Diastereoselective synthesis of N-acetyl-,-acosamine and N-benzoyl-,-ristosamine
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (34) , 4133-4136
- https://doi.org/10.1016/s0040-4039(00)89312-0
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Carbamate-mediated functionalization of unsaturated alcohols. 3. Intramolecular Michael addition of O-carbamates to .alpha.,.beta.-unsaturated esters. A new diastereoselective amination in an acyclic systemJournal of the American Chemical Society, 1985
- A new synthesis of N-benzoyl L-acosamineTetrahedron Letters, 1984
- Acyclic stereoselection. 19. Total synthesis of (±)-ristosamine and (±)-megalosamine.Tetrahedron Letters, 1983
- Synthesen biologisch wichtiger Kohlenhydrate, 13: Synthese des N ‐Acetyl‐ L ‐acosamins (3‐Acetylamino‐2,3,6‐tridesoxy‐ L ‐ arabino ‐hexose)European Journal of Inorganic Chemistry, 1978