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Ring-Opening Polymerization of a 1,4-Anhydro Xylose Derivative Having an Azido Group and Synthesis of Stereoregular 3-Amino-3-deoxy-(1→5)-α- d -xylofuranan

✍ Scribed by Yoshida, Takashi; Kang, Byongwon; Hattori, Kazuyuki; Qing, Huang; Uryu, Toshiyuki

Book ID
126407169
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
247 KB
Volume
29
Category
Article
ISSN
0024-9297

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📜 SIMILAR VOLUMES

Synthesis of 3-amino-ribofuranans having
Synthesis of 3-amino-ribofuranans having 1,5-α and -β structures by selective ring-opening polymerization of a 1,4-anhydro-3-azido-3-deoxy-α-D-ribopyranose derivative
✍ Byoung Won Kang; Kazuyuki Hattori; Takashi Yoshida; Makoto Hirai; Yoon Soung Chi 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 648 KB

## Abstract Ring‐opening polymerization of a new anhydro ribose‐type monomer, 1,4‐anhydro‐3‐azido‐3‐deoxy‐2‐__O‐tert__‐butyldimethylsilyl‐α‐D‐ribopyranose (A3ASR), was investigated. The monomer was synthesized from 1,4‐anhyro‐α‐D‐xylopyranose by three steps comprising Walden inversion at the C3 pos

Ring-opening polymerization and copolyme
Ring-opening polymerization and copolymerization of a new benzylated 1,6-anhydro-3-azido-3-deoxy-β-D-allopyranose and synthesis of amino-polysaccharides with 1,6-α-allopyranosidic structure
✍ Kazuyuki Hattori; Takashi Yoshida; Toshiyuki Uryu 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 548 KB

## Abstract Ring‐opening polymerization of a new anhydro‐hexose monomer having an azido group, 1,6‐anhydro‐3‐azido‐2,4‐di‐__O__‐benzyl‐3‐deoxy‐β‐D‐allopyranose (A3ABA), was carried out with Lewis acid catalysts to give a stereoregular (1→6)‐α‐D‐allopyranan derivative having the azido group at the C