José Luis
Aceña Bonilla
Profesor/a Titular Universidad
![Foto de José Luis](/img/nophoto.png)
![Foto de Ikerbasque, Fundación Vasca para la Ciencia](/img/noimage_org.png)
Ikerbasque, Fundación Vasca para la Ciencia
Bilbao, EspañaPublicaciones en colaboración con investigadores/as de Ikerbasque, Fundación Vasca para la Ciencia (42)
2016
-
Advanced asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by alkylation/cyclization of newly designed axially chiral Ni(II) complex of glycine Schiff base
Amino Acids, Vol. 48, Núm. 4, pp. 973-986
-
Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II-III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas
Chemical Reviews, Vol. 116, Núm. 2, pp. 422-518
-
Small-Molecule Therapeutics for Ebola Virus (EBOV) Disease Treatment
European Journal of Organic Chemistry, Vol. 2016, Núm. 1, pp. 8-16
-
Tailor-Made α-Amino Acids in the Pharmaceutical Industry: Synthetic Approaches to (1R,2S)-1-Amino-2-vinylcyclopropane-1-carboxylic Acid (Vinyl-ACCA)
European Journal of Organic Chemistry, Vol. 2016, Núm. 16, pp. 2757-2774
2015
-
A comprehensive examination of the self-disproportionation of enantiomers (SDE) of chiral amides via achiral, laboratory-routine, gravity-driven column chromatography
RSC Advances, Vol. 5, Núm. 4, pp. 2988-2993
-
Asymmetric Synthesis of (2S,3S)-α-(1-Oxoisoindolin-3-yl)glycines under Low-Basicity "kinetic" Control
Journal of Organic Chemistry, Vol. 80, Núm. 22, pp. 11275-11280
-
Asymmetric carbon-carbon bond formation under solventless conditions in ball mills
ChemCatChem, Vol. 7, Núm. 8, pp. 1265-1269
-
Asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by sequential SN2-SN2′ dialkylation of (R)-N-(benzyl)proline-derived glycine Schiff base Ni(ii) complex
RSC Advances, Vol. 5, Núm. 2, pp. 1051-1058
-
Asymmetric synthesis of α-(1-oxoisoindolin-3-yl)glycine: Synthetic and mechanistic challenges
Chemical Communications, Vol. 51, Núm. 9, pp. 1624-1626
-
Carbonyl group coordination preferences in square-planar NiII and PdII complexes of pentadentate ligands by electron-withdrawing/donating substituents
Inorganica Chimica Acta, Vol. 433, pp. 3-12
-
Chemical Dynamic Thermodynamic Resolution and S/R Interconversion of Unprotected Unnatural Tailor-made α-Amino Acids
Journal of Organic Chemistry, Vol. 80, Núm. 20, pp. 9817-9830
-
Introducing a new radical trifluoromethylation reagent
Chemical Communications, Vol. 51, Núm. 27, pp. 5967-5970
-
Recent Progress in the in situ Detrifluoroacetylative Generation of Fluoro Enolates and Their Reactions with Electrophiles
European Journal of Organic Chemistry, Vol. 2015, Núm. 29, pp. 6401-6412
-
Synthesis of (2S,3S)-β-(trifluoromethyl)-α,β-diamino acid by Mannich addition of glycine Schiff base Ni(II) complexes to N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine
Journal of Fluorine Chemistry, Vol. 171, pp. 67-72
2014
-
Asymmetric Mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3- trifluoroacetaldimine and malonic acid derivatives. Stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids
Organic and Biomolecular Chemistry, Vol. 12, Núm. 9, pp. 1454-1462
-
Asymmetric synthesis of α-amino acids under operationally convenient conditions
Advanced Synthesis and Catalysis, Vol. 356, Núm. 10, pp. 2203-2208
-
Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations
Amino Acids, Vol. 46, Núm. 9, pp. 2047-2073
-
Chemical dynamic kinetic resolution and S/R interconversion of unprotected α-amino acids
Angewandte Chemie - International Edition, Vol. 53, Núm. 45, pp. 12214-12217
-
Chemical kinetic resolution of unprotected β-substituted β-amino acids using recyclable chiral ligands
Angewandte Chemie - International Edition, Vol. 53, Núm. 30, pp. 7883-7886
-
Chiral N(H)-tBu and N(H)-Ad NiII complexes of glycine schiff bases: Deduction of a mode of kinetic diastereoselectivity
European Journal of Organic Chemistry, Vol. 2014, Núm. 20, pp. 4309-4314