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Journal ArticleDOI

Periselective intramolecular cycloaddition of allene-1,3-dicarboxylates. Unusual structural feature of [2 + 2] cycloadducts

TLDR
In this article, a cycloaddition intramoleculaire de pentadienedioates de methyle and cyclohexene-2yle donne des derives de naphto [1,8-bc] pyranne and de cyclobuta [de] benzopyranne.
Abstract
La cycloaddition intramoleculaire de pentadienedioates de methyle et cyclohexene-2yle donne des derives de naphto [1,8-bc] pyranne et de cyclobuta [de] benzopyranne dont la structure est confirmee par analyse RX. Etude de l'effet des substituants sur les niveaux d'energie HOMO/LUMO de l'allene par methode AM1

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Journal ArticleDOI

A new allenic Pauson-Khand cycloaddition for the preparation of α-methylene cyclopentenones

TL;DR: Alkynyl allenes undergo an intramolecular molybdenum-mediated Pauson-Khand cycloaddition to provide functionalized α-methylene cyclopentenones in one step as discussed by the authors.
Journal ArticleDOI

Phenylsulfonyl ene-allenes as efficient precursors to bicyclic systems via intramolecular [2 + 2]-cycloaddition reactions.

TL;DR: Various phenylsulfonyl allene derivatives were prepared with double bonds tethered either to the alpha-position or the gamma-position of the allene, resulting in highly regio- and stereospecific thermal [2 + 2]-cycloaddition across the nonactivated cumulene double bond.
Journal ArticleDOI

Acid‐Catalyzed Intramolecular [2+2] Cycloaddition of Ene‐allenones: Facile Access to Bicyclo[n.2.0] Frameworks

TL;DR: A highly efficient acid-catalyzed intramolecular [2+2] cycloaddition between the distal allenic double bond and unactivated alkene moieties, with excellent chemo-, regio-, and diastereoselectivities under very mild reaction conditions is described.
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