130052-47-0

Upstream product

• 765-09-3 1-bromotridecane 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 14618-80-5 (R)-benzyl glycidol 

Downstream Products

• 130052-43-6 (2'S)-3-O-(2'-methoxyhexadecyl)-1,2-isopropylidene-sn-glycerol 
• 130052-39-0 (S)-1-benzyloxy-2-methoxyhexadecane 
• 130052-40-3 (2'S)-1-O-(2'-methoxyhexadecyl)-3-O-benzyl-sn-glycerol 
• 130052-42-5 (S)-2-methoxyhexadecyl p-toluenesulfonate 
• 175696-45-4 C₄₇⁽¹³⁾CH₈₇NO₄Si₂ 
• 175696-47-6 C₃₈⁽¹³⁾CH₇₃NO₅Si 
• 175696-46-5 C₃₃⁽¹³⁾CH₆₅NO₃Si 
• 175696-50-1 tert-butyl [(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]carbamate 
• 175696-42-1 ((R)-1-Benzyloxymethyl-pentadecyloxy)-triisopropyl-silane 

Relevant academic research and scientific papers

Regio- and stereoselective incorporation of a13C nuclide into D-ribo-phytosphingosine via SmI2-mediated C-C formation with13C-labeled isocyanide

Preparation of a 13C-labeled isocyanide and its application to the total synthesis of [2-13C]D-ribo-C18-phytosphingosine are described. The synthesis of the labeled phytosphingosine is based on the use of the isocyanide as a 13CH-NH2 precursor in the SmI2-mediated three-component coupling reaction, wherein regio- and stereoselective incorporation of a 13C nuclide in the carbon skeleton is achieved.

Synthesis of the Stereoisomers of 1-O-(2'-Methoxyhexadecyl)glycerol and some Phosphocholine Derivatives

All four stereoisomers of 1-O-(2'-methoxyhexadecyl)glycerol have been synthesized.The stereoisomer obtained from biological material was shown to have the 2'R, 2S configuration.The corresponding phospholipid (2'R)-1-O-(2'-methoxyhexadecyl)-sn-glycero-3-ph