260449-38-5

Upstream product

• 22089-60-7 benzyl prenyl ether 
• 260449-37-4 (2R,3R)-2-(tert-butyldimethylsilanyloxy)-3,4-dimethylpent-4-en-1-ol 
• 260449-36-3 (R)-4-((R)-1,2-Dimethyl-allyl)-2,2-dimethyl-[1,3]dioxolane 
• 260449-30-7 (2S,3R)-3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-butan-2-ol 
• 191410-59-0 (2R,3R,4S)-1-benzyloxy-3-methyl-2,4-pentanediol 
• 191151-22-1 (S)-1-((2S,3S)-3-Benzyloxymethyl-2-methyl-oxiranyl)-ethanol 
• 101376-74-3 (E)-4-(benzyloxy)-2-methylbut-2-enal 

Relevant academic research and scientific papers

Synthetic studies toward potent cytotoxic agents amphidinolides: Synthesis of the C1-C6 and C9-C17 moieties of amphidinolides O and P

Stereoselective synthesis of the (4R)-C1-C6 and (14R, 15R)-C9-C17 segments, 4 and 5 respectively, of amphidinolides O and P have been achieved starting from a common chiral precursor 6 which was obtained by radical-mediated opening of a trisubstituted epoxy alcohol using Cp2TiCl-cyclohexa-1,4-diene.