Trityl ethers in oligosaccharide synthesis: A novel strategy for the convergent assembly of oligosaccharides

Tetrahedron Letters

Volumn 38, Issue 21, 1997, Pages 3773-3776

  Boons, Geert Jan ^a   Bowers, Simeon ^a   Coe, Diane M ^b  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b GLAXOSMITHKLINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

OLIGOSACCHARIDE;

ARTICLE; CARBOHYDRATE SYNTHESIS; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS;

EID: 0030915322     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00732-6     Document Type: Article

References (13)

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8. It has been reported that the steric effects of a bulky 6-substituent effect the α-selectivivty of glycosylations of thioglycosides. However, in this study IDCP was used as a promotor and inferior yields were obtained. S. Houdier, P.J.A. Vottero, Carbohydr. Res., 1992, 252, 349.
9. G.H. Veeneman, S. H. van Leeuwen, J.H. van Boom, Tetrahedron Lett., 1990, 31, 1331
10. 13C NMR and high resolution MS data.
11. a) G.J. Boons, P. Grice, R. Leslie, S.V. Ley, L.L. Yeung, Tetrahedron Lett., 1993, 34, 8523;
12. b) S.V. Ley, H.W.M. Priepke, Angew. Chem. Int. Ed. Engl., 1994, 33, 2292;
13. c) G.J. Boons, R. Geurtsen, D. Holmes, Tetrahedron Lett., 1995, 36, 6325.