136537-06-9Relevant academic research and scientific papers
Ozonolyses of enantiopure 4-alkoxy-3,6-dihydro-2H-1,2-oxazines: An expedient route to functionalized α-amino-β-hydroxy esters
Helms, Matthias,Reissig, Hans-Ulrich
, p. 998 - 1001 (2007/10/03)
Ozonolysis and subsequent in situ acylation/base treatment converted the enantiopure carbohydrate-derived 1,2-oxazines 1, 5, 8 (either syn- or anti-configured) and anti-11 into the highly functionalized α-amino- β-hydroxy esters 2, 6, 9 and 12 in moderate
Synthesis of Sphingosine Relatives, XI: Synthesis of Wheat Grain Cerebroside with Fruiting-Inducing Effect on Schizophyllum commune
Mori, Kenji,Kinsho, Takeshi
, p. 1309 - 1316 (2007/10/02)
(2S,3R,8Z)-1-O-(β-D-Glucopyranosyl)-N-hexadecanoyl-8-sphingenine (1) and its (8E) isomer 1(E) were synthesized by starting from D-(-)-tartaric acid.Key Words: Cerebroside / Sphingosine, dihydro / Tartaric acid
