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Synthesis and properties of arylheteroaliphatic aminoamides

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Abstract

The preparative synthesis of bioactive arylheteroaliphatic N-substitued aminoamides based on the opening of epoxide ring of styrene oxide followed by acylation of diaminoalcohols with acyl chlorides, was developed.

About the Authors

A. Kh. Mohammed
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


N. Yu. Borisova
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


E. Ya. Borisova
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


References

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3. Kitchen L.J., Polard C.B. Monoalkylalklation of ethylenediamine with alkene oxide // J. Org. Chem. 1943. V. 8 (4). P. 342-343.

4. Мохаммед А.Х., Борисова Е.Я., Егорова В.В., Крылов А.В., Борисова Н.Ю. Региоселективность раскрытия эпоксидного цикла окиси стирола этилендиаминами в различных средах // Вестник МИТХТ. 2011. Т. 6. № 5. С. 140-142.


Review

For citations:


Mohammed A.K., Borisova N.Yu., Borisova E.Y. Synthesis and properties of arylheteroaliphatic aminoamides. Fine Chemical Technologies. 2011;6(6):69-71. (In Russ.)

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ISSN 2410-6593 (Print)
ISSN 2686-7575 (Online)