Publicacions en què col·labora amb Vito Capriati (21)

2024

  1. Recent Advancements in the Utilization of s-Block Organometallic Reagents in Organic Synthesis with Sustainable Solvents

    Molecules, Vol. 29, Núm. 7

2023

  1. Cu-catalysed Chan-Evans-Lam reaction meets deep eutectic solvents: efficient and selective C-N bond formation under aerobic conditions at room temperature

    RSC Sustainability, Vol. 1, Núm. 4, pp. 847-852

  2. Deep eutectic solvents and heterogeneous catalysis with metallic nanoparticles: A powerful partnership in sustainable synthesis

    Current Opinion in Green and Sustainable Chemistry, Vol. 39

  3. From oximes to tertiary alcohols in water, at room temperature and under air: a hybrid one-pot tandem assembly of enzymatic deoximation and RLi/RMgX reagents

    Organic and Biomolecular Chemistry, Vol. 21, Núm. 21, pp. 4414-4421

2022

  1. Green Solvents for Eco-Friendly Synthesis of Dimethindene: A Forward-Looking Approach

    Molecules, Vol. 27, Núm. 21

  2. Ligand-Free Copper-Catalyzed Ullmann-Type C−O Bond Formation in Non-Innocent Deep Eutectic Solvents under Aerobic Conditions

    ChemSusChem, Vol. 15, Núm. 1

  3. Selective Aerobic Oxidation of Alcohols in Low Melting Mixtures and Water and Use for Telescoped One-Pot Hybrid Reactions

    ChemistryOpen, Vol. 11, Núm. 10, pp. e202200160

  4. Sustainable and Scalable Two-Step Synthesis of Thenfadil and Some Analogs in Deep Eutectic Solvents: From Laboratory to Industry

    ACS Sustainable Chemistry and Engineering, Vol. 10, Núm. 13, pp. 4065-4072

2021

  1. A Fast and General Route to Ketones from Amides and Organolithium Compounds under Aerobic Conditions: Synthetic and Mechanistic Aspects

    Chemistry - A European Journal, Vol. 27, Núm. 8, pp. 2868-2874

  2. A one-pot two-step synthesis of tertiary alcohols combining the biocatalytic laccase/TEMPO oxidation system with organolithium reagents in aerobic aqueous media at room temperature

    Chemical Communications, Vol. 57, Núm. 99, pp. 13534-13537

  3. Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions

    Organic and Biomolecular Chemistry, Vol. 19, Núm. 8, pp. 1773-1779

  4. Expeditious and practical synthesis of tertiary alcohols from esters enabled by highly polarized organometallic compounds under aerobic conditions in Deep Eutectic Solvents or bulk water

    Tetrahedron, Vol. 81

2020

  1. Addition of Highly Polarized Organometallic Compounds to N-tert-Butanesulfinyl Imines in Deep Eutectic Solvents under Air: Preparation of Chiral Amines of Pharmaceutical Interest

    ChemSusChem, Vol. 13, Núm. 14, pp. 3583-3588

  2. Deep eutectic solvent-catalyzed Meyer-Schuster rearrangement of propargylic alcohols under mild and bench reaction conditions

    Chemical Communications, Vol. 56, Núm. 96, pp. 15165-15168

  3. Fast and Chemoselective Addition of Highly Polarized Lithium Phosphides Generated in Deep Eutectic Solvents to Aldehydes and Epoxides

    ChemSusChem, Vol. 13, Núm. 18, pp. 4967-4973

2019

  1. Directed: Ortho-metalation-nucleophilic acyl substitution strategies in deep eutectic solvents: The organolithium base dictates the chemoselectivity

    Chemical Communications, Vol. 55, Núm. 54, pp. 7741-7744

2018

  1. Programming cascade reactions interfacing biocatalysis with transition-metal catalysis in: Deep Eutectic Solvents as biorenewable reaction media

    Green Chemistry, Vol. 20, Núm. 15, pp. 3468-3475

  2. The Future of Polar Organometallic Chemistry Written in Bio-Based Solvents and Water

    Chemistry - A European Journal, Vol. 24, Núm. 56, pp. 14854-14863

2017

  1. One-pot sustainable synthesis of tertiary alcohols by combining ruthenium-catalysed isomerisation of allylic alcohols and chemoselective addition of polar organometallic reagents in deep eutectic solvents

    Green Chemistry, Vol. 19, Núm. 13, pp. 3069-3077

2015

  1. Reactivity of Polar Organometallic Compounds in Unconventional Reaction Media: Challenges and Opportunities

    European Journal of Organic Chemistry, Vol. 2015, Núm. 31, pp. 6779-6799