Chemistry of Pyrazole-3(5)-Diazonium Salts (Review)* View Full Text


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Article Info

DATE

2014-11-20

AUTHORS

I. V. Ledenyova, V. V. Didenko, Kh. S. Shikhaliev

ABSTRACT

The methods of synthesis, structure, reactivity, and synthetic utility of pyrazole-3(5)-diazonium salts are reviewed here for the first time, with emphasis on heterocyclization reactions of these compounds.

PAGES

1214-1243

References to SciGraph publications

  • 1981-01. Advances in the chemistry of pyrazolidones, iminopyrazolidines, and amino- and hydroxypyrazoles (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1984-04. Studies on 5-aminopyrazole derivatives synthesis of some new fused pyrazole derivatives in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 1984-12. Characteristic features of diazotization of 5,4- and 4,5-aminonitropyrazoles and reduction of 5-arylazo-1-methyl-4-nitropyrazoles in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1980-05. Heterocyclic diazo compounds as starting materials in organic synthesis (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2007-08-13. Synthesis of Some 1,3-Thiazole, 1,3,4-Thiadiazole, Pyrazolo[5,1-c]-1,2,4-triazine, and 1,2,4-Triazolo[5,1-c]-1,2,4-triazine Derivatives Based on the Thiazolo[3,2-a]benzimidazole Moiety in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 1987-09. Reactions with heterocyclic amidines (VI): Synthesis of some new sym. and assym. pyrazolotriazines and pyrazolo[4,5-e]pyrimidine derivatives in ARCHIVES OF PHARMACAL RESEARCH
  • 1986-05. Nitroazines. 5. Use of the japp-klingemann reaction for the synthesis of nitrotriazines in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1970-02. Heterocyclic nitro compounds in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1990-09. Synthesis and antiviral activity of 6-nitro-7-oxo-4,7-dihydroazolo-[5,1-c] [1,2,4]-triazines in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 1979-06. Synthesis of o-bisazo-1H-pyrazoles and study of their cyclization to give compounds with a 1,2,4-triazine ring in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2004-11. Novel method for synthesis of polynuclear heterocyclic systems with a pyridazine ring in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2009-02. Synthesis of 7,8-dihydro-6H-pyrazolo[5',1':3,4][1,2,4]-triazino[6,5-d][1,2]diazepin-6-one, a new heterocyclic system in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1981-02. Reactions with heterocyclic amidines, VII: Synthesis of some new pyrazolo[1,5-c]-1,2,4-triazines, pyrazolo[1,5-a]-1,3,5-triazines and pyrazolo[1,5-a]pyrimidines in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 1978-03. Synthesis of o-azobispyrazole derivatives in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-014-1585-1

    DOI

    http://dx.doi.org/10.1007/s10593-014-1585-1

    DIMENSIONS

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