160195-65-3

Upstream product

• 160195-56-2 (1R,2S,3R)-2,3-isopropylidenedioxy-15-methyl-1-(thiazol-2'-yl)hexadecan-1-ol 
• 160332-84-3 (1S,2S,3R)-2,3-isopropylidenedioxy-15-methyl-1-(thiazol-2'-yl)hexadecan-1-ol 
• 160195-68-6 Methanesulfonic acid (1R,2R,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-15-methyl-hexadecyl ester 
• 160195-62-0 (2S,3S,4R)-2-azido-1,3,4-tribenzyloxy-16-methylheptadecane 
• 160195-61-9 (2R,3S,4R)-1,3,4-tribenzyloxy-16-methylheptadecan-2-ol 
• 160195-58-4 (1S,2R,3R)-2,3-isopropylidenedioxy-1-(p-methoxybenzyloxy)-15-methyl-1-(thiazol-2'-yl)hexadecane 
• 1053613-61-8 (S)-[(4R,5R)-2,2-Dimethyl-5-(12-methyl-tridecyl)-[1,3]dioxolan-4-yl]-(4-methoxy-benzyloxy)-acetaldehyde 
• 160195-59-5 (2R,3R,4R)-3,4-isopropylidenedioxy-2-(p-methoxybenzyloxy)-16-methylheptadecan-1-ol 
• 160195-67-5 (2R,3R,4R)-2-(4-Methoxy-benzyloxy)-16-methyl-heptadecane-1,3,4-triol 
• 160195-57-3 (2R,3R)-2,3-isopropylidenedioxy-15-methyl-1-(thiazol-2'-yl)hexadecan-1-one 
• 160195-50-6 2,2-Dimethyl-propionic acid (2S,3R)-2,3-dihydroxy-15-methyl-hexadecyl ester 
• 160195-55-1 (2R,3R)-2,3-isopropylidenedioxy-15-methylhexadecanal 
• 160195-54-0 (2S,3R)-2,3-isopropylidenedioxy-15-methylhexadecan-1-ol 
• 160195-49-3 (2S,3R)-15-Methyl-hexadecane-1,2,3-triol 

Relevant academic research and scientific papers

Total Synthesis of (2S,3S,4R)-2--16-methylheptadecane-1,3,4-triol 3,4-dibenzoate, a Partially Protected Ceramide Part of Sponge Cerebrosides

(2S,3S,4R)-2--16-methylheptadecane-1,3,4-triol 3,4-dibenzoate 32, apertially protected ceramide part of a cerebroside from the marine sponge Halichondria japonica, has been synthesized from L-ascorbic acid, and its absolute stereochemistry has been determined.The key steps in the synthesis include the regioselective ring opening of chiral epoxide 5 with a 2-alkyl-2-lithio-1,3-dithiane and the introduction of a hydroxymethylene synthon using Dondoni's protocol to assemble C(1) and C(2) functionality.