✦ LIBER ✦

Design and Synthesis of C 3 -Symmetric Lewis X Antigen

✍ Scribed by Nishida, Yoshihiro; Tsurumi, Tomoaki; Sasaki, Kenji; Watanabe, Kenta; Dohi, Hirofumi; Kobayashi, Kazukiyo

Book ID: 127043168
Publisher: American Chemical Society
Year: 2003
Tongue: English
Weight: 123 KB
Volume: 5
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol0351293

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Design and Synthesis of C3-Symmetric Lew

Design and Synthesis of C3-Symmetric Lewisx Antigen.

✍ Yoshihiro Nishida; Tomoaki Tsurumi; Kenji Sasaki; Kenta Watanabe; Hirofumi Dohi; 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 52 KB

Design and Synthesis of Sialyl Lewis X M

Design and Synthesis of Sialyl Lewis X Mimetics

✍ Uchiyama, Taketo; Vassilev, Vassil P.; Kajimoto, Tetsuya; Wong, Weichyun; Lin, C 📂 Article 📅 1995 🏛 American Chemical Society 🌐 English ⚖ 240 KB

Chemoenzymatic synthesis of GM3, Lewis x

Chemoenzymatic synthesis of GM3, Lewis x and sialyl Lewis x oligosaccharides in 13C-enriched form

✍ Mark A. Probert; Mark.J. Milton; Richard Harris; Sergio Schenkman; Jonathan M. B 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 251 KB

In connection with studies on the solution and protein-bound conformation of oligosaecharides, we had reason to consider the application of 13C-enriched sugars. Herein we describe the synthesis of ganglioside GM3 trisaccharide (1), Lewis x trisaccharide (2) and the sialyl Lewis x tetrasaccharide (3)

Design and synthesis of novel sialyl Lew

Design and synthesis of novel sialyl Lewis x mimics

✍ Neelu Kaila; Hsiang-Ai Yu; YiBin Xiang 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 224 KB

Efficient synthesis of lactoneo series a

Efficient synthesis of lactoneo series antigens H, Lewis X (Lex), and Lewis Y (Ley)1

✍ Rainer Windmüller; Richard R. Schmidt 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 253 KB

A versatile synthesis of the lactoneo-se

A versatile synthesis of the lactoneo-series antigens — synthesis of sialyl dimer Lewis X and of dimer Lewis Y

✍ Gerd Hummel; Richard R Schmidt 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 254 KB

Readily available fucosyl ct(l-3)azidoglucose disaccharide 6 is transformed with galactosyl donors 7 and 8 into Lewis X trisacchadde building blocks 9 and 12, respectively, in high yield. Their suitability for the construction of the lactoneo-series glycosphingolipids is demonstrated. For instance,