1448848-24-5

Upstream product

• 3929-47-3 3-(3,4-dimethoxyphenyl)-1-propanol 
• 61871-67-8 3-(3,4-Dimethoxyphenyl)propanal 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 

Downstream Products

• 1448848-26-7 (R,E)-4-((tert-butyldimethylsilyl)oxy)-5-(3,4-dimethoxyphenyl)pent-2-en-1-ol 
• 1448848-32-5 C₁₉H₃₀O₄Si 
• 1448848-27-8 (R,2E,4E)-6-((tert-Butyldimethylsilyl)oxy)-7-(3,4-dimethoxyphenyl)-N-ethylhepta-2,4-dienamide 
• 1448848-33-6 C₂₃H₃₇NO₄Si 
• 1448848-28-9 (R,2E,4E)-ethyl 6-((tert-butyldimethylsilyl)oxy)-7-(3,4-dimethoxyphenyl)hepta-2,4-dienoate 
• 1448848-29-0 (R,2E,4E)-6-((tert-butyldimethylsilyl)oxy)-7-(3,4-dimethoxyphenyl)hepta-2,4-dienoic acid 
• 1448848-30-3 C₂₅H₂₇F₃O₇ 
• 1448848-25-6 (R,E)-ethyl-4-((tert-butyldimethylsilyl)oxy)-5-(3,4-dimethoxyphenyl)pent-2-enoate 
• 1448848-31-4 C₂₅H₂₇F₃O₇ 

Relevant academic research and scientific papers

First stereoselective synthesis of cytotoxic (-)-kunstleramide

The first stereoselective synthesis of the cytotoxic (-)-kunstleramide (1) has been reported from simple and commercially available starting material 3,4-dimethoxyphenylpropanol. The key steps involved are the MacMillan α-hydroxylation, Horner-Wadsworth-E