Argitalpenak (17) Carlos Tomás Nieto García argitalpenak

2024

  1. 2-Heteroarylethylamines in medicinal chemistry: a review of 2-phenethylamine satellite chemical space

    Beilstein Journal of Organic Chemistry, Vol. 20, pp. 1880-1893

2023

  1. (R)-N-Benzyl-N-(1-phenylethyl)cyclohexanamine

    MolBank, Vol. 2023, Núm. 1

  2. (S)-N1,N3-Dibenzyl-1-cyclohexyl-N1,N3-bis((R)-1-phenylethyl)propane-1,3-diamine

    MolBank, Vol. 2023, Núm. 1

  3. 2-Phenethylamines in Medicinal Chemistry: A Review

    Molecules, Vol. 28, Núm. 2

  4. Jugando con el benceno en la síntesis de feniletilaminas

    IX Jornadas de investigadoras de Castilla y León

2021

  1. Synthesis and modeling of ezetimibe analogues

    Molecules, Vol. 26, Núm. 11

2020

  1. Asymmetric Synthesis of 2,3,6-Trisubstituted Piperidines via Baylis-Hillman Adducts and Lithium Amide through Domino Reaction

    Synlett, Vol. 31, Núm. 6, pp. 600-604

2019

  1. 8.1.6 Product Subclass 6: Lithium Amides

    Knowledge Updates 2019/1

  2. Product subclass 6: Lithium amides

    Science of Synthesis, Vol. 2019, Núm. 1, pp. 65-179

2017

  1. Asymmetric synthesis of tert-butyl ((1R,4aR,8R,8aR)-1-hydroxyoctahydro-1H-isochromen-8-yl)carbamate

    Tetrahedron Asymmetry, Vol. 28, Núm. 10, pp. 1394-1400

2015

  1. Design, synthesis, pharmacological evaluation and molecular dynamics of β-amino acids morphan-derivatives as novel ligands for opioid receptors

    European Journal of Medicinal Chemistry, Vol. 101, pp. 150-162

2014

  1. Rapid access with diversity to enantiopure flexible PNA monomers following asymmetric orthogonal strategies

    Tetrahedron Asymmetry, Vol. 25, Núm. 13-14, pp. 1046-1060

  2. To be or not to be butterfly: New mechanistic insights in the Aza-Michael asymmetric addition of lithium (R)-N-benzyl-N-(α-methylbenzyl)amide

    Journal of Computational Chemistry, Vol. 35, Núm. 25, pp. 1846-1853

2013

  1. Enantioselective synthesis of a (1 R,5 R,9 R)-2-azabicyclo[33.1]nonane-9- carboxylic acid with an embedded morphan motif: A multipurpose product

    Synlett, Vol. 24, Núm. 2, pp. 169-172

2012

  1. 1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study

    Tetrahedron Asymmetry, Vol. 23, Núm. 1, pp. 76-85

  2. Erratum: 1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study (Tetrahedron: Asymmetry (2012) (76-85) DOI:10.1016/j.tetasy.2012.01.006)

    Tetrahedron Asymmetry

2010

  1. Potential of (2E,7E)-nonadienedioates in asymmetric synthesis: Construction of homopipecolic acid and an aminoester building block for peptide nucleic acids

    Synlett, pp. 587-590