Convenient preparation of optically active N,N-bis(4-substituted-4-aminobutyl)amines

Add time:08/10/2019    Source:sciencedirect.com

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 activities.

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