplest and even the only possible method for the synthesis of substances with properties suitable for practical applications.

Authors: A. M. Prokhorov and D. N. Kozhevnikov

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (8), pp 1153-1176

http://link.springer.com/article/10.1007/s10593-012-1117-9

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Published

2013-10-14

Issue

No. 8 (2012)

Section

Review Articles