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Novel cyclization reactions on transition metal templates. The catalysis of intramolecular [4+2] cycloadditions by low-valent rhodium complexes

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This article is published in Journal of the American Chemical Society.The article was published on 1990-06-01. It has received 145 citations till now. The article focuses on the topics: Intramolecular reaction & Cycloaddition.

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The atom economy--a search for synthetic efficiency

TL;DR: Transition metal-catalyzed methods that are both selective and economical for formation of cyclic structures, of great interest for biological purposes, represent an important starting point for this long-term goal.
Journal ArticleDOI

Atomökonomische Synthesen – eine Herausforderung in der Organischen Chemie: die Homogenkatalyse als wegweisende Methode

TL;DR: In this paper, the Ubergangsmetall-komplexe, a komplexer organischer Verbindungen, are investigated, in which a grosen Zahl einfacher Additionsreaktionen and the Minimierung of Abfall-produkten erforderlich.
Journal ArticleDOI

Direct C−H Arylation of (Hetero)arenes with Aryl Iodides via Rhodium Catalysis

TL;DR: In this paper, a new method for the catalytic C−H arylation of heteroarenes and arenes that manifests high activity paired with reasonably broad scope was developed.
Journal ArticleDOI

Rh(III)-catalyzed C–H activation/[4 + 3] cycloaddition of benzamides and vinylcarbenoids: facile synthesis of azepinones

TL;DR: In this paper, a kinetic isotope effect study was conducted and a plausible mechanism was proposed for cycloaddition with benzamides to access azepinones, which makes a feature of simple starting materials, mild reaction conditions and high efficiency.
Journal ArticleDOI

Gold-Catalyzed [4C+2C] Cycloadditions of Allenedienes, including an Enantioselective Version with New Phosphoramidite-Based Catalysts: Mechanistic Aspects of the Divergence between [4C+3C] and [4C+2C] Pathways

TL;DR: Experimental and theoretical data dismiss a cationic mechanism involving intermediate II and suggest that the formation of the [4C+2C] cycloadducts might arise from a 1,2-alkyl migration (ring contraction) in a cycloheptenyl Au-carbene intermediate (IV), itself arising from a [ 4C+3C] concerted cycloaddition of the allenediene.
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