Journal ArticleDOI
Synthesis of 3-pyrrolines, annulated 3-pyrrolines, and pyrroles from alpha-amino allenes.
R K Dieter,H Yu +1 more
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TLDR
In this article, Palladium-catalyzed cyclization of α-amino allenes affords either the pyrroline or pyrrole depending on reaction conditions and provides for introduction of an aryl substituent at the C-3 position of the α-amerino allene.About:
This article is published in Organic Letters.The article was published on 2001-10-31. It has received 90 citations till now. The article focuses on the topics: Pyrroline & Propargyl.read more
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Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis
Journal ArticleDOI
Transition Metal-Mediated Synthesis of Monocyclic Aromatic Heterocycles
TL;DR: The present review is a transition metal-catalyzed synthesis of aromatic monocyclic heterocycles, aiming at achieving greater levels of molecular complexity and better functional group compatibilities in a convergent and atom economical fashions from readily accessible starting materials and under mild reaction conditions.
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Late transition metal-catalyzed hydroamination and hydroamidation.
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Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions
Fabio Bellina,Renzo Rossi +1 more
TL;DR: The methods used for the synthesis of vicinal diaryl-substituted pyrrole, pyrroline and pyrrolidine derivatives are reviewed in this article, which contains 461 references and summarizes bioactivity data of some of these compounds.
Journal ArticleDOI
Silver-mediated synthesis of heterocycles.
TL;DR: Ag(I)-Mediated Additions to Alkenes 3183 5.2.1.
References
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Journal ArticleDOI
Facile Enantioselective Synthesis of Propargylic Alcohols by Direct Addition of Terminal Alkynes to Aldehydes
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On the Nature of the "Copper Effect" in the Stille Cross-Coupling
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Chiral Allylic and Allenic Stannanes as Reagents for Asymmetric Synthesis
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Palladium-catalysed vinylation of organic halides under solid–liquid phase transfer conditions
TL;DR: In this article, the Heck-type reactions involving organic halides proceed readily at or near room temperature when performed under solid-liquid phase transfer conditions, and they are shown to be stable at room temperature.
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Highly stereospecific palladium-catalysed vinylation of vinylic halides under solid-liquid phase transfer conditions.
TL;DR: In this article, conjugated dienoates, dienones and dienals are obtained with high stereospecificity (⩾95%) and in high yields from the corresponding (E,E) and (Z) vinylic halides, and substrates (methyl acrylate, methyl vinyl ketone or acrolein).