925230-87-1

Upstream product

• 924708-53-2 (S)-2-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)propan-1-ol 
• 6336-44-3 (E)-propenylboronic acid 
• 159191-56-7 (4-((tert-butyldimethylsilyl)oxy)phenyl)boronic acid 
• 924708-50-9 (R)-1-(2-(4-(tert-butyldimethylsilyloxy)phenoxy)-5-iodophenyl)ethane-1,2-diol 
• 924708-51-0 (R)-tert-butyl(4-(4-iodo-2-(oxiran-2-yl)phenoxy)phenoxy)dimethylsilane 
• 1761-62-2 5-iodosalicyclaldehyde 
• 924708-52-1 toluene-4-sulfonic acid 2-{2-[4-(tert-butyl-dimethyl-silanyloxy)-phenoxy]-5-iodo-phenyl}-2-hydroxy-ethyl ester 
• 924708-49-6 tert-butyl(4-(4-iodo-2-vinylphenoxy)phenoxy)dimethylsilane 
• 924708-48-5 4-iodo-2-ethenylphenol 

Relevant academic research and scientific papers

Total synthesis of rodgersinol: A survey of the Cu(II)-mediated coupling of ortho-substituted phenols

Full details of studies directed toward the total synthesis of both enantiomers of rodgersinol are described. The key parts of our synthetic route to rodgersinol included the Cu(II)-mediated coupling of an arylboronic acid with an ortho-alkyl substituted

Concise synthesis of rodgersinol and determination of the C-10 absolute configuration

Rodgersinol was synthesized via seven linear steps in 31% overall yield, and the absolute configuration of the C-10 stereogenic center was elucidated. The key feature of the synthesis involves the efficient Cu(II)-mediated coupling of two aromatic moietie