Literature DB >> 22926995

A concise synthesis of (-)-aplyviolene facilitated by a strategic tertiary radical conjugate addition.

Martin J Schnermann1, Larry E Overman.   

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Year:  2012        PMID： 22926995      PMCID： PMC3517069          DOI： 10.1002/anie.201204977

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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2.  Enantioselective total synthesis of aplyviolene.

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7.  Reagent-controlled stereoselectivity in titanocene-catalyzed epoxide openings: reductions and intermolecular additions to alpha,beta-unsaturated carbonyl compounds.

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8.  Efficient visible light photocatalysis of [2+2] enone cycloadditions.

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9.  Scope and facial selectivity of the Prins-pinacol synthesis of attached rings.

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10.  Electron-transfer photoredox catalysis: development of a tin-free reductive dehalogenation reaction.

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Journal:  J Am Chem Soc       Date:  2009-07-01       Impact factor: 15.419
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  41 in total

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Review 4.  Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products.

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9.  Hydrodecarboxylation of Carboxylic and Malonic Acid Derivatives via Organic Photoredox Catalysis: Substrate Scope and Mechanistic Insight.

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10.  Enantioselective Synthesis of Vicinal All-Carbon Quaternary Centers via Iridium-Catalyzed Allylic Alkylation.

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