Regioselective and stereoselective glycosylations utilizing organoboron compounds

研究成果: Short survey

1 引用 (Scopus)

抄録

Development of regio- and stereoselective glycosylations leading to a specific hydroxyl group among several free hydroxyl groups is a challenging and long-standing research subject in carbohydrate chemistry. In this context, several efficient regio- and stereoselective glycosylation methods utilizing organoboron reagents, which can bind reversibly to cis-1,2- or 1,3-diols under mild conditions, have been reported. In this focused review article, several organoboron-mediated regio- and stereoselective glycosylations are described, including recently developed methods.

元の言語English
ページ(範囲)E55-E62
ジャーナルTrends in Glycoscience and Glycotechnology
30
発行部数174
DOI
出版物ステータスPublished - 2018 1 1

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Glycosylation
Hydroxyl Radical
Research Subjects
Carbohydrates

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

これを引用

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AU - Toshima, Kazunobu

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KW - Borinic acid

KW - Boronic acid

KW - Glycosylation

KW - Organoboron compound

KW - Regioselective

KW - Stereoselective

KW - Unprotected glycoside

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