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Synthesis of Muropeptide Conjugates of 2,3-Dideoxy-β-D-manno-2-octulosonic Acid

✍ Scribed by Dr. Hans-Georg Lerchen; Dr. Hein-Peter Kroll


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
310 KB
Volume
30
Category
Article
ISSN
0044-8249

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✦ Synopsis


benzyl ether function to give the deprotected heptasaccharide 19 [yield 93.5%, [ I &' -19" (c = 0.69, H,O); Lit. [3b]: [a];' -12" (C = 0.5, H20)].


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✍ Nico Bräuer; Andreas Kirschning; Ernst Schaumann 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 115 KB 👁 2 views

KDO (1) is synthesized in five steps, starting from 1,2-to the carbonate 9. Silicon-induced lactonization affords the lactone 10, which can be converted into NH 4 -KDO by anhydro-3,4:5,6-di-O-isopropylidene-D-mannitol ( 6). The epoxide 6, obtained from D-mannitol (2), reacts with lithiated standard