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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
openaire +1 more source
Stereospecific synthesis of D-threo-sphinganine
The Journal of Organic Chemistry, 1974openaire +1 more source
Biosynthesis of sphingolipids: Dihydroceramide and not sphinganine is desaturated by cultured cells
Biochemical and Biophysical Research Communications, 1992Konrad Sandhoff
exaly