Stereoselective cycloaddition reactions of carbohydrate derivatives

Pál Herczegh, Imre Kovács, Gyöngyi Erdosi, Tamás Varga, Attila Agócs, László Szilágyi, Ferenc Sztaricskai, Amaya Berecibar, Gabor Lukacs, Alain Olesker

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Abstract

Structural analogs of swainsonine and castanospermine have been synthesized using [4+2] cycloadditions of chiral azomethines with Danishefsky diene. Similar hydroxyindolizidines were prepared by [3+2] dipolar cycloadditions of sugar derived cyclic nitrones with methyl acrylate. Stereoselectivity of [2+2] photocycloadditions of uridine derivatives was also studied.

Original languageEnglish
Pages (from-to)519-524
Number of pages6
JournalPure and Applied Chemistry
Volume69
Issue number3
DOIs
Publication statusPublished - Mar 1997

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ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

Herczegh, P., Kovács, I., Erdosi, G., Varga, T., Agócs, A., Szilágyi, L., Sztaricskai, F., Berecibar, A., Lukacs, G., & Olesker, A. (1997). Stereoselective cycloaddition reactions of carbohydrate derivatives. Pure and Applied Chemistry, 69(3), 519-524. https://doi.org/10.1351/pac199769030519