149157-52-8

Upstream product

• 93622-24-3 2-ethyl-2-ethoxy-1,3-dioxalane 
• 101712-01-0 (R)-1-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-methylpentane-1,3-dione 
• 149157-51-7 (3(2R,4R),4R)-3-[2,4-dimethyl-1,3-dioxo-4-(2-ethyl-1,3-dioxan-2-yl)butyl]-4-(phenylmethyl)-2-oxazolidinone 

Downstream Products

• 149157-58-4 1,1-dimethylethyl<2E,4S,5R,6S,8R,9S,10S,11S,12R,13S,14R,16E>-9-hydroxy-17-iodo-4,6,8,10,12,14-hexamethyl-7-oxo-11-((4-methoxyphenyl)methoxy)-5,13-bis((1,1-dimethylethyl)dimethylsiloxy)heptadeca-2,16-dienoate 
• 149157-59-5 1,1-dimethylethyl<2E,4S,5R,6S,8R,9S,10R,11R,12R,13S,14R,16E>-17-iodo-4,6,8,10,12,14-hexamethyl-7-oxo-11-((4-methoxyphenyl)methoxy)-5,9,13-tris((1,1-dimethylethyl)dimethylsiloxy)heptadeca-2,16-dienoate 
• 92308-96-8 rutamycin B 
• 149157-53-9 <3(2R,3S,4S),4R>-3-(2,4-dimethyl-1-oxo-3-((,1-dimethylethyl)dimethylsiloxy)-4-(2-ethyl-1,3-dioxan-2-yl)butyl)-4-(phenylmethyl)-2-oxazolidinone 

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