199468-81-0Relevant articles and documents
Synthesis and conformational features of topographically constrained designer chimeric amino adds: The β-isopropyl phenylalanines
Liao, Subo,Shenderovich, Mark D.,Lin, Jun,Hruby, Victor J.
, p. 16645 - 16662 (2007/10/03)
All four optically pure isomers of the highly conformationally constrained novel chimeric amino acid, β-isopropylphenylalanine or β- phenylleucine, were asymmetrically synthesized in five to six steps in 20 - 25% overall yield. Computer-assisted molecular modeling revealed that the β- isopropyl group in these chimeric amino acids plays the dominant role in determining the most favorable side chain conformations.
Asymmetric synthesis of optically pure β-isopropylphenylalanine: A new β-branched unusual amino acid
Liao, Subo,Hruby, Victor J.
, p. 1563 - 1566 (2007/10/03)
All four optically pure isomers of a highly conformationally constrained unusual amino acid, β-isopropylphenylalanine, have been asymmetrically synthesized.