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Diastereoselective carboxyl migrations of 3-arylbenzofuranones.

Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Research Abstract Details 

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  • Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Abstract Text:

    gorka perisGorka Peris,edwin vedejsEdwin Vedejs,gorka perisGorka Peris,edwin vedejsEdwin Vedejs,

    Mixed benzofuranyl carbonates derived from chiral chloroformates rearranged in the presence of nucleophilic catalysts to give C-carboxylated benzofurans with variable dr. The use of chiral nucleophilic catalysts gave modest improvement in dr, but better results were obtained by optimizing auxiliary and catalyst. Thus, 8k was obtained with 9:1 dr.

    Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Publishing Authors By Initials

    g perisG Peris,e vedejsE Vedejs,g perisG Peris,e vedejsE Vedejs,

    For similar abstracts research abstracts see: abstracts research

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    Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: The Journal of organic chemistry

    VOLUME: 73

    Page Numbers: 1158-61

    Journal Abbreviation: J. Org. Chem.

    ISSN: 0022-3263

    DAY: 8

    MONTH: 01

    YEAR: 2008

    Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 2985193

    Diastereoselective carboxyl migrations of 3-arylbenzofuranones. Keywords Mesh Terms:

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    Grant and Affiliation Information for Diastereoselective carboxyl migrations of 3-arylbenzofuranones.

    AFFILIATION: Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109 gorka.peris@yale.edu.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Org Chem

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