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Synthesis, structure and antiproliferative activity of chiral polyamines based on a 2-azanorbornane skeleton.
Autorzy
Rok wydania
2016
Czasopismo
Numer woluminu
27
Strony
753-758
DOI
10.1016/j.tetasy.2016.06.009
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
A series of enantiopure 2-azanorbornane-based amines were prepared via a stereoselective aza-Diels–Alder reaction and further modifications of the obtained cycloadduct. In particular, derivatives containing two bicyclic moieties linked by N—C—C—N fragments were synthesized. Two dimeric derivatives exhibited a significant antiproliferative activity against selected cell lines, comparable to cisplatin in certain cases.
Adres publiczny
http://dx.doi.org/10.1016/j.tetasy.2016.06.009
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