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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
Article
  • 52 Downloads

Abstract

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.

Keywords

Ester Bromide Organic Chemistry Spectral Data Phytohormonal Activity 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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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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