Synthesis of 2,4-dideoxy-d-erythro-hexopyranose. An intermediate for synthesis of the lactone moiety of inhibitors of hydroxymethylglutaryl-coenzyme A reductase
- 15 February 1984
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 125 (2) , 318-322
- https://doi.org/10.1016/0008-6215(84)85167-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Mevinic acids and analogues: preparation of a key chiral intermediateTetrahedron Letters, 1982
- Methyl 3-0-benzyl-2,4,6-trideoxy-6-iodo-α-d--hexopyranoside, a chiral synthon for the synthesis of inhibitors of HMG-CoA reductaseTetrahedron Letters, 1982
- Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent.Proceedings of the National Academy of Sciences, 1980
- Therapeutic effects of ML-236B in primary hypercholesterolemiaAtherosclerosis, 1980
- Umpolung of the Reactivity of Carbonyl Compounds Through Sulfur-Containing ReagentsSynthesis, 1977
- Rules for ring closureJournal of the Chemical Society, Chemical Communications, 1976
- A new method for the deoxygenation of secondary alcoholsJournal of the Chemical Society, Perkin Transactions 1, 1975
- 528. Phosphorylated sugars. Part X. A simple synthesis of 3-deoxy-D-erythro-pentose 5-(dihydrogen phosphate)Journal of the Chemical Society, 1965