659746-80-2

Upstream product

• 659746-79-9 3-(methoxyiminomethyl)-2,4-bis(methoxymethyloxy)benzaldehyde 
• 13709-06-3 2,4-bis(methoxymethoxy)benzaldehyde 
• 659746-74-4 2,4-bis(methoxymethyloxy)benzyl alkohol 
• 659746-78-8 3-(methoxyiminomethyl)-2,4-bis(methoxymethyloxy)benzyl alcohol 
• 659746-75-5 1,3-bis(methoxymethyloxy)-4-(tert-butyldimethylsilyloxymethyl)benzene 
• 659746-76-6 2,6-bis(methoxymethyloxy-)-3-(tert-butyldimethylsilyloxymethyl)benzaldehyde 
• 659746-77-7 2-(methoxyiminomethyl)-1,3-bis(methoxymethyloxy)-4-(tert-butyldimethylsilyloxymethyl)benzene 

Downstream Products

• 659746-81-3 methyl [6-formyl-2-(methoxyiminomethyl)-3-(methoxymethyloxy)phenyloxy]acetate 
• 659746-82-4 methyl [6-formyl-3-hydroxy-2-(methoxyiminomethyl)phenyloxy]acetate 
• 659746-84-6 methyl [6-formyl-2-(methoxyiminomethyl)-3-(prop-1-en-1-yl)phenyloxy]acetate 
• 659746-83-5 methyl [6-formyl-2-(methoxyiminomethyl)-3-(trifluoromethanesulfonyloxy)phenyloxy]acetate 

Relevant academic research and scientific papers

Synthesis of the new furo[3,2-h]isoquinoline alkaloid, TMC-120B from Aspergillus ustus

A total synthesis of a new furo[3,2-h]isoquinoline alkaloid TMC120-B (2), isolated from Aspergillus ustus together with two related compounds, has been completed in sixteen steps. The key step is the synthesis of the appropriate 3,7,8-trisubstituted isoqu

A total synthesis of a new type of furo[3,2-h]isoquinoline alkaloid, TMC-120B

A total synthesis of a new furo[3,2-h]isoquinoline alkaloid, TMC-120B (2) has been completed in sixteen steps. The key step is the synthesis of 7,8-disubstituted isoquinoline (17) based on the thermal electrocyclic reaction of 1-azahexatriene system invol