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Synthesis of the α and β anomer of an N-triglycosyl dipeptide

✍ Scribed by Tadahiro Takeda; Atsushi Utsuno; Naoki Okamoto; Yukio Ogihara; Seiichi Shibata


Book ID
102991338
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
681 KB
Volume
207
Category
Article
ISSN
0008-6215

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✦ Synopsis


O-alpha-D-Glucopyranosyl-(1----6)-O-beta-D-glucopyranosyl-(1----6)-1-N- [L-aspart-1-oyl-(L-proline)-4-oyl]-alpha- and -beta-D-glucopyranosylamine have been prepared, as models for a derivative possibly present in the glomerular basement membrane of rats, by condensation of the corresponding D-glucosyl-dipeptide derivatives with 2,3,4,2',3',4',6'-hepta-O-acetyl-alpha-D-isomaltopyranosyl bromide in the presence of mercuric cyanide, followed by deprotection of the trisaccharide-dipeptide derivatives.


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Synthesis of α and β anomers of UDP-N-ac
✍ Didier Blanot; Geneviève Auger; Dominique Liger; Jean van Heijenoort 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 617 KB

A convenient synthesis of UDP-N-acetylmuramic acid, a key compound for the study of the cytoplasmic synthetases of bacterial peptidoglycan, is described. Separation of its two anomers was carried out by HPLC. The a anomer is identical with natural UDP-N-acetylmuramic acid. Both anomers are substrate