Phosphorylation of emodin

descriptionPublicationkeyboard_double_arrow_right Article 01 Mar 1994 English Publisher:Springer Science and Business Media LLCJournal:Chemistry of Natural Compounds, volume 30, pages 193-196 (issn: 0009-3130, eissn: 1573-8388,

Copyright policy )

Authors: L. N. Pribytkova; M. S. Erzhanova;

doi: 10.1007/bf00630003

Phosphorylation of emodin

- Summary
- Metrics

Abstract

A convenient method has been developed for the interaction of dialkyl phosphites with 1,6,8-trihydroxy-3-methylanthraquinone (emodin) under the conditions of the Todd—Atherton reaction. It has been shown that the α-hydroxy groups of emodin are not phosphorylated at an equimolar ratio of emodin and dialkyl phosphite. The phosphorylation of 7-bromo-1,6,8-trihydroxy-3-methylanthraquinone with potassium dialkyl phosphorothioates has been studied. The reaction takes place at the sulfur atom, with the formation of of the product of S-alkylation.

Impact byBIP!

	selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	1
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Average
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average