212010-24-7Relevant articles and documents
A highly efficient asymmetric synthesis of methoxyhomophenylalanine using Michael addition of phenethylamine
Yamada, Masahiko,Nagashima, Nobuo,Hasegawa, Junzo,Takahashi, Satomi
, p. 9019 - 9022 (1998)
A practical method for (S)-p-methoxyhomophenylalanine (S)-1 by using diastereoselective Michael addition as a key step was reported. Thus, the Michael addition of (S)-1-phenethylamine (S)-3 to p-methoxy-trans- benzoylacrylic acid 2 was performed in a high
Stereoselective syntheses of fluorescent non-natural aromatic amino acids based on asymmetric michael additions
Chen, Heru,Zhong, Xianbin,Wei, Jin
, p. 1170 - 1182 (2008/02/05)
Four fluorescent non-natural aromatic amino acids have been synthesized based on a key stereoselective Michael addition reaction. S-1-Phenylethylamine was employed as both the source of amine and the stereoselectivity controller. The overall yields were m