52186-44-4Relevant academic research and scientific papers
A new approach to the synthesis of l-3-hydroxy-4-methoxy-5-methyl-phenylalanine derivatives from l-tyrosine
Chen, Ruijiao,Zhu, Deguang,Hu, Zuoqiang,Zheng, Zhiming,Chen, Xiaochuan
experimental part, p. 39 - 42 (2010/04/24)
A practical procedure to regioselectively install a methyl group and a phenolic hydroxyl group onto l-tyrosine was developed. By using this approach, protected l-3-hydroxy-4-methoxy-5-methyl-phenylalanine and l-3-hydroxy-4-methoxy-5-methyl-phenylalanol, which are utilized in efficient syntheses of the relevant tetrahydroisoquinoline alkaloids, were prepared conveniently with high yield.
Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine - Phenol dimers
Bew, Sean P.,Hughes, David L.,Sharma, Sunil V.
, p. 7881 - 7884 (2007/10/03)
(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
A convenient two step transformation of tyrosine into the antihypertensive amino acid (S)-4-hydroxy-3-hydroxymethylphenylalanine
Allevi, Pietro,Cribiu, Riccardo,Anastasia, Mario
, p. 1355 - 1358 (2007/10/03)
Treatment of tyrosine with paraformaldehyde and catalytic amounts of p-toluenesulfonic acid, at reflux in toluene, directly generates benzyl (S)-4-(4H-1,3-benzodioxin-6-ylmethyl)-5-oxo-1,3-oxazolane-3-carboxylate, which on treatment with boron trichloride in dichloromethane, affords (S)-4-hydroxy-3-hydroxymethylphenylalanine.
An Alternative Synthesis of the Enantiomerically Pure Competitive NMDA Antagonists SDZ 220-581 and SDZ EAB 515
Müller, Werner,B?nziger, Markus,Kipfer, Peter
, p. 729 - 733 (2007/10/03)
An alternative synthesis of enantiomerically pure SDZ 220-881 (1a) and SDZ EAB 515 (1b) starting from L-Z-tyrosine is described.
