Synthesis of azamacrocyclic compounds by cyclocondensation of aliphatic α,ω-diamines with acetone
- Autores: Anisimova N.1, Khristoforova E.1, Trishin Y.1
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Afiliações:
- St. Petersburg State University of Industrial Technology and Design
- Edição: Volume 86, Nº 9 (2016)
- Páginas: 2047-2051
- Seção: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/216129
- DOI: https://doi.org/10.1134/S1070363216090115
- ID: 216129
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Resumo
Cyclocondensation of 1,4-diaminobutane and 1,6-diaminohexane with acetone afforded the corresponding 18- and 22-membered trans-azamacrocyclic Curtis compounds in high yield, which contain two azomethine and amine nitrogen atoms. A complex mixture of the products formed containing less than 25% of 16-membered azamacrocyclic cis- and trans-isomers when reacting 1,3-diaminopropane with acetone.
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Sobre autores
N. Anisimova
St. Petersburg State University of Industrial Technology and Design
Email: trish@YT4470.spb.edu
Rússia, ul. I. Chernykh 4, St. Petersburg, 198095
E. Khristoforova
St. Petersburg State University of Industrial Technology and Design
Email: trish@YT4470.spb.edu
Rússia, ul. I. Chernykh 4, St. Petersburg, 198095
Yu. Trishin
St. Petersburg State University of Industrial Technology and Design
Autor responsável pela correspondência
Email: trish@YT4470.spb.edu
Rússia, ul. I. Chernykh 4, St. Petersburg, 198095
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