Dr Nancy Dervisi - PhD
Expanded-Ring and Backbone-Functionalised N-Heterocyclic Carbenes M. Iglesias, D. J. Beetstra, K. J. Cavell, A. Dervisi, I. A. Fallis, B. Kariuki, R. W. Harrington, W. Clegg, P. N. Horton, S. J. Coles, M. B. Hursthouse, Eur. J. Inorg. Chem., 2010, 14, 1604-1607. doi:10.1002/ejic.200901182
Expanded ring and functionalised expanded ring N-heterocyclic carbenes as ligands in catalysis A. Binobaid, M. Iglesias, D. J. Beetstra, B. Kariuki, A. Dervisi, I. A. Fallis, K. J. Cavell, Dalton Trans, 2009, 35, 7099-7112. doi:10.1039/b909834h
Novel expanded ring N-heterocyclic carbenes: Free carbenes, silver complexes, and structures A. Dervisi, I. A. Fallis, K. J. Cavell, M. Iglesias, D. Beetstra, A. Stasch, L.-L. Ooi; J. C. Knight, P. Horton, S. Coles, L. Male, M. Hursthouse, Organometallics, 2008, 27, 3279 - 3289. doi:10.1021/om800179t
The first examples of diazepan-ylidene carbenes and their late transition metal complexes Dervisi, A.; Fallis, I. A.; Cavell, K. J.; Iglesias, M.; Beetstra, D.; Stasch, A.; Horton, P.; Coles, S.; Hursthouse, M., Organometallics, 2007, 26, 4800 - 4809. doi:10.1021/om7004904
Chiral diphosphine ddppm-iridium complexes: effective asymmetric imine hydrogenations at ambient pressures A. Dervisi, C. Carcedo, L. Ooi, Adv. Synth. Catal., 2006, 175-183. doi:10.1002/adsc.200505276
A concise synthesis of a rigid isomannide-based diphosphine ligand and structural characterisation of an alkoxyphosphonium intermediate C. Carcedo, A. Dervisi, I. A. Fallis, L. Ooi and K. M. A. Malik, Chem. Commun., 2004, 1236-1237. doi:10.1039/b401301h
Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reaction A. Dervisi, D. Koursarou, L. Ooi, P. N. Horton, M. B. Hursthouse, Dalton Trans., 2006, 48, 5717-5724. doi:10.1039/b609607g
Synthesis of Ni(II), Pd(II) and Pt(II) complexes containing chiral phosphino-thiol and -thioether ligands A. Dervisi, R. L. Jenkins, K. M. A. Malik, M. B. Hursthouse, S. Coles, Dalton Trans., 2003, 6, 1133-1142. doi:10.1039/b209142a
