Palladium-catalyzed N-arylation of 3-functionalized 2-amino-4,5- dimethylpyrroles
- Carlos P. Griswold,
- Nisaraporn Suthiwangcharoen,
- Steven M. Pochini,
- Chad E. Stephens
- Augusta University
Scholary Output:
Contribution to journal
Article
Peer-review
Open access
Abstract
A versatile class of 2-aminopyrroles containing various electron-withdrawing substituents at the 3-position have been N-arylated on the amine using a palladiumcatalyzed cross-coupling reaction. Using this methodology, a pyrimidone-based tricyclic system has been prepared in just one step from a starting 2-aminopyrrole.
Publication Information
Output type
Scholary Output:
Contribution to journal
Article
Peer-reviewOriginal language
English (US)Pages from-to (Number of pages)
Pages 1672-1681 (10 pages)Journal (Volume, Issue Number)
Synthetic Communications (Volume 41, Issue 11)Publication milestones
- Published - 2011
Publication status
Published - 2011
ISSN
0039-7911Publication IDs
- Scopus: 79955681048
Publication metrics
Metrics
SciVal
citations
2
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1
SciVal
FWCI
0.10
SciVal
Author count
4
SciVal
Paper percentile
40
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Citation count
3
Captures
4
Funding Details
We thank our department and the Pamplin College of Arts and Sciences for funding of this research.