842166-51-2Relevant academic research and scientific papers
Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131
Tamamura, Hirokazu,Hiramatsu, Kenichi,Ueda, Satoshi,Wang, Zixuan,Kusano, Shuichi,Terakubo, Shigemi,Trent, John O.,Peiper, Stephen C.,Yamamoto, Naoki,Nakashima, Hideki,Otaka, Akira,Fujii, Nobutaka
, p. 380 - 391 (2007/10/03)
L,L-Type and L,D-type (E)-alkene dipeptide isosteres (EADIs) that have unnatural side chains at the α-position were synthesized by the combination of stereoselective aziridinyl ring-opening reactions and organozinc-copper-mediated anti-SN2′ rea
