212010-24-7Relevant academic research and scientific papers
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
A novel β-amino acid in cytotoxic peptides from the cyanobacterium Tychonema sp.
Mehner, Christian,Mueller, Daniela,Krick, Anja,Kehraus, Stefan,Loeser, Reik,Guetschow, Michael,Maier, Armin,Fiebig, Heinz-Herbert,Brun, Reto,Koenig, Gabriele M.
supporting information; experimental part, p. 1732 - 1739 (2009/04/07)
The cyclic dodecapeptides tychonamide A (1) and B (2) isolated from the methanolic extract of the cyanobacterium Tychonema sp. contain the novel β-amino acid 3-amino-2,5,7-trihydroxy-8-phenyloctanoic acid (Atpoa). Compounds 1 and 2 have cytotoxic activity
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
