Publicacións (40) Publicacións nas que participase algún/ha investigador/a

filter_list Catalysis

2015

  1. Simplified NMR Procedures for the Assignment of the Absolute Configuration

    Structure Elucidation in Organic Chemistry: The Search for the Right Tools (Wiley Blackwell), pp. 241-278

2014

  1. Designing chiral derivatizing agents (CDA) for the NMR assignment of the absolute configuration: A theoretical and experimental approach with thiols as a case study

    Tetrahedron

2012

  1. Indium-mediated aza-Henry reaction of imines: Access to 2-nitroamines

    European Journal of Organic Chemistry, pp. 4339-4346

  2. Preparation of sugar derived β,β′-dihydroxy α,α-disubstituted α-amino acids

    Tetrahedron Asymmetry, Vol. 23, Núm. 17, pp. 1238-1242

  3. Synthesis of (1α)-1,25-dihydroxyvitamin D 3 with a β-positioned seven-carbon side chain at C(12)

    Helvetica Chimica Acta, Vol. 95, Núm. 10, pp. 1842-1850

2010

  1. 13C NMR as a general tool for the assignment of absolute configuration

    Chemical Communications, Vol. 46, Núm. 42, pp. 7903-7905

  2. Chiral 1, 2-Diols: The assignment of their absolute configuration by NMR made easy

    Organic Letters, Vol. 12, Núm. 2, pp. 208-211

  3. Dynamics of chitosan by 1H NMR relaxation

    Biomacromolecules, Vol. 11, Núm. 8, pp. 2079-2086

  4. Studies on the stereocontrolled transformation of nitrohexofuranoses into 2-oxabicyclo[2.2.1]heptanes. V: Synthesis of enantiopure methyl (1R,2R,4S)-2-amino-4-hydroxycyclopentanecarboxylate

    Tetrahedron Asymmetry, Vol. 21, Núm. 1, pp. 116-122

  5. Studies on the transformation of nitrosugars into iminosugars III: synthesis of (2R,3R,4R,5R,6R)-2-(hydroxymethyl)azepane-3,4,5,6-tetraol and (2R,3R,4R,5R,6S)-2-(hydroxymethyl)azepane-3,4,5,6-tetraol

    Tetrahedron Asymmetry, Vol. 21, Núm. 1, pp. 21-26

  6. Synthesis and biological evaluation of 6-methyl analog of 1α,25-dihydroxyvitamin D3

    Journal of Steroid Biochemistry and Molecular Biology, Vol. 121, Núm. 1-2, pp. 29-33

  7. The use of a single derivative in the configurational assignment of ketone cyanohydrins

    European Journal of Organic Chemistry, pp. 6520-6524

2009

  1. Absolute configuration of ketone cyanohydrins by 1H nmr: The special case of polar substituted tertiary alcohols

    Organic Letters, Vol. 11, Núm. 1, pp. 53-56

  2. Carbon-branched carbohydrate chirons: synthesis of C-3 and C-4-branched sugar lactones derived from d-erythronolactone

    Tetrahedron Asymmetry, Vol. 20, Núm. 20, pp. 2357-2367

  3. Doubly carbon-branched pentoses: synthesis of both enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection

    Tetrahedron Letters, Vol. 50, Núm. 36, pp. 5088-5093

  4. Stereocontrolled transformation of nitrohexofuranoses into cyclopentylamines via 2-oxabicyclo[2.2.1]heptanes. IV: Synthesis of enantiopure methyl (1S,2R,3R,4R,5S)-5-benzyloxycarbonylamino-2,3-isopropylidenedioxy-4-methoxycyclopentanecarboxylate

    Tetrahedron Asymmetry, Vol. 20, Núm. 6-8, pp. 892-896

  5. The stereochemistry of 1,2,3-triols revealed by 1H NMR spectroscopy: Principles and applications

    Chemistry - A European Journal, Vol. 15, Núm. 44, pp. 11963-11975

2008

  1. Assigning the configuration of amino alcohols by NMR: A single derivatization method

    Organic Letters, Vol. 10, Núm. 13, pp. 2733-2736

  2. Cross interaction between auxiliaries: The chirality of amino alcohols by NMR

    Organic Letters, Vol. 10, Núm. 13, pp. 2729-2732

  3. Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy

    Journal of Organic Chemistry, Vol. 73, Núm. 15, pp. 5714-5722