202067-20-7

Upstream product

• 202067-11-6 (4R,5R)-4,5-isopropylidenedioxy-14-en-pentadecanol 
• 59101-26-7 pentadeca-4t,14-dien-1-ol 
• 202067-12-7 (4R,5R)-Pentadec-14-ene-1,4,5-triol 
• 720678-33-1 (4R,5R)-5-hydroxypentadec-14-en-1,4-olide 

Downstream Products

• 202067-15-0 Benzoic acid 2-benzenesulfonyl-4-((4R,5R)-5-dec-9-enyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-[2-((4R,5R)-5-decyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl]-butyl ester 
• 202067-13-8 (4R,5R)-4-(3-Benzenesulfonyl-propyl)-5-dec-9-enyl-2,2-dimethyl-[1,3]dioxolane 
• 720678-54-6 3-(4-Benzoyl-phenyl)-propionic acid (R)-11-{(2R,5R,2'R,5'R)-5'-[(1R,12R)-12-(tert-butyl-dimethyl-silanyloxy)-1-methoxymethoxy-13-((S)-5-methyl-2-oxo-2,5-dihydro-furan-3-yl)-tridecyl]-octahydro-[2,2']bifuranyl-5-yl}-11-methoxymethoxy-undecyl ester 
• 720678-52-4 4-tert-butyldimethylsilyloxy-15,24-di(methoxymethoxy)-34-(p-methoxybenzyloxymethyloxy)asimicin 
• 720678-51-3 {(E,Z)}-4-tert-butyldimethylsilyloxy-15,24-di(methoxymethoxy)-34-(p-methoxybenzyloxy)methyloxyasimicin-9-en-11-yne 
• 720678-41-1 (4R,5R,8R,9R,12R,13R)-1-tert-butyldimethylsilyloxy-4,13-di(methoxymethoxy)-23-(p-methoxybenzyloxy)methoxy-5,8,9,12-dioxidotricosane 
• 720678-44-4 (5R,6R,9R,10R,13R,14R)-1,1-dibromo-5,14-di(methoxymethoxy)-24-(p-methoxybenzyloxy)methoxy-6,9,10,13-dioxidotricos-1-ene 
• 720678-26-2 (5R,6R,9R,10R,13R,14R)-5,14-di(methoxymethoxy)-24-(p-methoxybenzyloxy)methoxy-6,9,10,13-dioxidotricos-1-yne 
• 720678-42-2 (4R,5R,8R,9R,12R,13R)-4,13-di(methoxymethoxy)-23-(p-methoxybenzyloxy)methoxy-5,8,9,12-dioxidotricosan-1-ol 
• 720678-34-2 (cis,4R,5R,12R,13R)-5-tert-butyldiphenylsilyloxytricos-12,13-isopropylidenedioxy-8,22-dien-1,4-olide 
• 720678-57-9 (R)-4-{(2R,5R,2'R,5'R)-5'-[(R)-11-(4-Methoxy-benzyloxymethoxy)-1-methoxymethoxy-undecyl]-octahydro-[2,2']bifuranyl-5-yl}-4-methoxymethoxy-butyraldehyde 

Relevant academic research and scientific papers

A convergent synthesis of (+)-parviflorin, (+)-squamocin K, and (+)-5S- hydroxyparviflorin

Thirty of the thirty-five carbon atoms of the acetogenin (+)-parviflorin (3, also named squamocin E) in this highly convergent synthesis derive from the building block, the readily accessible alcohol 1. The remaining five have their origin in an alkyne ob

Total Synthesis of 34-Hydroxyasimicin and Its Photoactive Derivative for Affinity Labeling of the Mitochondrial Complex I

The asymmetric total synthesis of the 34-hydroxyasimicin and its 3-(4-benzoylphenyl)propionate ester was achieved by means of a convergent synthetic strategy. This ester, which contains eight asymmetric centers, represents the first photoaffinity-labeling