1385634-72-9

Upstream product

• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 343221-33-0 6-((4-methoxybenzyl)oxy)hexanoic acid 
• 33467-04-8 (4S,6S)-4-tert-butyl-6-methyl-2-oxo-1,3,2-dioxathiane 
• 1385634-52-5 C₁₂H₂₄O₃ 
• 1385634-51-4 C₁₂H₂₄O₂ 
• 1385634-50-3 (5S,7S)-5,8,8-trimethylnonane-1,7-diol 
• 1385634-49-0 (3S,5S)-9-(benzyloxy)-2,2,5-trimethylnonan-3-ol 
• 1385634-53-6 (5S,7S)-7-hydroxy-N,5,8,8-tetramethylnonanamide 
• 1385634-65-0 (S)-6-((4-methoxybenzyl)oxy)-2-methylhexanoic acid 
• 1385634-64-9 N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl) (2R)-6-((4-methoxybenzyl)oxy)-N,2-dimethylhexanamide 
• 1385634-63-8 N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-((4-methoxybenzyl)oxy)-N-methylhexanamide 

Relevant academic research and scientific papers

Evolution of a protecting-group-free total synthesis: Studies en route to the neuroactive marine macrolide (-)-palmyrolide A

A full account of our synthetic work toward the first total synthesis of the neuroactive marine macrolide (-)-palmyrolide A is described. Our first-generation approach aimed to unlock the unknown C(5)-C(7) stereochemical relationship via the synthesis of