Structure-Activity Relationship of Clerodane Diterpenoids Acting as Antifeedant Agents von Enriz, R. D, Baldoni, H. A, Jauregui, E. A, Sosa, M. E, Tonn, C. E, Giordano, O. S

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An exploratory ab initio study of the full conformational space of N -acetyl- l -cysteine- N -methylamide von Zamora, M.A., Baldoni, H.A., Bombasaro, J.A., Mak, M.L., Perczel, A., Farkas, O., Enriz, R.D.

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Peptide models XXIX. cis – trans Isomerism of peptide bonds: ab initio study on small peptide model compound; the 3D-Ramachandran map of formylglycinamide von Baldoni, H.A., Zamarbide, G.N., Enriz, R.D., Jauregui, E.A., Farkas, Ö., Perczel, András, Salpietro, S.J., Csizmadia, I.G.

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Quantitative multidimensional conformational analysis of azadirachtin von Baldoni, H.A, Enriz, R.D, Csizmadia, I.G

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Exploratory molecular orbital calculations on the keto and enol forms of selected antifungals and those of side-chain substituted acetophenone model compounds von Rodrı́guez, A.M, Giannini, F.A, Baldoni, H.A, Suvire, F.D, Zacchino, S, Enriz, R.D, Csaszar, P, Csizmadia, I.G

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Conformational potential energy curves of acetophenone and α-substituted acetophenones von Rodrı́guez, A.M., Giannini, F.A., Baldoni, H.A., Santagata, L.N., Zamora, M.A., Zacchino, S., Sosa, C.P., Enriz, R.D., Csizmadia, I.G.

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Correlation of antifungal activity of selected α-substituted acetophenones with their keto–enol tautomerization energy von Rodrı&#x0301, guez, A.M., Giannini, F.A., Suvire, F.D., Baldoni, H.A., Furlán, R., Zacchino, S.A., Beke, G., Mátyus, P., Enriz, R.D., Csizmadia, I.G.

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