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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Liebigs Annalenarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Liebigs Annalen
Article . 1996 . Peer-reviewed
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https://dx.doi.org/10.1002/jla...
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Polycyclic Aromatic Alkaloids, XI A Convenient Formal Total Synthesis of the Cytotoxic Marine Alkaloid Amphimedine

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 1996 English Publisher:WileyJournal:Liebigs Annalen, volume 1,996, pages 115-116 (issn: 0947-3440, Copyright policy )
Authors: Franz Bracher; Thomas Papke;

doi: 10.1002/jlac.199619960118

Polycyclic Aromatic Alkaloids, XI A Convenient Formal Total Synthesis of the Cytotoxic Marine Alkaloid Amphimedine

Abstract

AbstractThe pyridylbenzo[c][2,7]naphthyridinone 2, a central intermediate for the total synthesis of amphimedine (1), was prepared in two steps from the readily available quinoline 3. Palladium‐catalyzed cross‐coupling of 3 with 4‐(trimethylstannyl)pyridine gave the biarene 4, which could be converted to the target compound 2 by using a one‐pot anellation method.

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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).
BIP!Citations provided by BIP!
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.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
13
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