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Items by Caggiano, Lorenzo

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Number of items: 32.

2014

Ali Khan, M., Wood, P. J., Lamb-Guhren, N. M., Caggiano, L., Kociok-Köhn, G., Tosh, D. and Lewis, S. E., 2014. The enone motif of (+)-grandifloracin is not essential for 'anti-austerity' antiproliferative activity. Bioorganic & Medicinal Chemistry Letters, 24 (13), pp. 2815-2819.

2013

Ciupa, A., De Bank, P. A. and Caggiano, L., 2013. Multicellular aggregation of maltol-modified cells triggered by Fe3+ ions. Chemical Communications, 49 (86), pp. 10148-10150.

Ciupa, A., De Bank, P. A., Mahon, M. F., Wood, P. J. and Caggiano, L., 2013. Synthesis and antiproliferative activity of some 3-(pyrid-2-yl)-pyrazolines. MedChemComm, 4 (6), pp. 956-961.

Tunbridge, G. A., Baruchello, R. and Caggiano, L., 2013. Mild and efficient capture and functionalisation of CO2 using silver(I) oxide and application to 13C-labelled dialkyl carbonates. RSC Advances, 3 (14), pp. 4613-4621.

Tunbridge, G. A., Oram, J. and Caggiano, L., 2013. Design, synthesis and antiproliferative activity of indole analogues of indanocine. MedChemComm, 4 (11), pp. 1452-1456.

2012

Ciupa, A., Mahon, M., De Bank, P. and Caggiano, L., 2012. Simple pyrazoline and pyrazole “turn on” fluorescent sensors selective for Cd2+ and Zn2+ in MeCN. Organic and Biomolecular Chemistry, 10 (44), pp. 8753-8757.

2011

Ciupa, A., Griffiths, N. J., Light, S. K., Wood, P. J. and Caggiano, L., 2011. Design, synthesis and antiproliferative activity of urocanic-chalcone hybrid derivatives. MedChemComm, 2 (10), pp. 1011-1015.

Judd, K. E. and Caggiano, L., 2011. Bi(OTf)3-catalysed prenylation of electron-rich aryl ethers and phenols with isoprene: a direct route to prenylated derivatives. Organic and Biomolecular Chemistry, 9 (14), pp. 5201-5210.

2009

Judd, K. E., Mahon, M. F. and Caggiano, L., 2009. Efficient synthesis of tetrahydro-β-carbolin-1-one and dihydroisoquinolin-1-one derivatives as versatile intermediates. Synthesis, 2009 (16), pp. 2809-2817.

Nolasco, L., Perez Gonzalez, M., Caggiano, L. and Jackson, R. F. W., 2009. Application of Negishi Cross-Coupling to the Synthesis of the Cyclic Tripeptides OF4949-III and K-13. Journal of Organic Chemistry, 74 (21), pp. 8280-8289.

Drago, C., Walker, E. J., Caggiano, L. and Jackson, R. F. W., 2009. Enantioselective oxidation of an alkyl aryl sulfide : Synthesis of (S)-(-)-methyl p-Bromophenyl sulfoxide. Organic Syntheses, 86, pp. 121-129.

2008

Caggiano, L., Jackson, R. F. W., Meijer, A. J. H. M., Pickup, B. T. and Wilkinson, K. A., 2008. Ionisation of the zinc/iodine bond of alkylzinc iodides in dimethylformamide from theory and experiment. Chemistry - A European Journal, 14 (29), p. 8798.

Oswald, C. L., Carrillo-Marquez, T., Caggiano, L. and Jackson, R. F. W., 2008. Negishi cross-coupling reactions of alpha-amino acid-derived organozinc reagents and aromatic bromides. Tetrahedron, 64 (4), pp. 681-687.

Bartrum, H. E., Adams, H., Caggiano, L. and Jackson, R. F. W., 2008. Synthesis of β2-homophenylalanine derivatives by Negishi cross-coupling reactions. Tetrahedron, 64 (17), pp. 3701-3712.

Loghmani-Khouzani, H., Poorheravi, M. R., Sadeghi, M. M. M., Caggiano, L. and Jackson, R. F. W., 2008. α-Fluorination of β-ketosulfones by Selectfluor™ F–TEDA–BF4. Tetrahedron, 64 (30-31), pp. 7419-7425.

2007

Evans, L. A., Adams, H., Barber, C. G., Caggiano, L. and Jackson, R. F. W., 2007. Stereoselective synthesis of 2,3-difunctionalised thioesters using nucleophilic epoxidation of 1-arylthio-1-nitroalkenes. Organic and Biomolecular Chemistry, 5, pp. 31356-3163.

2006

Castoldi, D., Caggiano, L., Panigada, L., Sharon, O., Costa, A. M. and Gennari, C., 2006. A formal total synthesis of eleutherobin using the ring-closing metathesis (RCM) reaction of a densely functionalized diene as the key step: investigation of the unusual kinetically controlled RCM stereochemistry. Chemistry, 12, pp. 51-62.

Hinch, M., Jacques, O., Drago, C., Caggiano, L., Jackson, R. F. W., Dexter, C., Anson, M. S. and MacDonald, S. J. F., 2006. Effective asymmetric oxidation of enones and alkyl aryl sulfides. Journal of Molecular Catalysis A: Chemical, 251 (1-2), pp. 123-128.

Mohammadpoor-Baltork, I., Hill, M., Caggiano, L. and Jackson, R. F. W., 2006. Oxidative kinetic resolution of alky aryl sulfoxides. Synlett, 20, pp. 3540-3544.

Moreno, E., Nolasco, L. a., Caggiano, L. and Jackson, R. F. W., 2006. Synthesis of orthogonally protected biaryl amino acid derivatives. Organic and Biomolecular Chemistry, 4, pp. 3639-3647.

2005

Castoldi, D., Caggiano, L., Panigada, L., Sharon, O., Costa, A. M. and Gennari, C., 2005. A formal total synthesis of eleutherobin through an unprecedented kinetically controlled ring-closing-metathesis reaction of a densely functionalized diene. Angewandte Chemie-International Edition, 44, pp. 588-591.

Rilatt, I., Caggiano, L. and Jackson, R. F., 2005. Development and applications of amino ccid derived organometallics. Synlett, 18, pp. 2701-2719.

Carrillo-Marquez, T., Caggiano, L., Jackson, R. F. W., Graboswka, U., Rae, A. and Tozer, M. J., 2005. New routes to b-cycloalkylalanine derivatives using serine-derived organozinc reagents. Organic and Biomolecular Chemistry, 3, pp. 4117-4123.

Caggiano, L., 2005. Silicon-mediated transformations of functional groups (Book review). Applied Organometallic Chemistry, 19 (5), p. 699.

Castoldi, D., Caggiano, L., Bayon, P., Costa, A. M., Cappella, P., Sharon, O. and Gennari, C., 2005. Synthesis of novel, simplified, C-7 substituted eleutheside analogues with potent microtubule-stabilizing activity. Tetrahedron, 61, pp. 2123-2139.

Drago, C., Caggiano, L. and Jackson, R. F. W., 2005. Vanadium-catalyzed sulfur oxidation/kinetic resolution in the synthesis of enantiomerically pure alkyl aryl sulfoxides. Angewandte Chemie-International Edition, 44, pp. 7221-7223.

2003

Caggiano, L., Davies, J., Fox, D. J., Moody, D. C. and Warren, S., 2003. A novel silica catalysed stereoselective cyclic carbamate and carbonate rearrangement. Chemical Communications, 14, pp. 1650-1651.

Caggiano, L., Castoldi, D., Beumer, R., Bayon, P., Telser, J. and Gennari, C., 2003. Effects of allylic and homoallylic substituents on the ring closing metatheses reaction used to synthesise simplified eleuthesides. Tetrahedron Letters, 44, pp. 7913-7919.

Caggiano, L., Davies, J., Fox, D. J., Moody, D. C. and Warren, S., 2003. Stereoselective substituted pyrrolidine and cyclic ether synthesis by PhS migration. Chemical Communications, 14, pp. 1648-1649.

2002

Caggiano, L., Fox, D. J., House, D., Jones, Z. A., Kerr, F. and Warren, S., 2002. Asymmetric synthesis of tetrahydrofurans by competitive [1,2]-phenylsulfanyl (PhS) migrations under thermodynamic control. Journal of the Chemical Society - Perkin Transcriptions 1, 23, pp. 2634-2645.

Caggiano, L., Fox, D. J., House, D., Jones, Z. A., Kerr, F. and Warren, S., 2002. Asymmetric synthesis of tetrahydropyrans with competitive [1,2]-phenylsulfanyl (PhS) migrations. Journal of the Chemical Society - Perkin Transcriptions 1, 23, pp. 2646-2651.

Caggiano, L., Fox, D. J. and Warren, S., 2002. Silica gel catalysed generation of episulfonium ions: a mild method for the synthesis of heterocycles. Chemical Communications

This list was generated on Mon Sep 1 19:01:59 2014 IST.