149157-59-5

Upstream product

• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 27784-76-5 tert-butyl diethylphosphonoacetate 
• 101712-01-0 (R)-1-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-methylpentane-1,3-dione 
• 141423-25-8 <<3-(2R,4S,5S,6R,8E),4R>-3-(5-Hydroxy-2,4,6-trimethyl-1,3-dioxo-9-phenyl-8-nonenyl)-4-(phenylmethyl)>-2-oxazolidinone 
• 149157-45-9 <2S,3S,4S,5S,6R,8E>-2,4,6-trimethyl-9-phenyl-non-8-ene-1,3,5-triol 
• 149157-55-1 <2(1S,2S,3R)>-2-ethyl-2-(1,3-dimethyl-2-((1,1-dimethylethyl)dimethylsiloxy)-formylpropyl)-1,3-dioxalane 
• 149157-57-3 1,1-dimethylethyl<2E,4S,5R,6S>-4,6-dimethyl-7-oxo-5-((1,1-dimethylethyl)dimethylsiloxy)-2-noneoate 
• 149157-54-0 <2(1S,2S,3R)>-2-ethyl-2-(1,3-dimethyl-2-((1,1-dimethylethyl)dimethylsiloxy)-4-(ethylthio)-4-oxobutyl)-1,3-dioxalane 
• 149157-56-2 1,1-dimethylethyl<2E,4S,5R,6S>-4,6-dimethyl-5-((1,1-dimethylethyl)dimethylsiloxy)-6-(2-ethyl-1,3-dioxan-2-yl)-2-hexenoate 
• 149157-46-0 <2S,4S,4(1R,2S,3R,5E),5S>-2-(4-methoxyphenyl)-5-methyl-4-(2-hydroxy-1,3-dimethyl-6-phenyl-5-hexenyl)-1,3-dioxane 
• 149157-50-6 <2R,3R,4R,5S,6R,8E>-9-iodo-2,4,6-trimethyl-5-((1,1-dimethylethyl)dimethylsiloxy)-3-((4-methoxyphenyl)methoxy)-8-nonenal 
• 149157-48-2 <2S,3S,4R,5S,6R,8E>-2,4,6-trimethyl-9-phenyl-5-((1,1-dimethylethyl)dimethylsiloxy)-3-((4-methoxyphenyl)methoxy)-1-non-8-enol 
• 149157-47-1 <2S,4S,4(1R,2S,3R,5E),5S>-2-(4-methoxyphenyl)-5-methyl-4-(1,3-dimethyl-6-phenyl-2-((1,1-dimethylethyl)dimethylsiloxy)-5-hexenyl)-1,3-dioxane 
• 149157-44-8 <3(2R,3R,4S,5S,6R,8E),4R>-3-(3,5-dihydroxy-2,4,6-trimethyl-1-oxo-9-phenyl-8-nonenyl)-4-(phenylmethyl)-2-oxazolidinone 

Downstream Products

• 92308-96-8 rutamycin B 

Relevant academic research and scientific papers

Studies directed toward the synthesis of the rutamycins. Assemblage of the polypropionate region of rutamycin B

The asymmetric synthesis of the polypropionate segment of rutamycin B is reported. In this convergent synthesis the construction of the C1-C8 and C9-C17 subunits and their union through a double stereodifferenti

Total synthesis of the macrolide antibiotic rutamycin B

A convergent asymmetric synthesis of the macrolide antibiotic rutamycin B has been achieved through the synthesis and coupling of its spiroketal and polypropionate subunits. Both fragments were constructed utilizing auxiliary based asymmetric aldol and al