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UNIVERSITY OF PERUGIA

Dpt. Pharm. Sciences

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Curriculum Vitae
updated May 2014
CV_Santi_May2014.pdf
Documento Adobe Acrobat 1.0 MB

in evidence

Published May 2014
Published May 2014
RSC Advances at Eurasia 2012
RSC Advances at Eurasia 2012

2017

  1. Sancineto, L., Mangiavacchi, F,,Tidei, C., Bagnoli, L., Marini, F., Scianowski, J., Gioiello, A. and Santi, C. Selenium catalyzed oxacyclization of alkenoic acids and alkenols. (2017), Asian J. Org. Chem. Accepted Author Manuscript doi
  2. Mazzeo, G., Longhi, G., Abbate, S., Palomba, M., Bagnoli, L., Marini, F., Santi, C., Han, J., Soloshonok, V.A., Di Crescenzo, E.; Ruzziconi, R. Solvent-free, uncatalyzed asymmetric “ene” reactions of N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimines: a general approach to enantiomerically pure α-(trifluoromethyl)tryptamines

    (2017) Org. Biomol. Chem., Advance Article doi   

  3. Casula, A., Llopis-Lorente, A., Garau, A., Isaia, F., Kubicki, M., Lippolis, V., Sancenón, F., Martínez-Máñez, R., Owczarzak, A., Santi, C.,  Scorciapino M.A., Caltagirone, C A New class of silica-supported chromo-fluorogenic chemosensors for anion recognition based on a selenourea scaffold

    (2017) Chem. Commun.,53, 3729-3732 doi

  4. Perin, G; Barcellos, AM; Luz, EQ ; Borges, EL; Jacob, RG; Lenardao, EJ; Sancineto, L; Santi, C  Green Hydroselenation of Aryl Alkynes: Divinyl Selenides as a Precursor of Resveratrol

    (2017) Molecules 22 (2), 327 doi

  5. S. Fiorito, F. Epifano, F. Preziuso, V.A. Taddeo, C. Santi, S. Genovese New insights into the seleniranium ion promoted cyclization of prenyl and propenylbenzene aryl ethers Tetrahedron Letters 58 (2017) 371–374 doi
  6. C Tomassini, F. Di Sarra, B. Monti, L. Sancineto, L. Bagnoli, F Marini, C. Santi Kinetic resolution of 2-carbomethoxy-3-alkenols through a stereoselective cyclofunctionalization promoted by an enantiomerically pure electrophilic selenium reagent Arkivoc (2017) In press doi
  7. A. M. Barcellos, L. Abenante, M. T. Sarro, I. Di Leo, E. J. Lenardao, G. Perin, C. Santi New Prospective for Redox Modulation mediated by Organoselenium and Organotellurium Compounds Current Organic Chemistry (2017), 20, doi