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Organoaluminum-promoted Claisen rearrangement of allyl vinyl ethers

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TLDR
Le (bis-[(bromo-4 di-t-butyl-2,6)phenoxy methyl) aluminium peut etre utilise pour obtenir l'isomere (Z) alors que l'sisomeres (E) est produit avec le (bis-(diphenyl 2,6 phenoxy] methyl) aluminum as discussed by the authors.
Abstract
Le (bis-[(bromo-4 di-t-butyl-2,6)phenoxy methyl) aluminium peut etre utilise pour obtenir l'isomere (Z) alors que l'isomere (E) est produit avec le (bis-[diphenyl-2,6 phenoxy] methyl) aluminium

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Journal ArticleDOI

Tandem [4+2]/[3+2] Cycloadditions of Nitroalkenes.

TL;DR: Denmark et al. as mentioned in this paper proposed a method to match the change in molecular complexity at each step with reactions of comparable synthetic complexity, which is a necessary condition for high synthetic efficiency.
Journal ArticleDOI

Gold(I)-Catalyzed Propargyl Claisen Rearrangement

TL;DR: Homoallenic alcohols are prepared from propargyl vinyl ethers using a trinuclear gold(I)-oxo complex, [(Ph3PAu)3O]BF4, as a catalyst for Propargyl Claisen rearrangement at room temperature with excellent diastereoselectivity and excellent chirality transfer.
Journal ArticleDOI

Propargyl Claisen rearrangement: allene synthesis and beyond

TL;DR: The correct use of appropriate propargyl vinyl ethers as starting materials coupled with suitable reaction conditions can aid in the development of new domino methodologies in which the allenes are valuable intermediates in route to a wide range of important classes of organic compounds.
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