620177-96-0

Upstream product

• 76280-60-9 [3,5-bis(methoxymethoxy)phenyl]methanol 
• 620177-94-8 methyl 2,6-dibromo-3,5-dihydroxybenzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 79834-15-4 (2-bromo-3,5-bis(methoxymethoxy)phenyl)methanol 

Downstream Products

• 620178-00-9 [3,5-dihydroxy-2-(3-methylbut-2-enyl)phenyl](3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone 
• 620177-97-1 [3,5-bis(methoxymethoxy)-2-(3-methylbut-2-enyl)phenyl][3,5-dichloro-2-methoxy-6-(methoxymethoxy)-4-methylphenyl]methanol 
• 620177-98-2 [3,5-bis(methoxymethoxy)-2-(3-methylbut-2-enyl)phenyl][3,5-dichloro-2-methoxy-6-(methoxymethoxy)-4-methylphenyl]methanone 
• 852612-20-5 1-{2,4-Bis-methoxymethoxy-6-[(E)-2-(4-methoxymethoxy-phenyl)-vinyl]-phenyl}-2-methyl-propan-1-one 
• 852612-19-2 2-Bromo-1,5-bis-methoxymethoxy-3-[(E)-2-(4-methoxymethoxy-phenyl)-vinyl]-benzene 
• 495412-14-1 3,5-bis(methoxymethoxy)-2-(3-methylbut-2-enyl)benzaldehyde 

Relevant academic research and scientific papers

Enantioselective total synthesis of aigialomycin D

An efficient, convergent approach for the total synthesis of aigialomycin D 1 is described. Key features of the synthetic strategy include (a) a Sharpless asymmetric epoxidation reaction and selective opening of a 2,3-epoxy alcohol to elaborate the two hy

First total synthesis of two resveratrol derivatives

The total synthesis of two resveratrol derivatives with an isobutyryl substituent is reported for the first time.

Synthetic analogues of the antibiotic pestalone

The first synthetic study towards the natural product pestalone (1) is described culminating in the preparation of selected n-1 analogues. Pestalone is a chlorinated and prenylated benzophenone antibiotic, which is of interest due to a strong activity aga