848983-56-2Relevant academic research and scientific papers
Convenient preparation of optically active N,N-bis(4-substituted-4- aminobutyl)amines
Tsubaki, Kazunori,Kusumoto, Tomokazu,Hayashi, Noriyuki,Tanima, Daisuke,Fuji, Kaoru,Kawabata, Takeo
, p. 739 - 743 (2007/10/03)
An efficient and convenient method for the synthesis of chiral triamines with two substituents at the α position to the terminal amino group (spermidine analogues) is described. These chiral N,N-bis(4-substituted-4- aminobutyl)amines may have anticancer a
