Zaragozic acid: Unusual stereochemical dependence in anhydride formation of carbohydrate templates
- 13 March 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (11) , 1933-1936
- https://doi.org/10.1016/0040-4039(95)00160-e
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Synthetic studies towards the squalestatins and zaragozic acidsTetrahedron Letters, 1994
- Zaragozic acid a : Interesting observations in anhydro-ring formation of densely functionalised carbohydrate templatesTetrahedron Letters, 1994
- The first synthesis of the novel 2,8-dioxabicyclo[3.2.1]octane ring system: a key feature of the squalestatinsJournal of the Chemical Society, Chemical Communications, 1994
- The zaragozic acids: Structure elucidation of a new class of squalene synthase inhibitorsTetrahedron Letters, 1993
- Synthesis of the bicyclic core structure of squalestatin 1Journal of the Chemical Society, Chemical Communications, 1993
- Zaragozic acid A, a potent inhibitor of squalene synthase: initial chemistry and absolute stereochemistryThe Journal of Organic Chemistry, 1992
- On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical ruleTetrahedron, 1984
- 4'-Substituted nucleosides. 5. Hydroxymethylation of nucleoside 5'-aldehydesThe Journal of Organic Chemistry, 1979