An efficient glycosidation method using 2,3-unsaturated glycosyl donors

Kaname Sasaki, Shuichi Matsumura, Kazunobu Toshima

研究成果: Article査読

14 被引用数 (Scopus)

抄録

A novel class of 'armed' glycosyl donors containing a double bond at the C-2 position was designed by mimicking the mechanism of lysozyme-initiated hydrolysis. These donors were used to achieve chemoselective glycosidation of hex-2-enopyranosyl acetate and hexopyranosyl acetate, and synthesis of O-glycosidic linkages between highly deoxygenated sugars and tertiary alcohols.

本文言語English
ページ(範囲)9039-9043
ページ数5
ジャーナルTetrahedron Letters
47
51
DOI
出版ステータスPublished - 2006 12 18

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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