Transesterification of Exocyclic Ester Group of Methyl Pheophorbide a
- Autores: Tulaeva L.1, Gileva N.1, Belykh D.2
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Afiliações:
- P. Sorokin Syktyvkar State University
- Institute of Chemistry, Federal Research Center
- Edição: Volume 89, Nº 9 (2019)
- Páginas: 1772-1776
- Seção: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223066
- DOI: https://doi.org/10.1134/S107036321909007X
- ID: 223066
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Resumo
The reaction of methyl pheophorbide a with various alcohols in toluene in the presence of dimethylaminopyridine as a base was investigated. Under these conditions, a chemoselective transesterification of the exocyclic ring proceeds without the use of an activating agent (N-methyl-2-chloropyridinium iodide) or a catalyst (molecular iodine).
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Sobre autores
L. Tulaeva
P. Sorokin Syktyvkar State University
Autor responsável pela correspondência
Email: tulaeva65@mail.ru
Rússia, Oktyabrskii pr. 55, Syktyvkar, 167001
N. Gileva
P. Sorokin Syktyvkar State University
Email: tulaeva65@mail.ru
Rússia, Oktyabrskii pr. 55, Syktyvkar, 167001
D. Belykh
Institute of Chemistry, Federal Research Center
Email: tulaeva65@mail.ru
Rússia, Syktyvkar
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