Publicaciones en las que colabora con FRANCISCA REBOLLEDO VICENTE (64)

2013

  1. Chemoenzymatic synthesis of orthogonally protected (3R,4R)- and (3S,4S)-trans-3-amino-4-hydroxypyrrolidines

    Tetrahedron, Vol. 69, Núm. 26, pp. 5407-5412

2012

  1. Chemoenzymatic preparation of optically active trans- and cis-cyclohex-4-ene-1,2-diamine and trans-6-aminocyclohex-3-enol derivatives

    Tetrahedron

2011

  1. Straightforward preparation of biologically active 1-aryl- and 1-heteroarylpropan-2-amines in enantioenriched form

    Organic and Biomolecular Chemistry, Vol. 9, Núm. 7, pp. 2274-2278

2010

  1. Enzymatic dynamic kinetic resolution of (±)-cis-N-(Alkoxycarbonyl) cyclopentane-1,2-diamines based on spontaneous racemization

    Organic Letters, Vol. 12, Núm. 16, pp. 3602-3605

2009

  1. An efficient chemoenzymatic method to prepare optically active primary-tertiary trans-cycloalkane-1,2-diamines

    Tetrahedron, Vol. 65, Núm. 38, pp. 8028-8034

  2. Highly efficient chemoenzymatic syntheses of trans-2-aminocyclopentanol derivatives

    Journal of Molecular Catalysis B: Enzymatic, Vol. 59, Núm. 1-3, pp. 111-115

  3. Trans-Cyclopentane-1,2-diamine: The second youth of the forgotten diamine

    Chemical Society Reviews, Vol. 38, Núm. 7, pp. 1916-1925

2008

  1. An improved chemoenzymatic synthesis of both enantiomers of trans-cyclopentane-1,2-diamine

    Tetrahedron Asymmetry, Vol. 19, Núm. 6, pp. 751-755

  2. Chemoenzymatic preparation of optically active anthracene derivatives

    Tetrahedron Asymmetry, Vol. 19, Núm. 22, pp. 2589-2593

  3. Cycloalkane-1,2-diamine derivatives as chiral solvating agents. Study of the structural variables controlling the NMR enantiodiscrimination of chiral carboxylic acids

    Tetrahedron, Vol. 64, Núm. 33, pp. 7709-7717

2007

  1. A biocatalytic approach to synthesizing optically active orthogonally protected trans-cyclopentane-1,2-diamine derivatives

    Journal of Organic Chemistry, Vol. 72, Núm. 4, pp. 1309-1314

  2. New pincer-like receptor derived from trans-cyclopentane-1,2-diamine as a chiral shift reagent for carboxylic acids

    Tetrahedron Asymmetry, Vol. 18, Núm. 16, pp. 1981-1985

2006

  1. Chemoenzymatic syntheses of novel ligands derived from trans-cyclohexane-1, 2-diamine: Application in the enantioselective addition of diethylzinc to aromatic aldehydes

    Tetrahedron Asymmetry, Vol. 17, Núm. 3, pp. 449-454

  2. Optically active trans-2-aminocyclopentanols: Chemoenzymatic preparation and application as chiral ligands

    Biotechnology Journal, Vol. 1, Núm. 7-8, pp. 835-841

  3. Preparation of chiral pharmaceuticals through enzymatic acylation of alcohols and amines

    Biocatalysis in the Pharmaceutical and Biotechnology Industries (CRC Press), pp. 203-248

  4. Redesigning the mechanism of the lipase-catalysed aminolysis of esters

    Tetrahedron Asymmetry, Vol. 17, Núm. 8, pp. 1264-1274

2005

  1. Enantioselective acylation of rac-2-phenylcycloalkanamines catalyzed by lipases

    Tetrahedron Asymmetry, Vol. 16, Núm. 18, pp. 3070-3076

2004

  1. Chemoenzymatic preparation of optically active trans-cyclohexane-1,2- diamine derivatives: An efficient synthesis of the analgesic U-(-)-50,488

    Chemistry - A European Journal, Vol. 10, Núm. 22, pp. 5788-5794

  2. Chemoenzymatic preparation of optically active β-amino-cyclohexanols and their application in the enantioselective addition of diethylzinc to benzaldehyde

    Tetrahedron Asymmetry, Vol. 15, Núm. 8, pp. 1335-1341

  3. Kinetic resolution of (±)-trans- and (±)-cis-2- phenylcyclopentanamine by CALB-catalyzed aminolysis of esters: The key role of the leaving group

    Tetrahedron Asymmetry, Vol. 15, Núm. 3, pp. 481-488