327163-78-0

Upstream product

• 85432-87-7 2-bromo-3,6-dimethoxybenzaldehyde 
• 420-37-1 trimethoxonium tetrafluoroborate 
• 241127-72-0 2-bromo-3,6-dihydroxy-benzaldehyde 
• 327163-76-8 methyl 3,6-dimethoxy-2-nitrobenzoate 
• 208986-13-4 methyl 2-amino-3,6-dimethoxybenzoate 
• 327164-05-6 (2-bromo-3,6-dimethoxyphenyl)methanol 
• 327163-77-9 methyl 2-bromo-3,6-dimethoxybenzoate 

Downstream Products

• 327163-79-1 2-bromo-3-methoxy-6-(2-propenyloxy)benzaldehyde 
• 917113-25-8 C₈H₉BrO₃ 
• 327163-81-5 2-bromo-3,6-dimethoxy-5-(2-propenyl)benzaldehyde 
• 327163-80-4 2-bromo-6-hydroxy-3-methoxy-5-(2-propenyl)benzaldehyde 
• 327163-82-6 1-bromo-2-(dimethoxymethyl)-3,6-dimethoxy-4-(2-propenyl)benzene 
• 327163-84-8 [2-(dimethoxymethyl)-3,6-dimethoxy-4-(2-propenyl)phenyl]methanol 
• 327163-83-7 methyl 3,6-dimethoxy-2-(dimethoxymethyl)-4-(2-propenyl)benzoate 
• 1332271-49-4 C₅₇H₉₂BrClO₁₂Si₄ 
• 1332271-50-7 C₅₀H₈₆BrClO₁₂Si₄ 
• 1332271-55-2 C₈H₉BrO₂ 
• 1332271-10-9 C₉H₉BrO₃ 
• 1332271-56-3 C₁₇H₁₇BrO₄ 
• 1332271-57-4 C₁₈H₁₉BrO₃ 
• 1332271-11-0 C₁₈H₂₁BrO₅ 

Relevant academic research and scientific papers

Sporolide B: Synthetic studies

Studies directed toward the synthesis of the architecturally complex marine natural product sporolide B are described. Synthetic analysis suggested advanced hydroquinone and benzodiquinane fragments, which upon elaboration were successfully united via an

Total synthesis of the diazobenzofluorene antibiotic (-)-kinamycin C 1

The enantioselective total synthesis of the diazobenzofluorene antibiotic (-)-kinamycin C is reported. The approach involves tartrate-mediated, asymmetric nucleophilic epoxidation of a functionalized quinone monoketal to construct the highly substituted D

Synthesis of (+/-)-puraquinonic acid: an inducer of cell differentiation.

Puraquinonic acid (1) was synthesized from 2,5-dimethoxybenzoic acid by way of isochroman 2 and the indanone derivative 3, a Nazarov cyclization being used to construct the five-membered ring.