The synthesis of 4-deoxy-L-glycero-pentulose by biochemical dehydrogenation of 2-deoxy-D-erythro-pentitol
✍ Scribed by Kazimír Linek; Rozália Sandtnerová; Tibor Sticzay; Vladimír Kovác̆ik; Milos̆ Kulhánek; Milan Tadra
- Book ID
- 102639327
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 367 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0008-6215
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## Abstract For Abstract see ChemInform Abstract in Full Text.
The title compounds, required for the identification of structural features of the Bordetella pertussis endotoxin, have been synthesised by condensation of benzyl 3-O-benzyl-2-deoxy-beta-L-erythro-pentopyranoside with 2,3,4,6-tetra-O-benzoyl-alpha-D-mannopyranosyl bromide and with 4,6-di-O-acetyl-2,
A study aimed at developing an enantioselective synthesis of the title compound 23, a 2-monodeoxy analogue of the naturally occurring ()-2-keto-3-deoxy-d-glycero-d-galacto-2-nononic acid (KDN), is reported. From d-mannose as starting material, the chiral 1,3-diene 10, activated by a silyloxy substit