Synthesis of new daunorubicin N-derivatives by one-step reductive amination


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Abstract

One-step reductive amination of aromatic aldehydes using an anthracycline antibiotic daunorubicin resulted in the preparation of its new N-derivatives, which are of interest as potential antitumor drugs.

About the authors

O. I. Artyushin

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

E. V. Sharova

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

N. M. Vinogradova

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

G. K. Genkina

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

A. A. Moiseeva

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

A. A. Khodak

Nesmeyanov Institute of Organoelemental Compounds

Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991

V. K. Brel

Nesmeyanov Institute of Organoelemental Compounds

Author for correspondence.
Email: v_brel@mail.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991


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