1616376-35-2

Upstream product

• 75-16-1 methylmagnesium bromide 
• 1616376-28-3 C₁₃H₁₇F₃O₅S 
• 160238-45-9 (2S)-3-(4-methoxybenzyloxy)-2-methyl-1-propanol 
• 212051-35-9 (R)-methyl 3-((4-methoxybenzyl)oxy)-2-methylpropanoate 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 765915-17-1 (2R,4S)-5-((4-methoxybenzyl)oxy)-2,4-dimethylpentan-1-ol 
• 1616376-34-1 (4S)-4-benzyl-3-((2R,4S)-5-((4-methoxybenzyl)oxy)-2,4-dimethylpentanoyl)oxazolidin-2-one 

Downstream Products

• 1616376-36-3 (4R)-4-benzyl-3-((2S,4S,6S)-2,4,6-trimethyloctanoyl)oxazolidin-2-one 
• 1616376-50-1 (2R)-methyl 2-phenyl-2-((2S,4S,6S)-2,4,6-trimethyloctanamido)acetate 
• 1616376-51-2 (2S)-methyl 2-phenyl-2-((2S,4S,6S)-2,4,6-trimethyloctanamido)-acetate 

Relevant academic research and scientific papers

Prediction and determination of the stereochemistry of the 1,3,5-trimethyl-substituted alkyl chain in verucopeptin, a microbial metabolite

For the prediction of the relative stereochemistry of 1,3-dimethyl substitution in alkyl chains, a simple approach based on 1H NMR data was recently proposed; Δδ values of methylene protons located between methyl-substituted methine carbons can