JOSE LUIS ACEÑA BONILLA-rekin lankidetzan egindako argitalpenak (43)

2016

  1. 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

  2. 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

  3. Small-Molecule Therapeutics for Ebola Virus (EBOV) Disease Treatment

    European Journal of Organic Chemistry, Vol. 2016, Núm. 1, pp. 8-16

  4. 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

  1. 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

  2. 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

  3. Asymmetric carbon-carbon bond formation under solventless conditions in ball mills

    ChemCatChem, Vol. 7, Núm. 8, pp. 1265-1269

  4. 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

  5. Asymmetric synthesis of α-(1-oxoisoindolin-3-yl)glycine: Synthetic and mechanistic challenges

    Chemical Communications, Vol. 51, Núm. 9, pp. 1624-1626

  6. 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

  7. 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

  8. Introducing a new radical trifluoromethylation reagent

    Chemical Communications, Vol. 51, Núm. 27, pp. 5967-5970

  9. 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

  10. 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

  1. 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

  2. Asymmetric synthesis of α-amino acids under operationally convenient conditions

    Advanced Synthesis and Catalysis, Vol. 356, Núm. 10, pp. 2203-2208

  3. 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

  4. Chemical dynamic kinetic resolution and S/R interconversion of unprotected α-amino acids

    Angewandte Chemie - International Edition, Vol. 53, Núm. 45, pp. 12214-12217

  5. 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

  6. 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