405519-75-7

Upstream product

• 405519-74-6 C₂₁H₂₇BrO₃Si 
• 405519-73-5 7-bromo-3-(tert-butyl-dimethyl-silanyloxymethyl)-3-phenyl-3H-benzofuran-2-one 
• 405519-72-4 7-bromo-3-hydroxymethyl-3-phenyl-3H-benzofuran-2-one 
• 611-71-2 MANDELIC ACID 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 95-56-7 2-hydroxybromobenzene 
• 195873-89-3 7-Bromo-3-phenyl-3H-benzofuran-2-one 

Downstream Products

• 405519-79-1 4-[3-(tert-butyl-dimethyl-silanyloxymethyl)-3-phenyl-2,3-dihydro-benzofuran-7-yl]-3-[2-(tert-butyl-diphenyl-silanyloxymethyl)-oxazol-5-yl]-1-methoxymethyl-1H-indole 
• 405519-88-2 C₃₁H₂₁Cl₂N₃O₄ 
• 405519-84-8 C₃₁H₂₅N₃O₅ 
• 405519-83-7 C₃₁H₂₇N₃O₅ 
• 405519-86-0 C₃₀H₂₁N₃O₄ 
• 405519-85-9 C₃₁H₂₃N₃O₄ 
• 405519-80-4 {7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-3-phenyl-2,3-dihydro-benzofuran-3-yl}-methanol 
• 405519-81-5 5-[4-(3-formyl-3-phenyl-2,3-dihydro-benzofuran-7-yl)-1-methoxymethyl-1H-indol-3-yl]-oxazole-2-carbaldehyde 

Relevant academic research and scientific papers

SYNTHESIS OF DIAZONAMIDE "A" CORE

Using a novel samarium (II)-based macrocyclization cascade reaction, the entire highly strained ABCDEF aromatic core of diazonamide "A" and several novel analogies thereof are constructed.

Construction of the complete aromatic core of diazonamide A by a novel hetero pinacol macrocyclization cascade reaction

One of the most enticing natural products isolated in recent years and a serious challenge to synthetic chemists is represented by the potent anticancer agent diazonamide A (1). By utilizing a highly convergent approach, the ABCDEF macrocycle 2 was constr