600737-85-7

Upstream product

• 70-78-0 3-Iodo-L-tyrosine 
• 501-53-1 benzyl chloroformate 
• 79677-62-6 (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid 
• 213757-66-5 (S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid benzyl ester 
• 100-39-0 benzyl bromide 
• 5513-40-6 benzyl N-carbobenzyloxy-L-tyrosine 
• 315203-50-0 N-benzyloxycarbonyl-O-benzyl-L-tyrosine benzyl ester 
• 600737-79-9 benzyl (S)-3-(4-(benzyloxy)-3-iodophenyl)-2-(((benzyloxy)carbonyl)amino)propanoate 
• 600737-82-4 (S)-2-Benzyloxycarbonylamino-3-[4-benzyloxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine

An efficient synthesis of dityrosine and the first syntheses of the tyrosine trimers trityrosine and pulcherosine have been achieved. Protected 3-iodotyrosine underwent tandem Miyaura borylation-Suzuki coupling to give protected dityrosine. The choice of

A convenient preparation of dityrosine via Miyaura borylation-Suzuki coupling of iodotyrosine derivatives

Dityrosine has been prepared from 3-iodo-L-tyrosine derivatives by sequential Miyaura borylation and Suzuki coupling reactions. A tandem borylation-coupling protocol results in improved yields of the dityrosine derivatives. Suitable protecting group strat