EventsThe 15th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 15th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Oct, 2011
Citation
Hoai The Le, Thanh Dinh Nguyen, SOME CONVERSIONS OF PER-O-ACETYL-β-D-GLYCOPYRANOSYL THIOSEMICARBAZONES OF SUBSTITUTED ACETOPHENONES AND BENZALDEHYDES, in Proceedings of The 15th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2011, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-15-00778
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SOME CONVERSIONS OF PER-O-ACETYL-β-D-GLYCOPYRANOSYL THIOSEMICARBAZONES OF SUBSTITUTED ACETOPHENONES AND BENZALDEHYDES

Hoai The Le 1
1. College of Science, Vietnam National University (Hanoi)
Abstract
Some novel substituted acetophenone and benzaldehyde (2\',3\',4\',6\'-tetra-O-acetyl-β-D-glucopyranosyl)-thiosemicarbazones were synthesized by reaction of 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl thiosemicarbazide and substituted acetophenones and benzaldehydes. The reaction was performed using microwave-assisted method. The compounds have converted into 2-iminothiazolidin-4-ones by reaction with ethyl bromoacetate in dichloromethane in the presence of anhydrous sodium acetate. Structures of obtained compounds were confirmed by spectroscopic methods.
Keywords
acetophenone
benzaldehyde
imines
ethyl bromoacetate
INVESTIGATION OF SYNTHETIC REACTION OF AZOMETHINES FROM GLUCOSAMINE AND SUBSTITUTED BENZALDEHYDES
"Monoalkylbenzenes substituted by functional groups in the side chain. The effect of alkyl groups spatial structure on the chemical shift of aromatic ortho-protons in NMR1H spectra"