1261079-22-4

Upstream product

• 1261079-21-3 1,3,4-tris(4-methoxyphenyl)-1H-pyrrole 
• 68-12-2 N,N-dimethyl-formamide 
• 5703-26-4 4-Methoxyphenylacetaldehyde 
• 104-94-9 4-methoxy-aniline 
• 768-60-5 4-methoxyphenylacetylen 
• 106-37-6 1.4-dibromobenzene 
• 1453503-98-4 4-(2-{[(1,1-dimethylethyl)dimethyl]silyl}ethynyl)anisole 
• 16116-78-2 (4-bromophenyl)(trimethylsilyl)acetylene 

Downstream Products

• 1129697-15-9 2-methoxycarbonyl-3,4-di(4-methoxyphenyl)-N-4-methoxyphenylpyrrole 
• 1261079-21-3 1,3,4-tris(4-methoxyphenyl)-1H-pyrrole 
• 1261079-23-5 C₂₆H₂₃NO₅ 

Relevant academic research and scientific papers

Trimethylsilyl-Protected Alkynes as Selective Cross-Coupling Partners in Titanium-Catalyzed [2+2+1] Pyrrole Synthesis

Trimethylsilyl (TMS)-protected alkynes served as selective alkyne cross-coupling partners in titanium-catalyzed [2+2+1] pyrrole synthesis. Reactions of TMS-protected alkynes with internal alkynes and azobenzene under the catalysis of titanium imido comple

Total synthesis of lamellarins D, H, and R and ningalin B

A concise total synthesis of lamellarins D (7 steps), H (7 steps), and R (5 steps) and ningalin B (5 steps) is achieved starting from the corresponding aldehydes and amines. The synthesis features three oxidative reactions as key steps in a biomimetic manner, involving an AgOAc-mediated oxidative coupling reaction to construct the pyrrole core, a Pb(OAc)4-induced oxidative cyclization to form the lactone, and Kita's oxidation reaction to form the pyrrole-arene C-C bond.