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“Isocyanide-free” Ugi reactions

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2009 France English Publisher:Royal Society of Chemistry (RSC)Journal:Organic & Biomolecular Chemistry, volume 7, page 3,024 (issn: 1477-0520, eissn: 1477-0539, Copyright policy )
Authors: El Kaim, Laurent; Grimaud, Laurence; Schiltz, Aurelie;

doi: 10.1039/b908541f

“Isocyanide-free” Ugi reactions

Abstract

High-yielding Ugi reactions have been carried out with in situ-prepared isocyanides, derived from the reaction of bromide derivatives with silver and potassium cyanide, thus alleviating the burden of the preparation, purification and subsequent use of isocyanides in multicomponent reactions.

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France
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[CHIM.ORGA]Chemical Sciences/Organic chemistry

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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!
32
Top 10%
Top 10%
Top 10%
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