1198463-48-7

Upstream product

• 1198463-64-7 C₂₅H₃₄O₆ 

Downstream Products

• 1198463-38-5 (3S,4S,6R,1E)-3-(4-methoxybenzyloxy)-6-(methoxymethoxy)-1-[(2S)-4-methyl-3,6-dihydro-2H-pyran-2-yl]nona-1,8-dien-4-yl 2-[bis(2,2,2-trifluoroethoxy)phosphoryl]acetate 
• 1379586-80-7 (3S,4S,6R,1E)-3-(4-methoxybenzyloxy)-6-(methoxymethoxy)-1-[(2S)-4-methyl-3,6-dihydro-2H-pyran-2-yl]nona-1,8-dien-4-yl 4-{(2R,6R)-6-[(2S)-2-methylpent-4-ynyl]-5,6-dihydro-2H-pyran-2-yl}but-2-ynoate 
• 1198463-37-4 {(3S,4S,6R,1E)-3-(4-methoxybenzyloxy)-6-(methoxymethoxy)-1-[(2S)-4-methyl-3,6-dihydro-2H-pyran-2-yl]nona-1,8-dien-4-yl} (2Z)-4-{(2R,6R)-6-[(2S)-2-methylpent-4-ynyl]-5,6-dihydro-2H-pyran-2-yl}but-2-enoate 
• 1198463-68-1 {(3S,4S,6R,1E)-3-(4-methoxybenzyloxy)-6-(methoxymethoxy)-1-[(2S)-4-methyl-3,6-dihydro-2H-pyran-2-yl]nona-1,8-dien-4-yl} (2E)-4-{(2R,6R)-6-[(2S)-2-methylpent-4-ynyl]-5,6-dihydro-2H-pyran-2-yl}but-2-enoate 

Relevant academic research and scientific papers

Evaluating transition-metal-catalyzed transformations for the synthesis of laulimalide

(Chemical Equation Presented) Laulimalide is a structurally unique 20-membered marine macrolide displaying microtubule stabilizing activity similar to that of paclitaxel and the epothilones. The use of atom-economical transformations such as a Rh-catalyze