Russian Chemical Bulletin

, Volume 51, Issue 5, pp 854–859

Application of the Thorpe—Ziegler reaction for the synthesis of functionalized thiophenes, thienopyrimidines, and thienotriazines

Authors

  • S. A. Ryndina
    • State Scientific Center of the Russian Federation “Organic Intermediate Products and Dyes Institute” (NIOPIK)
  • A. V. Kadushkin
    • State Scientific Center of the Russian Federation “Organic Intermediate Products and Dyes Institute” (NIOPIK)
  • N. P. Solov"eva
    • Center of Drug ChemistryAll-Russian Research Chemical Pharmaceutical Institute
  • V. G. Granik
    • State Scientific Center of the Russian Federation “Organic Intermediate Products and Dyes Institute” (NIOPIK)
Article

DOI: 10.1023/A:1016049204323

Cite this article as:
Ryndina, S.A., Kadushkin, A.V., Solov"eva, N.P. et al. Russian Chemical Bulletin (2002) 51: 854. doi:10.1023/A:1016049204323

Abstract

Approaches to the synthesis of 3-aminothiophene-2,4-dicarboxylic acid derivatives and to their conversions into thieno[3,4-d]pyrimidines, thieno[3,4-d]-1,2,3-triazines, and thieno[3,2-d]pyrimidines are developed.

enaminesthe Thorpe—Ziegler cyclizationthiophenespyrimidines1,2,3-triazines
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Copyright information

© Plenum Publishing Corporation 2002