A New Strategy for the Synthesis of Sphingosine Analogues. Sphingofungin F
- 13 June 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (27) , 6818-6819
- https://doi.org/10.1021/ja981141s
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Catalytic Asymmetric Alkylation of Nucleophiles: Asymmetric Synthesis of α‐Alkylated Amino AcidsAngewandte Chemie International Edition in English, 1997
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995
- Acyclic Stereocontrol Induced by Allylic Alkoxy Groups. Synthetic Applications of Stereoselective Dihydroxylation in Natural Product SynthesisChemical Reviews, 1995
- Asymmetric Alkylation of Allylic gem-DicarboxylatesJournal of the American Chemical Society, 1995
- Serine Palmitoyltransferase Is the Primary Target of a Sphingosine-like Immunosuppressant, ISP-1/MyriocinBiochemical and Biophysical Research Communications, 1995
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- A modular approach for ligand design for asymmetric allylic alkylations via enantioselective palladium-catalyzed ionizationsJournal of the American Chemical Society, 1992
- Synthesis and Transannular Diels-Alder Reaction of a 13-Membered Macrocyclic Triene. A Synthetic Approach Towards the Tricyclic Part A.B.C.[6.6.5] of the Veratrum AlkaloidsSynthesis, 1992
- Simple and selective method for aldehydes (RCHO) .fwdarw. (E)-haloalkenes (RCH:CHX) conversion by means of a haloform-chromous chloride systemJournal of the American Chemical Society, 1986
- On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcoholsThe Journal of Organic Chemistry, 1986