FRANCO
FERNANDEZ GONZALEZ
Researcher in the period 1976-2018
MARIA OLGA
CAAMAÑO SANTOS
Researcher in the period 1991-2021
Publications by the researcher in collaboration with MARIA OLGA CAAMAÑO SANTOS (60)
2013
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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
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A 'click chemistry' approach to the straightforward synthesis of new 4-aryl-1,2,3-triazolocarbanucleosides
Arkivoc, Vol. 2010, Núm. 3, pp. 152-168
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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
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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
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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
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Synthesis and biological evaluation of 6-substituted purinylcarbanucleosides with a cyclopenta[b]thiophene pseudosugar
Synthesis, pp. 2766-2772
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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
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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
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Synthesis and antiviral activities of novel purinyl- and pyrimidinyl-carbanucleosides derived from indan
Synthesis, pp. 1845-1852
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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
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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
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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
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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
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Synthesis of cyclopenta[d]pyridazinediol precursors of carbanucleosides
Synthesis, pp. 2621-2626
2006
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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
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Synthesis of new 1′(N)-homocarbanucleosides based on 1-methylcyclopenta[c]pyrazole scaffold
Synthesis, pp. 73-80
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Synthesis of purinyl and pyrimidinyl 1′(N)-homocarbanucleosides based on a 1-methylcyclopenta[c]pyrazole scaffold; part 2
Synthesis, pp. 3967-3972
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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
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Synthesis of enantiopure cyclobutane amino acids and amino alcohols
Tetrahedron Asymmetry, Vol. 16, Núm. 15, pp. 2593-2597
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Synthesis of purinyl homo-carbonucleoside derivatives of 2-benzylcyclopenta[c]pyrazol
Synthesis, pp. 925-932