𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Crystal structure of 2-deoxy-β-darabino-hexose (2-deoxy-β-d-glucose)

✍ Scribed by Raffaella Puliti; Carlo A. Mattia; Guido Barone


Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
313 KB
Volume
182
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

✦ Synopsis


Isfituto per la Chimica di Mofecofe o'i Wexsse

Bi5iogic5 del C. N. R., viu T&am 6, E10072 Arm Fe f f ce, Napo fi (If a/y


📜 SIMILAR VOLUMES


Crystal structure of 2-deoxy-β-d-lyxo-he
✍ Raffaella Puliti; Carlo A. Mattia; Guido Barone 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 344 KB

2-Deoxy-P-D-lyxo-hexose (2-deoxy+-D-galactose, C,H,,O,), M, = 164.16, is monoclinic, P2, with a = 9.811(l), b = 6.953(l), c = 5.315(l) A, p = 91.58(2)", V = 362.5(l) A3, Z = 2, and D, = 1.504 g.cme3. The structure was solved by direct methods (MULTAN 79) and refined to R = 0.032 for 800 observed ref

Preparation of 2-deoxy-β-d-lyxo-hexoside
✍ David Crich; Timothy J. Ritchie 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 211 KB

With a view to the eventual synthesis of the trisaccharide chain of the antitumor antibiotic olivomycin A1 (1)) we have studied the preparation2 of heptulosonic acid 0-glycosides and their stereoselective radical decarboxylation3 to 2-deoxy-EDarubino-hexosides (2deoxy-/3-D-glucosides). We now report

Methyl 3-amino-3-deoxy-β-d-galactopyrano
✍ Anne-Charlotte Helland; Ole Hindsgaul; Monica M. Palcic; Cheryl L.M. Stults; Bru 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 422 KB

UDP-D-galactose:fl-D-galactopyranosyl-(l ~ 4)-2-acetamido-2-deoxy-D-glucose a-(1 ~ 3)-Dgalactopyranosyltransferase [E.C . 2.4.1.151] transfers o-galactosyl-residues from the sugar nucleotide with retention of configuration. We report here that synthetic methyl 3'-amino-3'-deoxy-N-acetyllactosaminide

Syntheses of β-C(1→3)-Glucopyranosides o
✍ Raynald Demange; Carine Bühlmann; Pierre Vogel 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 260 KB

## Abstract The __OshimaNozaki__ (Et~2~AlI) condensation of isolevoglucosenone (**4**) with 2,6‐anhydro‐3,4,5,7‐tetra‐__O__‐benzyl‐D‐__glycero‐__D‐__gulo__‐heptose (**5**) gave an enone **6** that was converted with high stereoselectivity to 3‐__C__‐[(1__R__)‐2,6‐anhydro‐D‐__glycero‐__D‐__gulo__‐h