161869-02-9Relevant articles and documents
Lysine sulfonamides as novel HIV-protease inhibitors: Nε-Acyl aromatic α-amino acids
Stranix, Brent R.,Lavallee, Jean-Francois,Sevigny, Guy,Yelle, Jocelyn,Perron, Valerie,LeBerre, Nicholas,Herbart, Dominik,Wu, Jinzi J.
, p. 3459 - 3462 (2006)
A series of lysine sulfonamide analogues bearing Nε-acyl aromatic amino acids were synthesized using an efficient synthetic route. Evaluation of these novel protease inhibitors revealed compounds with high potency against wild-type and multiple-protease inhibitor-resistant HIV viruses.
Pictet-Spengler cyclization of 3,3-diphenylalanine (DIP) (III), synthesis of optically pure 1,2,3,4-tetrahydro-4-phenyl-3-isoquinolinecarboxylic acids, novel α-amino acids for peptides of biological interest
Chen,Goel
, p. 49 - 56 (1995)
All four isomers of 1,2,3,4-tetrahydro-4-phenyl-3-isoquinolinecarboxylic acid have been synthesized in high optical purity for the synthesis of peptides of biological interest.