4.7 Article

Stereoselective Formation of Alkenyl Halides via Magnesium Halide Promoted Ring Opening of Bis-Activated Cyclopropenes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 74, Issue 3, Pages 1353-1355

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo802475x

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Funding

  1. EaStCHEM (The Edinburgh and St. Andrews Research School of Chemistry)

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In the presence of stoichiometric magnesium halides, a range of bis-activated cyclopropenes undergo highly stereoselective ring-opening reactions to produce multi substituted alkenyl halides. More highly functionalized compounds may be obtained by trapping of the magnesium enolate intermediates in situ.

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