Search Results - "de Lucca Jr, Emilio"

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  1. 1

    Chemoselective methylene oxidation in aromatic molecules by Zhao, Jinpeng, Nanjo, Takeshi, de Lucca, Emilio C., White, M. Christina

    Published in Nature chemistry (01-03-2019)
    “…Despite significant progress in the development of site-selective aliphatic C–H oxidations over the past decade, the ability to oxidize strong methylene C–H…”
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    Journal Article
  2. 2

    Enantioselective Synthesis of Phthalides and Isochromanones via Heck–Matsuda Arylation of Dihydrofurans by Kattela, Shivashankar, de Lucca, Emilio C., Correia, Carlos Roque D.

    Published in Chemistry : a European journal (03-12-2018)
    “…In this communication, the enantioselective synthesis of phthalides and isochromanones is described through a new palladium‐catalyzed Heck–Matsuda…”
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  3. 3
  4. 4

    Remote, Late-Stage Oxidation of Aliphatic C–H Bonds in Amide-Containing Molecules by Nanjo, Takeshi, de Lucca, Emilio C, White, M. Christina

    Published in Journal of the American Chemical Society (18-10-2017)
    “…Amide-containing molecules are ubiquitous in natural products, pharmaceuticals, and materials science. Due to their intermediate electron-richness, they are…”
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  5. 5

    Total Synthesis of (−)-Marinisporolide C by Dias, Luiz C, de Lucca, Emilio C

    Published in Journal of organic chemistry (17-03-2017)
    “…The first total synthesis of (−)-marinisporolide C is described, which establishes unequivocally the relative and absolute configuration of this oxopolyene…”
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  6. 6

    Selective Oxidations in the Synthesis of Complex Natural ent-Kauranes and ent-Beyeranes by Santana, Victor C. S., Rocha, Eduardo C. S., Pavan, Julian C. S., Heleno, Vladimir C. G., de Lucca, Emilio C.

    Published in Journal of organic chemistry (05-08-2022)
    “…Syntheses of two natural products derived from the ent-kaurene kaurenoic acid are described for the first time using regio- and diastereoselective oxidations…”
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  7. 7

    Total Synthesis of the Oxopolyene Macrolide (−)-Marinisporolide C by Dias, Luiz C., de Lucca, Emílio C.

    Published in Organic letters (18-12-2015)
    “…The first total synthesis of (−)-marinisporolide C was performed in 25 steps (longest linear sequence) and an overall yield of 1%. Due to the high degree of…”
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  8. 8

    The Role of β-Bulky Substituents in Aldol Reactions of Boron Enolates of Methylketones with Aldehydes: Experimental and Theoretical Studies by DFT Analysis by Dias, Luiz C, de Lucca, Emílio C, Ferreira, Marco A. B, Garcia, Danilo C, Tormena, Cláudio F

    Published in Journal of organic chemistry (17-02-2012)
    “…In this work, we show the influence of the volume of the β-substituents on the levels of 1,5-stereoselectivities of aldol reactions of boron enolates generated…”
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  9. 9

    Influence of β-Substituents in Aldol Reactions of Boron Enolates of β-Alkoxy Methylketones by Dias, Luiz C, de Lucca, Emílio C, Ferreira, Marco A. B, Garcia, Danilo C, Tormena, Cláudio F

    Published in Organic letters (05-11-2010)
    “…Moderate to good levels of substrate-based 1,5-syn-stereocontrol could be achieved in the boron-mediated aldol reactions of β-tert-butyl methylketones with…”
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  10. 10

    Metal-catalyzed asymmetric aldol reactions by Dias, Luiz C., Lucca Jr, Emílio C. de, Ferreira, Marco A. B., Polo, Ellen C.

    Published in Journal of the Brazilian Chemical Society (01-12-2012)
    “…The aldol reaction is one of the most powerful and versatile methods for the construction of C-C bonds. Traditionally, this reaction was developed in a…”
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