Stereocontrolled, total synthesis of α-d-GalA-[1→4)-α-d-GalA]8-(1→4)-β-d-GalA-1→OPr, a synthetic model for phytoalexin elicitor-active oligogalacturonic acids
- 15 September 1987
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 167, C1-C7
- https://doi.org/10.1016/0008-6215(87)80292-6
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- A highly efficient, practical, and stereoselective approach to the synthesis of α 1→4 linked galactooligosaccharidesTetrahedron Letters, 1987
- Host-Pathogen InteractionsPlant Physiology, 1986
- Cell Surfaces in Plant-Microorganism InteractionsPlant Physiology, 1985
- Phytoalexins and their Elicitors-A Defense Against Microbial Infection in PlantsAnnual Review of Plant Physiology, 1984
- STRUCTURE AND FUNCTION OF THE PRIMARY CELL WALLS OF PLANTSAnnual Review of Biochemistry, 1984
- Characteristics of Galacturonic Acid Oligomers as Elicitors of Casbene Synthetase Activity in Castor Bean SeedlingsPlant Physiology, 1984
- Host-Pathogen InteractionsPlant Physiology, 1984
- Host-Pathogen InteractionsPlant Physiology, 1983
- Host-Pathogen InteractionsPlant Physiology, 1981
- Proteinase inhibitor-inducing factor activity in tomato leaves resides in oligosaccharides enzymically released from cell wallsProceedings of the National Academy of Sciences, 1981