Transesterification of Exocyclic Ester Group of Methyl Pheophorbide a
- 作者: Tulaeva L.1, Gileva N.1, Belykh D.2
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隶属关系:
- P. Sorokin Syktyvkar State University
- Institute of Chemistry, Federal Research Center
- 期: 卷 89, 编号 9 (2019)
- 页面: 1772-1776
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223066
- DOI: https://doi.org/10.1134/S107036321909007X
- ID: 223066
如何引用文章
详细
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).
作者简介
L. Tulaeva
P. Sorokin Syktyvkar State University
编辑信件的主要联系方式.
Email: tulaeva65@mail.ru
俄罗斯联邦, Oktyabrskii pr. 55, Syktyvkar, 167001
N. Gileva
P. Sorokin Syktyvkar State University
Email: tulaeva65@mail.ru
俄罗斯联邦, Oktyabrskii pr. 55, Syktyvkar, 167001
D. Belykh
Institute of Chemistry, Federal Research Center
Email: tulaeva65@mail.ru
俄罗斯联邦, Syktyvkar