1267597-08-9

Upstream product

• 81470-73-7 ethyl (4R,2E)-5-(benzyloxy)-4-methylpent-2-enoate 
• 63930-49-4 (R)-3-(benzyloxy)-2-methylpropan-1-ol 
• 79026-61-2 (R)-3-benzyloxy-2-methylpropanal 
• 100-39-0 benzyl bromide 
• 126788-88-3 (R)-1-((2-methylpent-4-enyloxy)methyl)benzene 
• 63501-27-9 (2R)-2-methyl-4-penten-1-ol 

Downstream Products

• 1267597-10-3 (4R)-5-(benzyloxy)-4-methylpentanal 
• 1267597-19-2 (2R,5S,9S)-1-(benzyloxy)-9-(tert-butyldimethylsilyloxy)-2-methyldec-6-yn-5-ol 
• 1267597-21-6 [(2S,6S,9R)-10-(benzyloxy)-6-(methoxymethoxy)-9-methyldec-4-yn-2-yloxy](tert-butyl)dimethylsilane 
• 1267597-23-8 5-[(2R,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylthio]-1-phenyl-1H-tetrazole 
• 1267597-24-9 5-((2R,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole 
• 1267597-25-0 2-bromo-1-[(3'R,6'R,10'S,E)-10-tert-butyldimethylsilyloxy-6-(methoxymethoxy)-3-methylundec-1-enyl]-3,5-dimethoxybenzene 
• 1267597-26-1 methyl 2-[(3R,6R,10S,E)-10-(tert-butyldimethylsilyloxy)-6-(methoxymethoxy)-3-methylundec-1-enyl]-4,6-dimethoxybenzoate 
• 1267597-27-2 methyl 2-[(3R,6R,10S,E)-10-hydroxy-6-(methoxymethoxy)-3-methylundec-1-enyl]-4,6-dimethoxybenzoate 
• 1267597-28-3 2-[(3R,6R,10S,E)-10-hydroxy-6-(methoxymethoxy)-3-methylundec-1-enyl]-4,6-dimethoxybenzoic acid 

Relevant academic research and scientific papers

Probing the influence of an allylic methyl group in zearalenone analogues on binding to Hsp90

By the replacement of an acetate with propionate by means of organic synthesis, a range of zearalenone analogues were prepared that feature an allylic methyl group. For the synthesis of the aliphatic region of the analogues, we used an asymmetric alkylati

Biocatalytic Approach for the Total Synthesis of (-)-Malyngolide and Its C(5)-Epimer

An enzymatic approach has been successfully utilized in the total synthesis of (-)-malyngolide and its C(5)-epimer. The required configuration was established by an enzymatic kinetic resolution and Sharpless asymmetric dihydroxylation.