Publicaciones en las que colabora con IVAN LAVANDERA GARCIA (60)

2018

  1. Mild Chemoenzymatic Oxidation of Allylic sec-Alcohols. Application to Biocatalytic Stereoselective Redox Isomerizations

    ACS Catalysis, Vol. 8, Núm. 3, pp. 2413-2419

2017

  1. Novel chemoenzymatic oxidation of amines into oximes based on hydrolase-catalysed peracid formation

    Organic and Biomolecular Chemistry, Vol. 15, Núm. 15, pp. 3196-3201

  2. Stereoselective amination of racemic sec-alcohols through sequential application of laccases and transaminases

    Green Chemistry, Vol. 19, Núm. 2, pp. 474-480

  3. Synthesis of nitrogenated lignin-derived compounds and reactivity with laccases. Study of their application in mild chemoenzymatic oxidative processes

    RSC Advances, Vol. 7, Núm. 80, pp. 50459-50471

2016

  1. Baeyer–Villiger monooxygenase-catalyzed desymmetrizations of cyclobutanones. Application to the synthesis of valuable spirolactones

    Tetrahedron, Vol. 72, Núm. 46, pp. 7268-7275

  2. But-2-ene-1,4-diamine and But-2-ene-1,4-diol as Donors for Thermodynamically Favored Transaminase- and Alcohol Dehydrogenase-Catalyzed Processes

    Advanced Synthesis and Catalysis, Vol. 358, Núm. 10, pp. 1618-1624

  3. Catalytic Promiscuity of Transaminases: Preparation of Enantioenriched β-Fluoroamines by Formal Tandem Hydrodefluorination/Deamination

    Angewandte Chemie - International Edition, Vol. 55, Núm. 9, pp. 3144-3147

2015

  1. Broadening the chemical scope of laccases: Selective deprotection of N-benzyl groups

    Green Chemistry, Vol. 17, Núm. 5, pp. 2794-2798

  2. Chemoenzymatic Deracemization of Secondary Alcohols by using a TEMPO-Iodine-Alcohol Dehydrogenase System

    ChemCatChem, Vol. 7, Núm. 24, pp. 4016-4020

  3. Deracemisation of profenol core by combining laccase/TEMPO-mediated oxidation and alcohol dehydrogenase-catalysed dynamic kinetic resolution

    Catalysis Science and Technology, Vol. 5, Núm. 3, pp. 1443-1446

2014

  1. Asymmetric chemoenzymatic synthesis of N-acetyl-α-amino esters based on lipase-catalyzed kinetic resolutions through interesterification reactions

    Tetrahedron, Vol. 70, Núm. 13, pp. 2264-2271

  2. Expanding the scope of alcohol dehydrogenases towards bulkier substrates: Stereo- and enantiopreference for α,α-dihalogenated ketones

    ChemCatChem, Vol. 6, Núm. 4, pp. 1066-1072

  3. Imidazolium-based ionic liquids as non-conventional media for alcohol dehydrogenase-catalysed reactions

    Topics in Catalysis, Vol. 57, Núm. 5, pp. 332-338

  4. Laccase/2,2,6,6-tetramethylpiperidinoxyl radical (TEMPO): An efficient catalytic system for selective oxidations of primary hydroxy and amino groups in aqueous and biphasic media

    Advanced Synthesis and Catalysis, Vol. 356, Núm. 10, pp. 2321-2329

  5. Laccase/TEMPO-mediated system for the thermodynamically disfavored oxidation of 2,2-dihalo-1-phenylethanol derivatives

    Green Chemistry, Vol. 16, Núm. 5, pp. 2448-2453

  6. Regioselective preparation of thiamphenicol esters through lipase-catalyzed processes

    Journal of the Brazilian Chemical Society, Vol. 25, Núm. 6, pp. 987-994

  7. Stereodivergent preparation of valuable γ- Or δ-hydroxy esters and lactones through one-pot cascade or tandem chemoenzymatic protocols

    ACS Catalysis, Vol. 4, Núm. 2, pp. 386-393

  8. Steric vs. electronic effects in the Lactobacillus brevis ADH-catalyzed bioreduction of ketones

    Organic and Biomolecular Chemistry, Vol. 12, Núm. 4, pp. 673-681

  9. Transaminases applied to the synthesis of high added-value enantiopure amines

    Organic Process Research and Development, Vol. 18, Núm. 6, pp. 788-792

2013

  1. Biocatalyzed synthesis of both enantiopure fluoromisonidazole antipodes

    Tetrahedron Letters, Vol. 54, Núm. 37, pp. 5022-5025