875654-41-4

Upstream product

• 7368-78-7 4-bromoguaiacol 
• 271243-19-7 2-isopropoxy-1-methoxy-4-((E)-2-nitrovinyl)benzene 
• 271243-18-6 2-(3-Isopropoxy-4-methoxyphenyl)-1-ethylamine 
• 90-05-1 2-methoxy-phenol 
• 86636-00-2 3-isopropoxy-4-methoxyphenol 
• 138505-27-8 4-bromo-1-isopropoxy-2-methoxy-benzene 
• 34123-66-5 O-isopropylisovanillin 
• 875654-32-3 dimethyl 1-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-3,4-bis(trifluoromethanesulfonyloxy)pyrrole-2,5-dicarboxylate 
• 875654-36-7 dimethyl 3,4-dihydroxy-1-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]pyrrole-2,5-dicarboxylate 
• 875654-35-6 dimethyl N-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]iminodiacetate 
• 875654-38-9 1-bromo-4-isopropoxy-5-methoxy-2-methoxymethoxybenzene 
• 875654-33-4 4-isopropoxy-3-methoxyphenylboronic acid 
• 875654-37-8 2-isopropoxy-1-methoxy-4-methoxymethoxybenzene 
• 875654-34-5 4-isopropoxy-5-methoxy-2-methoxymethoxyphenylboronic acid 

Downstream Products

• 875654-43-6 3,4-dihydro-7-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrole-2-carboxylic acid 
• 97614-65-8 lamellarin D 
• 660396-69-0 5,6-dihydro-3,11-diisopropoxy-14-(4-isopropoxy-3-methoxyphenyl)-2,12-dimethoxy-6H-[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one 
• 660396-67-8 3,11-diisopropoxy-14-(4-isopropoxy-3-methoxyphenyl)-2,12-dimethoxy-6H-chromeno[4′,3′:4,5]pyrrolo[2,1-a]-isoquinolin-6-one 
• 875654-30-1 7-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrol-4(3H)-one 

Relevant academic research and scientific papers

Total synthesis of lamellarins D, L, and N

Total synthesis of cytotoxic marine alkaloids, lamellarins D, L, and N, has been achieved by using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki-Miyaura coupling of the 3,4-dihydroxypyrrole bistriflate 6 as the key reactions. The total yields of lamellarins D, L, and N from the common intermediate 6 are 54, 58, and 50%, respectively.