202195-07-1

Upstream product

• 874-63-5 3,5-dimethylmethoxybenzene 
• 149402-07-3 3-allyl-2-bromo-1,4,5-trimethoxynaphthalene 
• 69008-03-3 2-bromo-5-hydroxy-[1,4]naphthoquinone 
• 110451-90-6 (2-bromo-5-methoxy-3-methylphenyl)methanol 
• 164513-49-9 2-bromo-1-(bromomethyl)-5-methoxy-3-methylbenzene 
• 119650-44-1 (3-methoxy-5-methylphenyl)methanol 
• 119650-45-2 (2-iodo-3-methoxy-5-methylphenyl)methanol 
• 199612-65-2 2-iodo-3-methoxy-5-methylbenzaldehyde 
• 69833-09-6 2-bromo-5-methoxy-[1,4]naphthoquinone 
• 869487-91-2 3-allyl-2-bromo-5-methoxynaphthalene-1,4-dione 
• 106116-42-1 1-bromomethyl-3-methoxy-5-methyl-benzene 
• 90674-26-3 3-methoxy-5-methyl-benzaldehyde 
• 107941-22-0 2-bromo-1,4,5-trimethoxynaphthalene 
• 202195-05-9 2-bromo-3-methoxy-5-methylbenzaldehyde 

Downstream Products

• 202195-03-7 3-Methoxy-5-methyl-2-(1',4',5'-trimethoxynaphthalen-2'-yl)benzoic acid 
• 85178-50-3 1-Hydroxy-8-methoxy-3-methylbenzanthracene-7,12-dione 
• 202195-14-0 Acetic acid 11-[(E)-benzyloxyimino]-4,5,9,10-tetramethoxy-11H-benzo[b]fluoren-2-ylmethyl ester 
• 202195-15-1 Acetic acid 11-[(E)-benzyloxyimino]-4,9-dimethoxy-5,10-dioxo-10,11-dihydro-5H-benzo[b]fluoren-2-ylmethyl ester 
• 202195-10-6 4,5,9,10-Tetramethoxy-2-methyl-benzo[b]fluoren-11-one O-benzyl-oxime 
• 202195-02-6 4,9-Dimethoxy-2-methyl-benzo[b]fluorene-5,10,11-trione 11-(O-benzyl-oxime) 

Relevant academic research and scientific papers

Reactions of [2-(2-Naphthyl)phenyl]acetylenes and 2-(2-Naphthyl)benzaldehyde O-Phenyloximes: Synthesis of the Angucycline Tetrangulol and 1,10,12-Trimethoxy-8-methylbenzo[c]phenanthridine

The Suzuki–Miyaura coupling reaction between (1,4,5-trimethoxynaphthalen-2-yl)boronic acid and 2-iodo-3-methoxy-5-methylbenzaldehyde gave the intermediate 3-methoxy-5-methyl-2-(1,4,5-trimethoxynaphthalen-2-yl)benzaldehyde. Conversion of this benzaldehyde

Total syntheses of O4,O9-dimethylstealthins A and C

O12-Acetyl-O4,O9-dimethylstealthin A (2-acetoxymethyl-11-amino-5-hydroxy-4,9-dimethoxybenzo[b]-fluoren-10-one and O4,O9-dimethylstealthin C (11-amino-5-hydroxy-4,9-dimethoxy-2-methylbenzo-[6]fluoren-10-one), methylated derivatives of potent radical scavengers produced by Streptomyces viridochromogenes, have been synthesized using Suzuki coupling as a key step.

Total syntheses of O4,9-dimethyl stealthins A and C

O4,9-dimethylstealthin A (11-amino-5-hydroxy-2-hydroxymethyl-4,9-dimethoxybenzo[b]fluoren-10-on e) and O4,9-dimethylstealthin C (11-amino-5-hydroxy-4,9-dimethoxy-2-methyl-benzo[b]fluoren-10-one), methylated derivatives of radical scavengers produced by Streptomyces viridochromogenes, were synthesized using the Suzuki coupling reactions as a key step.