Fotoluminescenza:
Lakowicz, J. R. Principles of Fluorescence Spectroscopy; Plenum: New York, 1983
Diodi organici a emissione di luce (OLED):
Liu, S.-F.; Wu, Q.; Schmider, H. L.; Aziz, H.; Hu,N.-X.; Popovic ́, Z.; Wang, S. J. Am. Chem. Soc. 2000, 122, 3671-3678
Wang, S. Coord. Chem. Rev. 2001, 215, 79–98
Liu, Q.; Mudadu, M.S.; Schmider, H.; Thummel, R.; Tao, Y.; Wang, S. Organometallics 2002,
21, 4743-4749
Liu, Q.-D; Mudadu, M.S.; Schmider, H.; Thummel, R.; Tao, Y.; Wang, S. Adv. Funct. Mater. 2005, 15, 143-154
Trasferimento di protone nello stato eccitato (ESPT):
Herbich, J.; Hung, C.-Y.; Thummel, R. P.; Waluk, J. J. Am. Chem. Soc. 1996, 118, 3508-3518.
Wiosna G.; Petkova I.; Mudadu M. S.; Thummel R. P. Waluk J. Chemical Physics Letters, 2004, 400, 379–383
Wiosna-Salyga, G.; Dobkowski, J.; Mudadu, M. S.; Sazanovich, I.; Thummel, R. P.; Waluk, J. Chem. Phys. Lett. 2006, 423, 288-292
Petkova, I.; Mudadu, M.S.; Singh, A.; Thummel, R. P.; van Stokkum, I. H. M.; Buma, W. J.; Waluk, J. J. Phys. Chem. A, 2007, 111, 11400–11409
Synthesis:
• Sintesi di Fischer:
Sugasawa, S.; Terashima, M.; Kanaoka, Y. Pharm. Bull., 1956, 4, 16-19
Robinson, B. Chem. Rev. 1963, 63, 373-401
Pilgram K. H., Synth. Commun., 1985, 15, 697-706
Seki, K.-I.; Ohkura, K.; Terashima, M.; Kanaoka, Y. Chem. Pharm. Bull. 1988, 36, 940-944
Thummel, R. P.; Hegde, V. J . Org. Chem. 1989,54,1720-1725
Mudadu, M. S.; Singh, A.; Thummel, R.P. J. Org. Chem. 2006, 71, 7611-7617
• Reagente di Eaton:
Eaton, P. E.; Carlson, G. R.; Lee, J. T. J.Org. Chem., 1973, 38, 4071-4073
Zhao, D.; Hughes, D. L.; Bender, D. R.; DeMarco, A. M.; Reider, P. J. J. Org. Chem., 1991, 56,
3001-3006
Dixon, L. A. 2001; Phosphorus(V) Oxide–Methanesulfonic Acid; e-EROS Encyclopedia of Reagents for
Organic Synthesis
• Reazione di Bartoli:
Bartoli, G.; Palmieri G.; Bosco, M.; Dalpozzo, R.; Tetrahedron Lett.,1989, 30, 2129-2132
Bosco, M.; Dalpozzo, R.; Bartoli, G.; Palmieri G.; Petrini, M. J. Chem. Soc. Perkin Trans. 2, 1991, 657-663
Gribble, Gordon W. Indole ring synthesis: from natural products to drug discovery; Wiley: Chichester, West Sussex, 2016
• Scambio alogeno-litio:
Clayden, J. Organolithiums: Selectivity for Synthesis; Pergamon: Oxford, 2002
• Accoppiamento di Stille:
Kornblum, N. Org. Synth. 1955, 295–299, Collect. Vol. III
Grotta, H. M.; Riggle, C. J.; Bearse, A. E. J. Org. Chem. 1964, 29, 2474-2476
Neugebauer, F. A.; Hans Fischer, H. Chem. Ber. 1972, 105, 2686-2693
Åkermark, B.; Eberson, L.; Jonsson, E.; Pettersson, E. J. Org. Chem. 1975, 40, 1365–1367
Pieters, R. J.; Rebek, J. J. Recl. Trav. Chim. Pays-Bas 1993, 112, 330– 334
Schubert, U. S., Eschbaumer, C., Heller, M. Org. Lett., 2000, 2, 3373-3376
Gibson, V. C.; Spitzmesser, S. K.; White, A. J. P.; Williams, D. J. Dalton Trans. 2003, 2718–2727
Kürti, L., Czakó, B. Strategic Applications of Named Reactions in Organic Synthesis: background and detailed mechanisms; Elsevier Academic Press, 2005
Li, J. J.; Gribble, G. W. Palladium in Heterocyclic Chemistry, Volume 26, 2nd Edition, A Guide for the Synthetic Chemist; Elsevier Science, 2006
Mudadu, M. S.; Singh, A. N.; Thummel, R. P. J. Org. Chem. 2008, 73, 6513-6520
Liquidi ionici:
Wasserscheid, P.; Keim, W.; Angew. Chem. Int. Ed. 2000, 39, 3772-3789
Wasserscheid, P.; Welton, T. Ionic Liquids in Synthesis; Wiley-VCH, 2002
Calderon Morales, R.; Tambyrajah, V.; Jenkins, P. R.; Davies, D. L.; Abbott, A. P. Chem. Comm., 2004, 158-159
Chimica verde:
Dicks, A. P.; Hent, A. Green Chemistry Metrics, A Guide to Determining and Evaluating Process Greenness; Springer, 2015
