Diseño, interacción y síntesis de compuestos biológicamente activos - Design, interaction and synthesis of bioactive compounds.
DISCOBAC


Centre National de la Recherche Scientifique
París, FranciaPublications in collaboration with researchers from Centre National de la Recherche Scientifique (12)
2017
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Structure-activity relationship study of vitamin D analogs with oxolane group in their side chain
European Journal of Medicinal Chemistry, Vol. 134, pp. 86-96
2016
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Synthesis and biological evaluation of benzochromenopyrimidinones as cholinesterase inhibitors and potent antioxidant, non-hepatotoxic agents for Alzheimer's disease
Molecules, Vol. 21, Núm. 5
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Synthesis, regioselectivity, and DFT analysis of new antioxidant pyrazolo[4,3-c]quinoline-3,4-diones
Monatshefte fur Chemie, Vol. 147, Núm. 6, pp. 1069-1079
2015
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Stimulating excursions into organolead chemistry: modular domino sequences triggered by oxidative cleavage
Tetrahedron Asymmetry, Vol. 26, Núm. 18-19, pp. 981-1035
2013
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Increasing the dimensionality of modular domino reactions triggered by oxidative cleavage: A two-step protocol towards a variety of stereodefined complex oxygen heterocycles
European Journal of Organic Chemistry, pp. 2401-2413
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Modular construction of topologically complex polycyclic acetals by tether-controlled domino reactions
European Journal of Organic Chemistry, pp. 2389-2400
2012
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Diverging pathways to topologically complex polycyclic bis-acetals and their ring system interchange
Organic Letters, Vol. 14, Núm. 6, pp. 1628-1631
2010
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Efficient construction of highly substituted and stereodefined cis-fused lactones
European Journal of Organic Chemistry, pp. 4851-4860
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Synthetic studies directed towards various homologues of natural Sesquiterpene-Coumarin ethers: The Domino approach
European Journal of Organic Chemistry, pp. 1483-1493
2009
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Competing domino processes: Path-discriminating ability of epoxide stereochemistry at the angular position
Organic Letters, Vol. 11, Núm. 16, pp. 3610-3613
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Microwave-assisted competing domino processes in the octaline diol series
European Journal of Organic Chemistry, pp. 2687-2694
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Natural and unnatural A-seco terpenes from pulegone: Synthesis of galbanic acid and marneral revisited
European Journal of Organic Chemistry, pp. 6386-6392