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Synthesis of sphinganine analogues modified in the head group
Tetrahedron, 1994Abstract The synthesis of sphinganine analogues modified in the head group is reported. The target compounds are efficiently prepared by means of the Henry reaction. Synthesis and results of preliminary investigations of the derivatives as potential inhibitors of sphingolipid biosynthesis are presented.
Thomas Kolter +2 more
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ChemInform Abstract: Synthesis of Phosphoramide Analogues of Sphinganine‐1‐phosphate.
ChemInform, 1996AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
A. SCHICK +3 more
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Chemischer Informationsdienst, 1986
AbstractThe trichloroacetimidate (V) ‐ obtained from the protected propynol (I) ‐ undergoes iodocyclization to give the dihydrooxazole (VI).
A. BONGINI +4 more
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AbstractThe trichloroacetimidate (V) ‐ obtained from the protected propynol (I) ‐ undergoes iodocyclization to give the dihydrooxazole (VI).
A. BONGINI +4 more
openaire +1 more source
Asymmetric synthesis of sphinganine and ent-clavaminol [corrected] H.
The Journal of organic chemistry, 2010An efficient enantioselective synthesis of sphinganine and ent-clavaminol [corrected] H is reported. These sphingoid-type bases were obtained from commercially available fatty acids using highly enantioselective Ru-catalyzed hydrogenation and organocatalytic electrophilic amination reactions to create the stereogenic centers.
Ramzi, Ait-Youcef +2 more
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Stereospecific synthesis of D-threo-sphinganine
The Journal of Organic Chemistry, 1974openaire +1 more source