IVAN
LAVANDERA GARCIA
Profesor Titular de Universidad
Publicaciones en las que colabora con VICENTE MIGUEL GOTOR SANTAMARIA (60)
2018
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Mild Chemoenzymatic Oxidation of Allylic sec-Alcohols. Application to Biocatalytic Stereoselective Redox Isomerizations
ACS Catalysis, Vol. 8, Núm. 3, pp. 2413-2419
2017
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Novel chemoenzymatic oxidation of amines into oximes based on hydrolase-catalysed peracid formation
Organic and Biomolecular Chemistry, Vol. 15, Núm. 15, pp. 3196-3201
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Stereoselective amination of racemic sec-alcohols through sequential application of laccases and transaminases
Green Chemistry, Vol. 19, Núm. 2, pp. 474-480
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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
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Baeyer–Villiger monooxygenase-catalyzed desymmetrizations of cyclobutanones. Application to the synthesis of valuable spirolactones
Tetrahedron, Vol. 72, Núm. 46, pp. 7268-7275
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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
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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
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Broadening the chemical scope of laccases: Selective deprotection of N-benzyl groups
Green Chemistry, Vol. 17, Núm. 5, pp. 2794-2798
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Chemoenzymatic Deracemization of Secondary Alcohols by using a TEMPO-Iodine-Alcohol Dehydrogenase System
ChemCatChem, Vol. 7, Núm. 24, pp. 4016-4020
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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
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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
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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
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Imidazolium-based ionic liquids as non-conventional media for alcohol dehydrogenase-catalysed reactions
Topics in Catalysis, Vol. 57, Núm. 5, pp. 332-338
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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
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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
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Regioselective preparation of thiamphenicol esters through lipase-catalyzed processes
Journal of the Brazilian Chemical Society, Vol. 25, Núm. 6, pp. 987-994
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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
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Steric vs. electronic effects in the Lactobacillus brevis ADH-catalyzed bioreduction of ketones
Organic and Biomolecular Chemistry, Vol. 12, Núm. 4, pp. 673-681
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Transaminases applied to the synthesis of high added-value enantiopure amines
Organic Process Research and Development, Vol. 18, Núm. 6, pp. 788-792
2013
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Biocatalyzed synthesis of both enantiopure fluoromisonidazole antipodes
Tetrahedron Letters, Vol. 54, Núm. 37, pp. 5022-5025