339221-02-2

Upstream product

• 339220-96-1 (2S,3R)-2-[3-(4-Benzyloxy-phenyl)-propyl]-3-[(S)-2-(4-hydroxy-3-iodo-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-5-methyl-hexanoic acid tert-butyl ester 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 70277-02-0 3-iodo-L-tyrosine methyl ester 
• 339220-93-8 (2S,3R)-2-[3-(4-Benzyloxy-phenyl)-propyl]-3-isobutyl-succinic acid 1-tert-butyl ester 
• 191407-39-3 1-(benzyloxy)-4-(3-iodopropyl)benzene 
• 112245-04-2 (R)-2-(2-(tert-butoxy)-2-oxoethyl)-4-methylpentanoic acid 

Downstream Products

• 339221-03-3 (2S,3R)-2-[3-(4-Benzyloxy-phenyl)-propyl]-3-{(S)-1-methoxycarbonyl-2-[4-methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-ethylcarbamoyl}-5-methyl-hexanoic acid tert-butyl ester 
• 339221-00-0 (2S,3R)-2-[3-(4-Hydroxy-phenyl)-propyl]-3-{(S)-1-methoxycarbonyl-2-[4-methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-ethylcarbamoyl}-5-methyl-hexanoic acid tert-butyl ester 
• 339221-08-8 C₃₂H₄₆BNO₉ 

Relevant academic research and scientific papers

Intramolecular O-arylation of phenols with phenylboronic acids: Application to the synthesis of macrocyclic metalloproteinase inhibitors

(matrix presented) The copper acetate mediated intramolecular O-arylation of phenols with phenylboronic acid pseudopeptides is the key step in the preparation of macrocyclic biphenyl ether hydroxamic acid inhibitors of collagenase 1 and gelatinases A and