1446944-33-7

Upstream product

• 100-39-0 benzyl bromide 
• 5949-05-3 (S)-Citronellal 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 220272-08-2 (4S)-6-(benzyloxy)-4-methylhexan-1-ol 
• 138604-47-4 (S)-6-benzyloxy-4-methylhexanal 
• 84237-05-8 (S)-((3,7-dimethyloct-6-enyloxy)methyl)benzene 
• 67245-14-1 (3S,6RS)-1-benzyloxy-6,7-epoxy-3,7-dimethyloctane 

Downstream Products

• 1446944-75-7 (3S,11R)-1-benzyloxy-3,11,15-trimethyl-14-hexadecen-7-yne 
• 1446944-54-2 (3S,11S)-3,11-dimethylpentadecyl tosylate 
• 1446944-90-6 (3S,11R)-3,11-dimethylpentadecyl tosylate 
• 130797-63-6 (S)-3-Methylpentadecyl tosylate 
• 1446944-78-0 (3S,11S,14RS)-1-benzyloxy-14,15-epoxy-3,11,15-trimethyl-7-hexadecyne 
• 1446944-50-8 (3S,11R,14RS)-1-benzyloxy-14,15-epoxy-3,11,15-trimethyl-7-hexadecyne 
• 1446944-51-9 (4R,12S)-14-benzyloxy-4,12-dimethyl-7-tetradecynal 
• 1446944-81-5 (4S,12S)-14-benzyloxy-4,12-dimethyl-7-tetradecynal 
• 1446944-52-0 (3S,11S)-1-benzyloxy-3,11-dimethyl-14-pentadecen-7-yne 
• 1446944-84-8 (3S,11R)-1-benzyloxy-3,11-dimethyl-14-pentadecen-7-yne 
• 1446944-34-8 (S)-1-benzyloxy-3-methyl-7-pentadecyne 
• 1446944-49-5 (3S,11S)-1-benzyloxy-3,11,15-trimethyl-14-hexadecen-7-yne 

Relevant academic research and scientific papers

Synthesis of a comprehensive polyprenol library for the evaluation of bacterial enzyme lipid substrate specificity

Polyprenols, a universal class of glycan-carrier lipids, play important roles in glycan biosynthesis in wide variety of living organisms. The chemical synthesis of natural polyisoprenols such as undecaprenol and dolichols, and even more so the synthesis o

Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal

The enantiomers of citronellal were converted to all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2- octadecanone, the female-produced sex pheromone components of the Lyclene dharma dharma moth. Three wellestablished procedures, the Wittig reaction, alkylation of alkynes, and acetoacetic ester synthesis, were employed for the carbon-carbon bond formation to connect the building blocks.