Asymmetric synthesis of threo- and erythro-sphingosines by asymmetric aldol reaction of α-isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (2) , 239-240
- https://doi.org/10.1016/s0040-4039(00)80064-7
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthesis of d-erythro-sphingosinesTetrahedron Letters, 1986
- .alpha.-Amino acid derivatives as chiral educts for asymmetric products. Synthesis of sphingosine from .alpha.'-amino-.alpha.,.beta.-ynonesThe Journal of Organic Chemistry, 1986
- Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complexJournal of the American Chemical Society, 1986
- Enantioselective Synthesis of D‐erythro‐Sphingosine and of CeramideHelvetica Chimica Acta, 1986
- Useful syntheses of erythro- and threo-N-oleoyl-D-sphingosines (ceramides) and galactosylceramides (cerebrosides) from L-serineThe Journal of Organic Chemistry, 1981
- The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural ProductsSynthesis, 1981