FRANCISCA
REBOLLEDO VICENTE
Catedrática de Universidad
Publicaciones en las que colabora con VICENTE MIGUEL GOTOR SANTAMARIA (65)
2013
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Chemoenzymatic synthesis of orthogonally protected (3R,4R)- and (3S,4S)-trans-3-amino-4-hydroxypyrrolidines
Tetrahedron, Vol. 69, Núm. 26, pp. 5407-5412
2012
2011
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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
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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
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An efficient chemoenzymatic method to prepare optically active primary-tertiary trans-cycloalkane-1,2-diamines
Tetrahedron, Vol. 65, Núm. 38, pp. 8028-8034
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Highly efficient chemoenzymatic syntheses of trans-2-aminocyclopentanol derivatives
Journal of Molecular Catalysis B: Enzymatic, Vol. 59, Núm. 1-3, pp. 111-115
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Trans-Cyclopentane-1,2-diamine: The second youth of the forgotten diamine
Chemical Society Reviews, Vol. 38, Núm. 7, pp. 1916-1925
2008
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An improved chemoenzymatic synthesis of both enantiomers of trans-cyclopentane-1,2-diamine
Tetrahedron Asymmetry, Vol. 19, Núm. 6, pp. 751-755
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Chemoenzymatic preparation of optically active anthracene derivatives
Tetrahedron Asymmetry, Vol. 19, Núm. 22, pp. 2589-2593
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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
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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
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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
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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
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Optically active trans-2-aminocyclopentanols: Chemoenzymatic preparation and application as chiral ligands
Biotechnology Journal, Vol. 1, Núm. 7-8, pp. 835-841
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Preparation of chiral pharmaceuticals through enzymatic acylation of alcohols and amines
Biocatalysis in the Pharmaceutical and Biotechnology Industries (CRC Press), pp. 203-248
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Redesigning the mechanism of the lipase-catalysed aminolysis of esters
Tetrahedron Asymmetry, Vol. 17, Núm. 8, pp. 1264-1274
2005
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Enantioselective acylation of rac-2-phenylcycloalkanamines catalyzed by lipases
Tetrahedron Asymmetry, Vol. 16, Núm. 18, pp. 3070-3076
2004
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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
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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
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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