1453868-10-4

Upstream product

• 1453868-03-5 (R)-5-hydroxy-1-((4-methoxybenzyl)oxy)-2-methylpentan-3-one 
• 1453867-96-3 (R)-1-((4-methoxybenzyl)oxy)-2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-3-one 
• 212051-35-9 (R)-methyl 3-((4-methoxybenzyl)oxy)-2-methylpropanoate 
• 1453867-93-0 (R)-5-((4-methoxybenzyl)oxy)-4-methylpent-1-en-3-one 
• 449174-20-3 methyl (R)-N-methyl-N-methoxy-3-(4-methoxybenzyloxy)-2-methylpropanoate 

Downstream Products

• 1610030-08-4 C₂₂H₃₈O₄Si 
• 1610029-90-7 C₂₅H₄₄O₆SSi 
• 1610030-11-9 C₂₅H₄₄O₄SSi 
• 1610029-89-4 C₂₃H₄₀O₃SSi 
• 1610029-88-3 C₂₂H₃₆O₃SSi 
• 1610030-13-1 C₂₉H₅₀O₇SSi 
• 1610030-12-0 C₂₉H₅₂O₇SSi 

Relevant academic research and scientific papers

Total synthesis and structural revision of sekothrixide

The first total synthesis of 14-membered macrolide sekothrixide and the originally proposed structure are reported. Seven contiguous asymmetric centers in the side chain were constructed using ring-openings of several kinds of epoxide. Assembly of the lef

Stereocontrolled synthesis of 1,3-diols from enones: Cooperative lewis base-mediated intramolecular carbonyl hydrosilylations

A streamlined synthesis of β-hydroxy ketone substrates has been developed to further investigate a recently discovered cooperative Lewis base-mediated intramolecular carbonyl hydrosilylation reaction. The synthesis features an enone β-borylation/oxidation