A short and efficient synthesis of the substituted tetramines 2a and 7
and of the gadolinium complex 1 was developed starting from the Cbz-p
rotected amino alcohol 3. Key steps of the synthesis are the optimized
bleach oxidation of enantiopure alcohols and the bridging of the resu
lting aldehyde molecules by double reductive amination with ethylenedi
amine. Interesting biological activity of the amines 2a and 7 was dete
cted. (C) 1998 Elsevier Science Ltd. All rights reserved.