Cyclodimerization of a citral dienamine

descriptionPublicationkeyboard_double_arrow_right Article 01 May 1991 English Publisher:Springer Science and Business Media LLCJournal:Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, volume 40, pages 1,067-1,070 (issn: 0568-5230, eissn: 1573-9171,

Copyright policy )

Authors: A. G. Nigmatov; �. P. Serebryakov;

doi: 10.1007/bf00961376

Cyclodimerization of a citral dienamine

- Summary
- Metrics

Abstract

The dienamine (a mixture of isomers) obtained from citral and diethylamine is converted to a mixture of citral anhydro cyclodimers by the action of weak proton-donor agents. The principal reaction product corresponds to [4 + 2]-cycloaddition of 1-diethylamino-7-methyl-3-methylene-1,6-octadiene (the minor component in the starting dienamine) to the enimmonium form of the protonated dienamine.

Related Organizations

Russian Academy of Sciences
Russian Federation

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).	0
	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