An efficient stereocontrolled route to both enantiomers of platelet activating factor and analogs with long-chain esters at C-2: saturated and unsaturated ether glycerolipids by opening of glycidyl arenesulfonates
- 1 September 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (19) , 4643-4648
- https://doi.org/10.1021/jo00280a035
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Stereospecific synthesis of ether and thioether phospholipids. The use of L-glyceric acid as a chiral phospholipid precursorThe Journal of Organic Chemistry, 1988
- Synthesis of glycidol esters and mono/di-acylglycerols from glycidolChemistry and Physics of Lipids, 1985
- ETHER PHOSPHOLIPIDS IN GUINEA-PIG POLYMORPHONUCLEAR LEUKOCYTES AND MACROPHAGES - OCCURRENCE OF HIGH-LEVELS OF 1-ORTHO-ALKYL-2-ACYL-SN-GLYCERO-3-PHOSPHOCHOLINE1982