956024-19-4

Upstream product

• 956024-13-8 4,7-di(p-(t-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxole-5,6-dione 
• 21505-20-4 1,2-dihydroxy-4,5-methylenedioxybenzene 
• 956024-12-7 5,6-bis(methoxymethoxy)-4,7-di(p-(t-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxole 
• 956024-11-6 5,6-bis(methoxymethoxy)benzo[1,3]dioxole-4,7-diyl bis(trifluoromethanesulfonate) 
• 956024-10-5 5,6-bis(methoxymethoxy)benzo[d][1,3]dioxole-4,7-diol 
• 956024-09-2 5,6-bis(methoxymethoxy)benzo[d][1,3]dioxole 

Downstream Products

• 956024-14-9 5,6-bis(phenylacetoxy)-4,7-di(p-(t-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxole 
• 858134-23-3 4,5',6',4''-tetrahydroxy-2',3'-di(phenylacetoxy)-[1,1';4',1''-terphenyl] 
• 956024-15-0 5,6-bis(phenylacetoxy)-4,7-di(p-(t-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate 
• 1160726-23-7 5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxole 

Relevant academic research and scientific papers

Structural revision of thelephantin G by total synthesis and the inhibitory activity against TNF-α production

(Chemical Equation Presented) This paper describes the total synthesis of thelephantin G, thus revising the proposed structure 1 to 2. The key steps involved a double Suzuki-Miyaura coupling and an esteri-fication reaction. By a similar strategy, ganbajun

First total synthesis of vialinin A, a novel and extremely potent inhibitor of TNF-α production

Vialinin A, a powerful inhibitor (IC50 90 pM) of TNF-α production, was synthesized from sesamol in 11 steps with 28% overall yield. The key reactions include a double Suzuki coupling of electron-rich aryl triflate with phenylboronic acid and an