Articles producció científicaQuímica Analítica i Química Orgànica

Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization

  • Identification data

    Identifier:  imarina:9440801
    Handle: https://hdl.handle.net/20.500.11797/imarina9440801
    Authors:  Homs, A; Muratore, ME; Echavarren, AM
    Abstract:
    The first enantioselective total synthesis of (-)-nardoaristolone B is accomplished by the implementation of an enantio- and diastereoselective copper(I)-catalyzed conjugate addition/enolate trapping sequence and a gold(I)-catalyzed oxidative cyclization (intermolecular oxidant), employed for the first time in total synthesis.

  • Others:

    Link to the original source: https://pubs.acs.org/doi/full/10.1021/ol503531n
    APA: Homs, A; Muratore, ME; Echavarren, AM (2015). Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization. Organic Letters, 17(3), 461-463. DOI: 10.1021/ol503531n
    Paper original source: Organic Letters. 17 (3): 461-463
    Article's DOI: 10.1021/ol503531n
    Journal publication year: 2015-02-06
    Entity: Universitat Rovira i Virgili
    Paper version: info:eu-repo/semantics/publishedVersion
    Record's date: 2026-05-09
    URV's Author/s: ECHAVARREN PABLOS, ANTONIO
    Department: Química Analítica i Química Orgànica
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Publication Type: Journal Publications
    Author, as appears in the article.: Homs, A; Muratore, ME; Echavarren, AM
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Thematic Areas: Physical and theoretical chemistry, Organic chemistry, General medicine, Chemistry, organic, Biotecnología, Biodiversidade, Biochemistry
    Author's mail: antoniomaria.echavarren@urv.cat, antoniomaria.echavarren@urv.cat

  • Keywords:

    Reagents
    Constructio
    Asymmetric conjugate addition
    Biochemistry
    Chemistry
    Organic
    Organic Chemistry
    Physical and Theoretical Chemistry
    General medicine
    Biotecnología
    Biodiversidade

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