206445-91-2

Upstream product

• 52186-44-4 (S)-N-benzyloxycarbonyl-4-hydroxy-3-hydroxymethylphenylalanine 
• 1164-16-5 Z-L-Tyr-OH 
• 67-56-1 methanol 

Downstream Products

• 206445-92-3 (S)-2-Benzyloxycarbonylamino-3-(8-bromo-2,2-dimethyl-4H-benzo[1,3]dioxin-6-yl)-propionic acid methyl ester 
• 206445-95-6 (S)-3-(5-Acetoxymethyl-2'-chloro-6-trifluoromethanesulfonyloxy-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-96-7 (S)-3-(5-Acetoxymethyl-6-trifluoromethanesulfonyloxy-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-93-4 (S)-3-(5-Acetoxymethyl-2'-chloro-6-hydroxy-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-97-8 (S)-3-(5-Acetoxymethyl-2'-chloro-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-94-5 (S)-3-(5-Acetoxymethyl-6-hydroxy-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-98-9 (S)-3-(5-Acetoxymethyl-biphenyl-3-yl)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 206445-99-0 (S)-2-Benzyloxycarbonylamino-3-(5-bromomethyl-2'-chloro-biphenyl-3-yl)-propionic acid methyl ester 
• 206446-00-6 (S)-2-Benzyloxycarbonylamino-3-(5-bromomethyl-biphenyl-3-yl)-propionic acid methyl ester 

Relevant academic research and scientific papers

An Alternative Synthesis of the Enantiomerically Pure Competitive NMDA Antagonists SDZ 220-581 and SDZ EAB 515

An alternative synthesis of enantiomerically pure SDZ 220-881 (1a) and SDZ EAB 515 (1b) starting from L-Z-tyrosine is described.

Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine - Phenol dimers

(Chemical Equation Presented) The efficient synthesis of 2,2′-arylmethylene dimers from 3-hydroxymethyl or 3-methoxymethyl-5-halo- (S)-tyrosines and para-substituted phenols under acid-catalyzed reaction conditions using either conventional or microwave-a