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Dondoni, A., Massi, A., Sabbatini, S. and Bertolasi, V. (2002) Three-Component Biginelli Cyclocondensation Reaction Using C-Glycosylated Substrates. Preparation of a Collection of Dihydropyrimidinone Glycoconjugates and the Synthesis of C-Glycosylated Monastrol Analogues. Journal of Organic Chemistry, 67, 6979-6994.
https://doi.org/10.1021/jo0202076

has been cited by the following article:

• TITLE: A Novel Dihydropyridines C-Glycosylated Compound by Hantzsch Cyclo-Condensation

  AUTHORS: Soheila Sedaghat, Shabnam Madjdpour

  KEYWORDS: 1, 4-Dihydropyridines, c-Glycosylated, Multi Component Reaction, Hantzsch Reaction

  JOURNAL NAME: Open Journal of Synthesis Theory and Applications, Vol.7 No.2, April 28, 2018

  ABSTRACT: The Hantzsch synthesis has been used for the preparation of the 1,4-Dihydropyridines compounds with different pharmacophore groups. The use of a designed glycosylated compound in Hantzsch synthesis would lead to a novel Dihydropyridines C-Glycosylated compound. We used the 6-methoxy-2, 2-dimethyltetrahydrofuro [3, 4-d] [1, 3] dioxole-4-carbaldehyde as a glycosylated-based aldehydes. The 4-(3,4-Dihydroxy-5-methoxy-tetrahydro-furan-2-yl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxy-lic acid 3-ethyl ester 5-methyl ester was synthesized. The structure of compounds was determined by NMR spectroscopy, FTIR and mass spectroscopy methods. We synthesized this 1,4-Dihydropyridines compound by ionic liquid under ultrasound irradiation as a green chemistry synthesis.