A Synthesis of d-erythro- and l-threo-Sphingosine and Sphinganine Diastereomers via the Biomimetic Precursor 3-Ketosphinganine
- 21 May 1998
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (12) , 3979-3985
- https://doi.org/10.1021/jo980003i
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Chemoenzymatic Synthesis of All Four Stereoisomers of Sphingosine from Chlorobenzene: Glycosphingolipid Precursors1aThe Journal of Organic Chemistry, 1998
- Conversion of dihydroceramide into ceramide: involvement of a desaturaseBiochemical Journal, 1997
- A Stereocontrolled, Convergent Synthesis of Hydroxyethylene Dipeptide IsosteresThe Journal of Organic Chemistry, 1997
- An Improved Enantiospecific Synthesis of Statine and Statine Analogs via 4-(N,N-Dibenzylamino)-3-keto EstersThe Journal of Organic Chemistry, 1997
- Effects of sphingosine stereoisomers on P-glycoprotein phosphorylation and vinblastine accumulation in multidrug-resistant MCF-7 cellsBiochemical Pharmacology, 1996
- New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis [New Synthetic Methods (85)]Angewandte Chemie International Edition in English, 1991
- Asymmetric Diels–Alder reaction with use of (S)-5-(trityloxymetyl)pyrrolidin-2-one as a chiral auxiliaryJournal of the Chemical Society, Perkin Transactions 1, 1990
- Functions of Sphingolipids and Sphingolipid Breakdown Products in Cellular RegulationScience, 1989
- A stereoselective synthesis of sphingosine, a protein kinase c inhibitor.Tetrahedron Letters, 1988
- Sphingolipid long chain basesLipids, 1970