Synthesis of(2R, 3S)-3-amino-l,2-dihydroxyoctadecane, regioisomer of dihydrosphingosine
A. G. Tolstikov, R. Kh. Yamilov, L. V. Spirikhin, L. M. Khalilov, V. N. Odinokov, G. A. Tolstikov
Institute of Chemistry, Bashkirian Research Centre, Ural Branch, Academy of Sciences of the USSR, Ufa
Abstract: The enanthiospecific synthesis of a dihydrosphingosine regioisomer was carried out on the basis of (4R, 5R)-4,5,6-triacetoxy-2E-hexenal, a product of the acidic opening of tri-O-acetyl-D-galactal.
Russian Journal of Bioorganic Chemistry 1991, 17 (5):714-715