Art

J-GLOBAL ID：201602215209310372   Reference number：16A0497734

Efficient Synthesis of the Lewis A Tandem Repeat

LewisAタンデム繰り返しの効率的合成

Author (12)： KOBAYASHI Daisuke (Gifu Univ., Gifu, JPN) ,  UEKI Akiharu (Gifu Univ., Gifu, JPN) ,  UEKI Akiharu (Kyoto Univ., Kyoto, JPN) ,  UEKI Akiharu (Aomori Univ., Aomori, JPN) ,  YAMAJI Tomoya (Gifu Univ., Gifu, JPN) ,  NAGAO Kazuya (Gifu Univ., Gifu, JPN) ,  IMAMURA Akihiro (Gifu Univ., Gifu, JPN) ,  ANDO Hiromune (Gifu Univ., Gifu, JPN) ,  ANDO Hiromune (Kyoto Univ., Kyoto, JPN) ,  KISO Makoto (Gifu Univ., Gifu, JPN) ,  KISO Makoto (Kyoto Univ., Kyoto, JPN) ,  ISHIDA Hideharu (Gifu Univ., Gifu, JPN)
Material： Molecules (Web)
Volume： 21  Issue： 5  Page： WEB ONLY  Publication year： May. 2016 
JST Material Number： U7014A  ISSN： 1420-3049  CODEN： MOLEFW  Document type： Article
Article type： 原著論文  Country of issue： Switzerland (CHE)  Language： ENGLISH (EN)

Thesaurus term： *surface antigen ,  *carbohydrate chain ,  glycoprotein ,  antitumor action ,  glycosylation ,  *chemical synthesis ,  *oligosaccharide ,  nitrile ,  donor-acceptor pair
Semi thesaurus term： *Lewis antigen ,  galactosylation ,  fucosylation ,  *stereoselective synthesis

JST classification (3)： Addition reaction,elimination reaction  (CF02030M) ,  Oligosaccharides  (CF10053Y) ,  Proteins and peptides in general  (EB03010N)

Substance index (5)： Phenyl 3-O-allyl-2-O,4-O,6-O-tribenzyl-1-thio-β-D-galactopyranoside ,  tert-Butyldiphenylsilyl 4-O,6-O-benzylidene-2-azido-2-deoxy-β-D-glucopyranoside ,  tert-Butyldiphenylsilyl 3-O-(3-O-allyl-2-O,4-O,6-O-tribenzyl-β-D-galactopyranosyl)-6-O-benzyl-2-(trichloroacetylamino)-2-deoxy-β-D-glucopyranoside ,  N-Phenyl-2,2,2-trifluoroacetimidic acid 3-O,4-O-diacetyl-2-O-(4-methoxybenzyl)-L-fucopyranosyl ester ,  tert-Butyldiphenylsilyl 4-O-(2-O,3-O,4-O-triacetyl-α-L-fucopyranosyl)-3-O-(3-O-allyl-2-O,4-O,6-O-tribenzyl-β-D-galactopyranosyl)-6-O-benzyl-2-(trichloroacetylamino)-2-deoxy-β-D-glucopyranoside

Terms in the title (1)： タンデム