A novel convergent strategy for the construction of oligosaccharides using TIPS-protected glycosides. Synthesis of fragments related to glycolipids of Mycobacterium smegmatis
- 27 October 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (44) , 6615-6618
- https://doi.org/10.1016/s0040-4039(00)60999-1
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Synthesis of allyl glycosides for conversion into neoglycoproteins bearing epitopes of mycobacterial glycolipid antigensCarbohydrate Research, 1992
- Lewis Acid‐Catalysed Anomerisation and Rearrangement of Alkyl D‐Glycopyranosides During Acetalisation with Methyl Pyruvate: How to Utilise it for the Preparation of 1‐(Carboxyethylidene)glycopyranosyl DonorsEuropean Journal of Organic Chemistry, 1992
- A stereoconvergent synthesis of the oligosaccharide segment of glyco- peptidolipid antigen of mycobacterium avium serotype 4 : a dominant serovariant observed in patients with acquired immune deficiency syndromeTetrahedron Letters, 1991
- [15] Mycobacterial glycolipids: Isolation, structures, antigenicity, and synthesis of neoantigensPublished by Elsevier ,1989
- Mycobacterium avium Complex Infection in Patients with the Acquired Immunodeficiency SyndromeChest, 1988
- Synthesis of the tetrasaccharide core region of antigenic lipo-oligosaccharides characteristic of mycobacterium kansasiiCarbohydrate Research, 1988
- Glycosylated trehalose. Synthesis of the oligosaccharides of the glycolipid-type antigens from Mycobacterium smegmatisCarbohydrate Research, 1987
- A convenient, one-step, high-yield replacement of an anomeric hydroxyl group by a fluorine atom using dast. Preparation of glycosyl fluorides.Tetrahedron Letters, 1985