Search Results - "Villalonga-Barber, C" :: K.UTB vyhledávací portál

Efficient microwave-assisted synthetic protocols and in silico behaviour prediction of per-substituted beta-cyclodextrins

by Martina, K., Cravotto, G., Caporaso, M., Rinaldi, L., Villalonga-Barber, C., Ermondi, G.
Published in Organic & biomolecular chemistry (07.09.2013)

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Efficient microwave-assisted synthetic protocols and in silico behaviour prediction of per-substituted β-cyclodextrinsElectronic supplementary information (ESI) available: Spectra 1H, 13C, 2D HMQC NMR, MS of all compounds. See DOI: 10.1039/c3ob40909k

by Martina, K, Cravotto, G, Caporaso, M, Rinaldi, L, Villalonga-Barber, C, Ermondi, G
Year of Publication 31.07.2013

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Engineered Chimeric Enzymes as Tools for Drug Discovery: Generating Reliable Bacterial Screens for the Detection, Discovery, and Assessment of Estrogen Receptor Modulators

by Skretas, Georgios, Meligova, Aggeliki K, Villalonga-Barber, Carolina, Mitsiou, Dimitra J, Alexis, Michael N, Micha-Screttas, Maria, Steele, Barry R, Screttas, Constantinos G, Wood, David W
Published in Journal of the American Chemical Society (11.07.2007)

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Studies towards a stereocontrolled synthesis of the tricarboxylate core of the zaragozic acids–squalestatins by a cycloaddition–rearrangement strategy

by Hodgson, David M., Villalonga-Barber, Carol
Published in Tetrahedron letters (15.07.2000)

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Selective catalytic carbanionic ethylation of methylphenols: influence of catalyst and substitution pattern

by Steele, Barry R., Villalonga-Barber, Carolina, Micha-Screttas, Maria, Screttas, Constantinos G.
Published in Tetrahedron letters (27.03.2006)

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Synthesis and Diels-Alder reactivity of chiral 2-(alk-1-enyl)-1,3,2-diazaphospholidine 2-oxides

by Wyatt, Peter B., Villalonga-Barber, Carolina, Motevalli, Majid
Published in Tetrahedron letters (1999)

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Selectivity in the cycloadditions of carbonyl ylides with glyoxylates: an approach to the zaragozic acids-squalestatins

by Hodgson, DM, Bailey, JM, Villalonga-Barber, C, Drew, MGB, Harrison, T
Published in Perkin 1 : an international journal of organic and bio-organic chemistry (01.01.2000)

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Efficient microwave-assisted synthetic protocols and in silico behaviour prediction of per-substituted beta-cyclodextrins

Efficient microwave-assisted synthetic protocols and in silico behaviour prediction of per-substituted β-cyclodextrinsElectronic supplementary information (ESI) available: Spectra 1H, 13C, 2D HMQC NMR, MS of all compounds. See DOI: 10.1039/c3ob40909k

Engineered Chimeric Enzymes as Tools for Drug Discovery: Generating Reliable Bacterial Screens for the Detection, Discovery, and Assessment of Estrogen Receptor Modulators

Studies towards a stereocontrolled synthesis of the tricarboxylate core of the zaragozic acids–squalestatins by a cycloaddition–rearrangement strategy

Selective catalytic carbanionic ethylation of methylphenols: influence of catalyst and substitution pattern

Synthesis and Diels-Alder reactivity of chiral 2-(alk-1-enyl)-1,3,2-diazaphospholidine 2-oxides

Selectivity in the cycloadditions of carbonyl ylides with glyoxylates: an approach to the zaragozic acids-squalestatins

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