2015
DOI: 10.1002/chin.201501117
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Synthesis of 1,4‐Enamino Ketones by [3,3]‐Rearrangements of Dialkenylhydroxylamines.

Abstract: Synthesis of 1,4-Enamino Ketones by [3,3]-Rearrangements of Dialkenyl-hydroxylamines. -A new method for the synthesis of 1,4-enamino ketones through rearrangement of dialkenylhydroxylamines generated in situ by addition of N-alkenylnitrones to allenes is described. This route to dialkenylhydroxylamines has a broader scope than the Trofimov reaction. Additionally, the transformation of the obtained 1,4-enamino ketones to pyrroles, 1,4-diones, and furans is also shown. -(PECAK, W. H.; SON, J.; BURNSTINE, A. J.; … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?