𝔖 Bobbio Scriptorium
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Synthesis of Analogues of the Antitumor (1→6)-Branched (1→3)-Glucohexaose

✍ Scribed by You-Lin Zeng; Jian-Jun Zhang; Fan-Zuo Kong


Book ID
102804054
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
667 KB
Volume
22
Category
Article
ISSN
0256-7660

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✦ Synopsis


Abstract

β‐D‐Glcp( 1→3)‐[β‐D‐Glcp‐( 1→6)‐/α‐D‐Manp‐( 1→3)‐β‐D‐Glcp( 1→3)‐[β‐D‐Glcp‐(1→6)‐]D‐Glcp (18) and β‐D‐Glcp( 1→3)‐[β‐D‐Glcp‐( 1→6)‐] α‐D‐Manp‐( 1→3)‐β‐D‐Glcp‐( 1 →3)‐[β‐D‐Glcp‐( 1→6)‐]β‐D‐Glcp‐D‐(1→3)‐Glcp‐1→OMe (29) were synthesized as the analogues of the immunomodulator β‐D‐Glcp‐(1→3)‐[β‐D‐Glcp‐(1→6)‐]α‐D‐Glcp‐(1→3)‐β‐D‐Glcp‐(1→3)‐(β‐D‐Glcp‐(1→6)‐]D‐Glcp through coupling of trisaccharide donors 9 with trisaccharide acceptor 16 and terrasaccharide acceptor 27 followed by deprotection. respectively.


📜 SIMILAR VOLUMES


Stereocontrolled synthesis of sulfur-lin
✍ Marie-Odile Contour-Galcera; Yili Ding; Carmen Ortiz-Mellet; Jacques Defaye 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 497 KB

The branched, sulfur-linked tetrasaccharide S-(beta-D-glucopyranosyl)-(1-->3)-S-[(6-S-beta-D-glucopyranosyl)-3,6-dit hio- beta-D-glucopyranosyl]-(1-->3)-S-3-thio-D-glucopyranose (9) has been conveniently prepared by SN2 displacement of the triflate group in 1,2:5,6-di-O-isopropylidene-3-O-trifluorom