292820-08-7

Upstream product

• 292820-17-8 (2S,5R)-2-Hydroxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran 
• 292820-05-4 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid 
• 292820-15-6 1-(1',4'-Dihydroxybutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 
• 80810-40-8 1-(4'-Oxobutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 
• 80810-55-5 1-(4'-Hydroxybutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 
• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 292820-16-7 (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran 
• 292820-07-6 (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran 

Downstream Products

• 292820-09-8 Hydroquinone-mucocin dimethyl ether 
• 337954-04-8 19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether 

Relevant academic research and scientific papers

Quinone - Annonaceous acetogenins: Synthesis and complex I inhibition studies of a new class of natural product hybrids

The natural product hybrids quinone-mucocin and quinone- squamocin D were synthesized. In these hybrids, the butenolide unit of the annonaceous acetogenins mucocin and squamocin D is exchanged for the quinone moiety of the natural complex I substrate ubiq

Natural-product hybrids: Design, synthesis, and biological evaluation of quinone - Annonaceous acetogenins

Replacement of the butyrolactone unit of the natural products with a quinone subunit has resulted in the synthesis of natural-product hybrids of quinone-mucocin (1). These compounds, which are combined from partial structures of annonaceous acetogenins an