Art

J-GLOBAL ID：200902276196473600   Reference number：05A0535027

Development of Highly Potent D-Glucosamine-Based Chiral Fluorescent Labeling Reagents and a Microwave-Assisted β-Selective Glycosidation of a Methyl Glycoside Reagent

高強力なD-グルコサミン-ベースのキラル蛍光標識試薬の開発ならびにメチルグリコシド試薬のマイクロ波関連β-選択性グリコシド化

Author (6)： OHRUI Hiroshi (Tohoku Univ., Sendai, JPN) ,  KATO Rumiko (Tohoku Univ., Sendai, JPN) ,  KODAIRA Teruhisa (Tohoku Univ., Sendai, JPN) ,  SHIMIZU Hiroki (Tohoku Univ., Sendai, JPN) ,  AKASAKA Kazuaki (Tohoku Univ., Sendai, JPN) ,  KITAHARA Takeshi (Kitasato Inst., Tokyo, JPN)
Material： Bioscience, Biotechnology, and Biochemistry  (Bioscience Biotechnology & Biochemistry)
Volume： 69  Issue： 5  Page： 1054-1057  Publication year： May. 23, 2005 
JST Material Number： G0021A  ISSN： 0916-8451  CODEN： BBBIEJ  Document type： Article
Article type： 短報  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： glycoside ,...

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JST classification (2)： Carbohydrates and sugar chains in general  (EB06010I) ,  Glycosides  (CF10057O)

Substance index (8)： N-(1-O,3-O,4-O,6-O-Tetraacetyl-2-deoxy-β-D-glucopyranose-2-yl)anthracene-2,3-dicarbimide ,  N-(1-O,3-O,4-O,6-O-Tetrabenzoyl-2-deoxy-β-D-glucopyranose-2-yl)anthracene-2,3-dicarbimide ,  N-(1-O,3-O,4-O,6-O-Tetramethyl-2-deoxy-β-D-glucopyranose-2-yl)anthracene-2,3-dicarbimide ,  1-Bromo-2-(1,3-dioxo-2,3-dihydro-1H-naphtho[2,3-f]isoindole-2-yl)-1,2-dideoxy-β-D-glucopyranose 3,4,6-triacetate ,  1-Bromo-2-(1,3-dioxo-2,3-dihydro-1H-naphtho[2,3-f]isoindole-2-yl)-1,2-dideoxy-α-D-glucopyranose 3,4,6-tribenzoate ,  1-O-(3-Methylpentyl)-2-(1,3-dioxo-2,3-dihydro-1H-naphtho[2,3-f]isoindole-2-yl)-2-deoxy-β-D-glucopyranose 3,4,6-triacetate ,  1-O-(3-Methylpentyl)-2-(1,3-dioxo-2,3-dihydro-1H-naphtho[2,3-f]isoindole-2-yl)-2-deoxy-β-D-glucopyranose 3,4,6-tribenzoate ,  1-O-(3-Methylpentyl)-2-(1,3-dioxo-2,3-dihydro-1H-naphtho[2,3-f]isoindole-2-yl)-3-O,4-O,6-O-trimethyl-2-deoxy-β-D-glucopyranose

Reference (18)：

• 1) Akasaka, K., Ohrui, H., Meguro, H., and Umetsu, T., Highly sensitive isomeric determination of beraprost sodium in plasma using a fluorescent chiral derivatization reagent. Anal. Sci., 13, 461–466 (1997).
• 2) Akasaka, K., Ohrui, H., and Meguro, H., Enantiomeric separation of carboxylic acids having chiral centers remote from the carboxyl group by labelling with a chiral fluorescent derivatization reagent. Tetrahedron Lett., 38, 6853–6856 (1997).
• 3) Akasaka, K., Imaizumi, K., and Ohrui, H., Enantiomeric separation of branched fatty acids having chiral centers remote from the carboxyl group by labelling with chiral fluorescent derivatization reagents. Enantiomer, 3, 169–174 (1998).
• 4) Akasaka, K., and Ohrui, H., Enatiomeric separation of branched fatty acids after conversion with trans-2-(2,3-anthracenedicarboximido)cyclohexanol, a highly sensitive chiral fluorescent conversion reagent. Biosci. Biotechnol. Biochem., 63, 1209–1215 (1999).
• 5) Imaizumi, K., Terashima, H., Akasaka, K., and Ohrui, H., Highly potent chiral labeling reagent for the discrimination of chiral alcohols. Anal. Sci., 19, 1243–1249 (2003).

Terms in the title (9)： D-グルコサミン ,  キラル ,  蛍光標識 ,  試薬 ,  開発 ,  メチルグリコシド ,  マイクロ波 ,  選択性 ,  グリコシド化