Synthesis of two pairs of enantiomeric C18-sphingosines
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (51) , 7205-7208
- https://doi.org/10.1016/s0040-4039(01)93935-8
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Structural requirements for long-chain (sphingoid) base inhibition of protein kinase C in vitro and for the cellular effects of these compoundsBiochemistry, 1989
- Asymmetric synthesis of threo- and erythro-sphingosines by asymmetric aldol reaction of α-isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complexTetrahedron Letters, 1988
- A stereoselective synthesis of sphingosine, a protein kinase c inhibitor.Tetrahedron Letters, 1988
- Fumarase-catalyzed synthesis of L-threo-chloromalic acid and its conversion to 2-deoxy-D-ribose and D-erythro-sphingosineThe Journal of Organic Chemistry, 1987
- .alpha.-Amino acid derivatives as chiral educts for asymmetric products. Synthesis of sphingosine from .alpha.'-amino-.alpha.,.beta.-ynonesThe Journal of Organic Chemistry, 1986
- Enantioselective Synthesis of D‐erythro‐Sphingosine and of CeramideHelvetica Chimica Acta, 1986
- AN EFFICIENT SYNTHESIS OF (2S,3R)- AND (2S,3S)-SPHINGOSINEChemistry Letters, 1985
- Useful syntheses of erythro- and threo-N-oleoyl-D-sphingosines (ceramides) and galactosylceramides (cerebrosides) from L-serineThe Journal of Organic Chemistry, 1981
- Stereoselective synthesis of D-erythro-sphingosineJournal of the American Chemical Society, 1973
- Synthesis of trans- and cis-SphingosineThe Journal of Organic Chemistry, 1970