articleTop 1% cited
3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches
European Journal of Organic Chemistry · 2010 · Vol. 2010(24) · pp. 4527–4547
Alessia Millemaggi(University of York)Richard J. K. Taylor✉(University of York)
Abstract
Abstract The structures and biological activities of naturally occurring 3‐alkenyl‐oxindoles are reviewed. Important man‐made3‐alkenyl‐oxindoles are covered, particularly those with pharmaceutical applications such as sunitinib (SU11248), the orally active receptor tyrosine kinase inhibitor marketed by Pfizer as Sutent ® . Traditional synthetic approaches to 3‐alkenyl‐oxindoles are summarised and then recently developed tandem/telescoped synthetic routes are described.
Synthetic Organic Chemistry MethodsAsymmetric Synthesis and CatalysisChemical Synthesis and AnalysisChemistryTandemCombinatorial chemistry
Funding
- Engineering and Physical Sciences Research Council
Citations
361
FWCI
12.29
field-weighted impact
References
104
Percentile
99%
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Citations per year
Cited by
Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation
European Journal of Organic Chemistry · 2011 · 309 citations
References
Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids
European Journal of Organic Chemistry · 2003 · 1,435 citations
Multicomponent Reactions with Isocyanides
Angewandte Chemie International Edition · 2000 · 4,022 citations
Pyrrolidinyl‐Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
Angewandte Chemie International Edition · 2007 · 2,393 citations
Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
Synthesis · 2009 · 1,062 citations
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