Literature DB >> 19847338

Bond formations by intermolecular and intramolecular trappings of acylketenes and their applications in natural product synthesis.

Keith P Reber1, S David Tilley, Erik J Sorensen.   

Abstract

The reactive intermediates known as acylketenes exhibit a rich chemistry and have been extensively utilized for many types of inter- and intramolecular bond-forming reactions within the field of organic synthesis. Characteristic reactions of acylketenes include cycloadditions, carbon-carbon bond-forming reactions, and nucleophilic capture with alcohols or amines to give beta-keto acid derivatives. In particular, the intramolecular capture of acylketene intermediates with pendant nucleophiles represents a powerful method for forming both medium-sized rings and macrocycles, often in high yield. This tutorial review examines the history, generation, and reactivity of acylketenes with a special focus on their applications in the synthesis of natural products.

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Year:  2009        PMID: 19847338      PMCID: PMC3227143          DOI: 10.1039/b912599j

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  17 in total

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  15 in total

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3.  Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions.

Authors:  Junjia Liu; Maurice A Marsini; T Aaron Bedell; Paul J Reider; Erik J Sorensen
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7.  Synthetic Studies to Lyngbouilloside: A Phosphate Tether-Mediated Synthesis of the Macrolactone Core.

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8.  Toward a synthesis of hirsutellone B by the concept of double cyclization.

Authors:  Keith P Reber; S David Tilley; Cheryl A Carson; Erik J Sorensen
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9.  Design and Synthesis of Molecular Scaffolds with Anti-infective Activity.

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10.  A Biocatalytic Route to Highly Enantioenriched β-Hydroxydioxinones.

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