132697-84-8Relevant articles and documents
Enantiospecific Synthesis of Sphingosine and Ceramide Stereoisomers with 3S Configuration from D-Glucose
Fujita, Shuji,Sugimoto, Mamoru,Tomita, Kenkichi,Nakahara, Yoshiaki,Ogawa, Tomoya
, p. 2561 - 2570 (2007/10/02)
Utilizing the carbon framework (C3-C6) and chirality (at C4 and C5) of D-glucose, (2S,3S,4E and 2R,3S,4E)-2-amino-4-octadecene-1,3-diol (sphingosine analogues) and four stereoisomers (2S,3S,4E-,2S,3S,4Z-,2R,3S,4E-,and 2R,3S,4Z-) of the ceramide derivatives were synthesized in a stereocontrolled way.