An efficient and highly stereoselective α(1→4) glycosylation between two d-galacturonic acid ester derivatives
- 1 January 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (2) , 241-244
- https://doi.org/10.1016/s0040-4039(96)02308-8
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Synthesis of methyl esters of 3-deoxy- d - erythro -2-hexulosonic acid (KDG) analogs, inducers of the expression of pectinase genes in bacteria Erwinia chrysanthemiTetrahedron, 1996
- Synthesis and Polycondensation ofGalacto-Configurated MonomersViathe Trityl-cyano-ethylidene-ProcedureJournal of Carbohydrate Chemistry, 1994
- d-Galacturonic acid derivatives as acceptors and donorsin glycosylation reactionsCarbohydrate Research, 1992
- Stereoselective total synthesis of dodecagalacturonic acid, a phytoalexin elicitor of soybeanCarbohydrate Research, 1990
- Recent developments in the synthesis of glycoconjugatesPublished by Walter de Gruyter GmbH ,1989
- Synthesis of methyl (allyl 2,3-di-O-benzyl-β-d-galactopyranosid)uronate and methyl (2,3-di-O-benzyl-α- and β-d-galactopyranosyl fluoride)uronateCarbohydrate Research, 1988
- Tetrahedron report number 218Tetrahedron, 1987
- A highly efficient, practical, and stereoselective approach to the synthesis of α 1→4 linked galactooligosaccharidesTetrahedron Letters, 1987
- Synthesis of a disaccharide component of the capsular polysaccharide antigen of Streptococcus pneumoniae type 1Carbohydrate Research, 1984
- AN EFFICIENT METHOD FOR GLUCOSYLATION OF HYDROXY COMPOUNDS USING GLUCOPYRANOSYL FLUORIDEChemistry Letters, 1981