Publikationen, an denen er mitarbeitet MARIA OLGA CAAMAÑO SANTOS (57)

2013

  1. Synthesis and allosteric modulation of the dopamine receptor by peptide analogs of l-prolyl-l-leucyl-glycinamide (PLG) modified in the l-proline or l-proline and l-leucine scaffolds

    European Journal of Medicinal Chemistry, Vol. 69, pp. 146-158

2010

  1. A 'click chemistry' approach to the straightforward synthesis of new 4-aryl-1,2,3-triazolocarbanucleosides

    Arkivoc, Vol. 2010, Núm. 3, pp. 152-168

  2. Synthesis and pharmacological evaluation of novel 1,3,8- and 1,3,7,8-substituted xanthines as adenosine receptor antagonists

    Bioorganic and Medicinal Chemistry, Vol. 18, Núm. 5, pp. 2001-2009

  3. Synthesis of methyl (±)-3,5-bis(substitutedmethyl)pyrrolidine-2- carboxylates: A convenient approach to proline-mimetics

    Tetrahedron, Vol. 66, Núm. 34, pp. 6797-6805

2009

  1. 1,3-Dialkyl-8-N-substituted benzyloxycarbonylamino-9-deazaxanthines as potent adenosine receptor ligands: Design, synthesis, structure-affinity and structure-selectivity relationships

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 10, pp. 3618-3629

  2. Synthesis and biological evaluation of 6-substituted purinylcarbanucleosides with a cyclopenta[b]thiophene pseudosugar

    Synthesis, pp. 2766-2772

  3. Synthesis and pharmacological evaluation of novel 1- and 8-substituted-3-furfuryl xanthines as adenosine receptor antagonists

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 18, pp. 6755-6760

  4. Synthesis of novel 1-alkyl-8-substituted-3-(3-methoxypropyl) xanthines as putative A2B receptor antagonists

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 9, pp. 3426-3432

2008

  1. Synthesis and antiviral activities of novel purinyl- and pyrimidinyl-carbanucleosides derived from indan

    Synthesis, pp. 1845-1852

  2. Synthesis of novel purinyl-1′-homocarbanucleosides based on a cyclopenta[b]pyrazine system

    Chemical and Pharmaceutical Bulletin, Vol. 56, Núm. 5, pp. 654-658

2007

  1. Cyclocondensation of (±)-exo,exo-5,6-(isopropylidenedioxy)-3- (pyrrolidino-methylene)bicyclo[2.2.1]heptan-2-one with N-C-N dinucleophiles

    Synthesis, pp. 1385-1391

  2. Synthesis and evaluation of adenosine antagonist activity of a series of [1,2,4]triazolo[1,5-c]quinazolines

    Chemical and Pharmaceutical Bulletin, Vol. 55, Núm. 3, pp. 372-375

  3. Synthesis of 4-substituted-1,2,3-triazole carbanucleoside analogues of ribavirin via click chemistry

    Organic and Biomolecular Chemistry, Vol. 5, Núm. 23, pp. 3805-3813

  4. Synthesis of cyclopenta[d]pyridazinediol precursors of carbanucleosides

    Synthesis, pp. 2621-2626

2006

  1. Regioselectivity in the formation of norbornene-fused pyrazoles: Preparation of 1-substituted derivatives of 4,5,6,7-tetrahydro-1H-4,7- methanoindazole

    Tetrahedron, Vol. 62, Núm. 14, pp. 3362-3369

  2. Synthesis of new 1′(N)-homocarbanucleosides based on 1-methylcyclopenta[c]pyrazole scaffold

    Synthesis, pp. 73-80

  3. Synthesis of purinyl and pyrimidinyl 1′(N)-homocarbanucleosides based on a 1-methylcyclopenta[c]pyrazole scaffold; part 2

    Synthesis, pp. 3967-3972

  4. The use of (-)-8-phenylisoneomenthol and (-)-8-phenylmenthol in the enantioselective synthesis of 3-functionalized 2-azabicyclo[2.2.1]heptane derivatives via aza-Diels-Alder reaction

    Tetrahedron, Vol. 62, Núm. 40, pp. 9475-9482

2005

  1. Synthesis of enantiopure cyclobutane amino acids and amino alcohols

    Tetrahedron Asymmetry, Vol. 16, Núm. 15, pp. 2593-2597

  2. Synthesis of purinyl homo-carbonucleoside derivatives of 2-benzylcyclopenta[c]pyrazol

    Synthesis, pp. 925-932