Molecules (Aug 2008)

Synthesis of a Novel D-Glucose-Conjugated 15-Crown-5 Ether with a Spiro Ketal Structure

  • Sho Matsuda,
  • Hitomi Muraishi,
  • Yoshiki Oda,
  • Takashi Yamanoi

DOI
https://doi.org/10.3390/molecules13081840
Journal volume & issue
Vol. 13, no. 8
pp. 1840 – 1845

Abstract

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Abstract: This paper describes a synthetic approach to a novel D-glucose-conjugated 15-crown-5 ether having a spiroketal structure starting from a 1-C-vinylated glucose derivative. The approach consists of the glycosylation of the vinylated glucose derivative to give an ethyleneoxy spacer derivative using bismuth(III) triflate, the conversion of the 1-C-vinyl group of the glucoside produced into a carboxylic acid group, and the intramolecular condensation between the carboxyl group and the terminal hydroxyl group in the ethyleneoxy spacer. A D-glucose-conjugated 15-crown-5 ether having a unique spiroketal structure was thus successfully synthesized.

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