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
✦ LIBER ✦
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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