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

Full Text (PDF, in Russian)