Chemistry of Heterocyclic Compounds

, Volume 17, Issue 10, pp 1030–1032 | Cite as

Synthesis of 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl esters of acids with phytohormonal activity. New modification of the koenigs-knorr method

  • P. S. Khokhlov
  • G. D. Sokolova
  • A. Yu. Makoveichuk
  • B. Ya. Chvertkin


2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl esters were synthesized by the reaction of tetralkylammonium salts of 4-amino-3,5,7-trichloropicolinic, 2,4-dichlorophenoxyacetic, and β-indolylacetic acids with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide. According to the PMR spectral data, substitution occurs stereospecifically to give the β anomers.


Ester Bromide Organic Chemistry Spectral Data Phytohormonal Activity 
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Copyright information

© Plenum Publishing Corporation 1982

Authors and Affiliations

  • P. S. Khokhlov
    • 1
  • G. D. Sokolova
    • 1
  • A. Yu. Makoveichuk
    • 1
  • B. Ya. Chvertkin
    • 1
  1. 1.All-Union Scientific-Research Institute of PhytopathologyMoscow Province

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