Transesterification of Exocyclic Ester Group of Methyl Pheophorbide a
- Авторы: Tulaeva L.1, Gileva N.1, Belykh D.2
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Учреждения:
- P. Sorokin Syktyvkar State University
- Institute of Chemistry, Federal Research Center
- Выпуск: Том 89, № 9 (2019)
- Страницы: 1772-1776
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223066
- DOI: https://doi.org/10.1134/S107036321909007X
- ID: 223066
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Аннотация
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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Об авторах
L. Tulaeva
P. Sorokin Syktyvkar State University
Автор, ответственный за переписку.
Email: tulaeva65@mail.ru
Россия, Oktyabrskii pr. 55, Syktyvkar, 167001
N. Gileva
P. Sorokin Syktyvkar State University
Email: tulaeva65@mail.ru
Россия, Oktyabrskii pr. 55, Syktyvkar, 167001
D. Belykh
Institute of Chemistry, Federal Research Center
Email: tulaeva65@mail.ru
Россия, Syktyvkar