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Stereoselective Multiple Bond-Forming Transformations (MBFTs): The Power of 1,2- and 1,3-Dicarbonyl Compounds

Authors

  • Dr. Damien Bonne,

    1. Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
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  • Prof. Dr. Thierry Constantieux,

    1. Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
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  • Dr. Yoann Coquerel,

    Corresponding author
    1. Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
    • Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
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  • Prof. Dr. Jean Rodriguez

    Corresponding author
    1. Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
    • Aix-Marseille Université, CNRS, iSm2, UMR 7313, Service 531, 13397 Marseille cedex 20 (France), Fax: (+33) 491-289-187
    Search for more papers by this author

Abstract

Although long known, 1,2- and 1,3-dicarbonyl compounds have recently come more and more to prevalence as ideal substrates for the invention of new stereoselective multiple bond-forming transformations (MBFTs). Herein, a critical appraisal is presented of some of the most spectacular of these MBFTs, which allow the formation from three up to six bonds in highly step- and atom-economical processes.

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