126383-89-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 143817-66-7 (S)-4-{3-[4-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-phenoxy]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 3978-80-1 Boc-Tyr-OH 
• 60-18-4 L-tyrosine 
• 126383-86-6 (S)-2-Amino-3-(3-bromo-4-methoxy-phenyl)-propan-1-ol 
• 20989-19-9 (2S)-2-amino-3-(4-methoxyphenyl)propan-1-ol 
• 126383-88-8 C₃₃H₃₄N₂O₆ 
• 126383-87-7 N-[(S)-2-(3-Bromo-4-methoxy-phenyl)-1-hydroxymethyl-ethyl]-benzamide 
• 10418-01-6 N-benzoyl-L-tyrosine methyl ester 
• 126455-12-7 (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)benzamide 
• 6230-11-1 O-Methyltyrosine 
• 143817-64-5 (R)-4-(3-{4-[(S)-2-tert-Butoxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenoxy}-4-methoxy-benzoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 143817-65-6 (R)-4-[(3-{4-[(S)-2-tert-Butoxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenoxy}-4-methoxy-phenyl)-hydroxy-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 143817-61-2 C₃₈H₄₈N₂O₉ 

Downstream Products

• 113311-30-1 (S)-2-Amino-3-{3-[4-((S)-2-amino-2-carboxy-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid 
• 113311-35-6 H-Isodityr-OMe 
• 126383-92-4 dihydrobromide of isodityrosine 
• 126383-90-2 (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of (S,S)-Isodityrosinol in a Fully Differentiated Form via Diels-Alder Methodology

A Diels-Alder cycloaddition reaction of an aryloxy diene 7 and an acetylenic ketone 8 derived, respectively, from L-tyrosine and D-serine leads to the synthesis of the diaryl ether unit common to isodityrosine, which upon elaboration provides the function

FACILE CHEMICAL SYTHESIS OF S,S-ISODITYROSINE, A NATURALLY-OCCURRING CROSS-LINKING AMINO ACID

Ullmann coupling of the two protected S-tyrosine derivatives 6 and 9 afforded the protected isodityrosine 10 which was converted into the natural bis-amino acid S,S-isodityrosine 1 in good yield.