RICERCA ITALIANA     

Programmi di ricerca simili:

• 1 - Ingegnerizzazione e sviluppo di catalizzatori molecolari o nanostrutturati e strategie sintetiche sostenibili (alta selettività e resa) per la produzione di sistemi molecolari complessi da unità semplici ed eco-compatibili.
• 2 - Sintesi e reattività/attività di sistemi insaturi funzionalizzati. Parte II.
• 3 - Attivazione ossidativa catalitica e fotocatalitica per la sintesi organica
• 4 - ETEROCICLI NON AROMATICI IN PROCESSI STEREOCONTROLLATI
• 5 - Attivazione ossidativa di molecole organiche attraverso nuovi processi catalitici e fotocatalitici
• 6 - Metodologie e strategie sintetiche orientate alla creazione di diversità molecolare per la preparazione di molecole biologicamente attive
• 7 - Sintesi diretta di H2O2 e suo uso integrato in sistemi nanoconfinati
• 8 - Processi chimici realizzati in presenza di campo elettromagnetico per una Chimica Sostenibile
• 9 - ELETTROCATALISI ED ELETTROSINTESI
• 10 - Catalizzatori innovativi a base di metalli di transizione per sintesi mirate chemo- e stereo-selettive

Classificazione scientifico-disciplinare

• Area scientifico disciplinare: Scienze chimiche
  • CHIMICA ORGANICA
  • CHIMICA E BIOTECNOLOGIA DELLE FERMENTAZIONI

Classificazione brevettuale

• CHEMISTRY; METALLURGY
  • ORGANIC CHEMISTRY (such compounds as the oxides, sulfides, or oxysulfides of carbon, cyanogen, phosgene, hydrocyanic acid or salts thereof C01; products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds C01B33/44; macromolecular compounds C08; dyes C09; fermentation products C12; fermentation or enzyme-using processes to synthesise a desired chemical compound or composition or to separate optical isomers from a racemic mixture C12P; production of organic compounds by electrolysis or electrophoresis C25B3/00, C25B7/00)
    • GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR (preparation of carboxylic acid esters by telomerisation C07C67/47; telomerisation C08F)

Classificazione geografica

• Regione: Toscana

Bibliografia

[1]Aversa, M.C. et al., J.Org.Chem.2002,67,6925
[2]Aversa, et al., a) J.Org.Chem.1997, 62,4376 b) Tetrahedron: Asymmetry 2001,12,2901
[3]Aversa, M.C. et al., a) Tetrahedron:Asymmetry 1997,8,2989 b) Ibid 1999,10,3919 c) Arkivoc 2004,79
[4]Aversa, M.C.; et al., Synthesis 2003, 2241
[5]Aversa, M.C.; et al., J.Org.Chem. 2001,66,4845
[6]Aversa, M.C.; et al., Ibid 2005,70,1986
[7]Choudary, B.M.; et al., Green Chem. 1999,1,289
[8](a)Knapp, S.; et al., Org.Lett. 1999, 1,611.(b) Driguez, H. Chembiochem 2001, 2, 311.
[9](a)Kadaba, P. K.; et al., Adv. Het. Chem. 1984, 37, 217 (b) F. Clerici, Advances in Heterocyclic Chemistry, A. R. Katritzky ed., Pergamon Press, vol. 83, 72-116, 2002
[10]Gelmi, M. L. et al., Org. Prep. Proc. Int. 2003,35,141
[11](a) Dowle, M. D.; et al., Chem.Soc. Rev.1979,8,171. (b) Gelmi, M. L. et al.: Tetrahedron 2001,57,6429; J.Org. Chem. 2001,66,4941. (c) Zhang, D et al., Ibid 1998,63,755
[12]DeClercq et al.: Biochem. Pharmacol. 1983,3583
[13]Lupetti et al. Trends in Mol. Med. 2003,9,269
[14]Fazio, A.; et al., Tetrahedron 2000, 56
[15]Palomo, C.; et al.,J.Org.Chem. 2001,66
[16]Davis, F.A.; et al.,J.Org.Chem. 2000,65,7663
[17] Dalla Croce, P.; et al.,. (a) Heterocycles, 2000, 52,1337; (b)Tetrahedron: Asymmetry, 2000, 11, 2635; c) Heterocycles, 2003,61,563
[18](a)Vogt, P. F et al., Tetrahedron 1998,54,1317(b) Adam, W.; et al.,Chem. Rev. 2003,103, 4131.
[19]Boger, L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic Press: San Diego, 1987
[20]Keck, G. E.; et al.,Tetrahedron 1981,37,4016
[21] Caramella, P. et al., (a) Tetrahedron Lett. 1996,37,1909; (b) Tetrahedron 1999,55,10497
[22](a) Caramella, P.; Grünanger, P. 1,3-Dipolar Cycloaddition Chemistry, Padwa, A. Eds.; John Wiley and Sons, Inc.: New York, 1984, pp. 291-392. Caramella, P. et al., (a) Tetrahedron Lett. 2001,42,731; (b) Ibid 2001, 42, 5077; (c) J. Am. Chem. Soc. 2002, 24,1130; (d) J.Org.Chem. 2003,68,6035; (e) Tetrahedron Lett. 2002, 43, 8785; (g) J. Am. Chem. Soc. 2003, 125, 15420
[23]Caramella, P. et al., Tetrahedron 1997,53,1787
[24]Caramella, P. et al., Tetrahedron Lett. 1999, 40,797
[25]Crimmins, M. T. et al., Tetrahedron 1998, 54,9229
[26]Caramella, P.; et al., Eur. J.Org.Chem., 2000, 261
[27](a) Streith, J.; et al., Synthesis 1994, 1107. (b) Streith, J.; et al., Ibid 1996, 189
[28]Caramella, P.; et al., Tetrahedron 2004, 60, 3643
[29]Singlet Oxygen; Frimer, A. A. Ed.; CRC Press: Boca Raton (Fl), 1985
[30] Iesce, M.R.; et al.,Curr. Org. Chem. 2005, 9, 109 and references cited therein
[31] Iesce, M.R.; et al., a) Synthesis, 1994, 944; b) Synlett, 1995, 1161; c) Synthesis,1995, 439; d) Synthesis, 1997, 657; e) Synthesis, 1998,333; f) Synlett, 1999,417
[32] Iesce, M. R.; et al., a) J.Org.Chem. 1996,61,8677; b) J.Org.Chem. 1998,63,9528; c) J.Org.Chem. 2001,66,4732
[33] Iesce, M. R.; et al., a) J.C.S., Chem. Commun., 1989,1608; b) J.C.S., Perkin Trans. 1, 1994,3295; c) J.Org.Chem., 1995,60,5324
[34]a) Suhadolnik, R. J. Nucleoside Antibiotics; Wiley-Interscience: New York, 1970; b) Shaban, M. A. E. and Nasr, A. Z. InAdvances in Heterocyclic Chemistry; Katritzky, A. R., Ed.; Academic Press: London, 1997, Vol. 68, p. 385; c) Danishefsky, S. J.; et al., J. Am. Chem. Soc., 1985, 107, 1285; d) Olsen, A. G.; et al., J. Chem. Soc., Perkin Trans. 1,2001, 900 e) Sollogoub, M.; et al.,T. Tetrahedron Lett., 2002, 43, 3121.
[35] A. Brandi, et al.; In “Current Trends in Organic Synthesis” eds. C. Scolastico, F. Nicotra; Kluwer Academic/Plenum: New York, 1999; pp 213.
[36]A. Brandi, et al a) J.Org.Chem. 1995, 60, 6806. b) Synlett 1996, 761; c) J. Carbohydr. Chem. 2000, 19, 585; d) Org.Lett. 2001, 3, 1367 e) Tetrahedron Asymmetry 1996, 7, 1659; f) Eur. J.Org.Chem. 2002, 1941
[37]A. Brandi, et al a)Tetrahedron Lett. 1997, 38, 8097; b) J.Org.Chem. 1998, 63, 7311. c) Synlett 1998, 1444;d) Eur. J.Org.Chem. 1999, 1319; e) Org.Lett. 2003, 5, 1475.
[38]a) S.K. Das, Synlett 2004, 915. b) A. Loupy, C. R. Chimie 2004,7,103. c)B.L.Hayes, Aldrichimica Acta 2004, 37, 66.
[39](a) Caramella, P. et al., Tetrahedron 2000, 56, 4299 (b) Corsaro, A.; et al., Synthesis 2000, 1469. (c) Chiacchio, U.; et al., (i) Tetrahedron: Asymm. 2000, 2045 (ii) Tetrahedron 2001, 57, 3425 (iii) Eur.J.Org. Chem. 2002,1206 (iv)J. Med. Chem. 2003,46,3696 (v) Tetrahedron Lett. 2001,42, 1777(vi) Eur.J.Org.Chem. 2001,1893(vii)J.Org.Chem. 1999, 64, 28 (viii) J.Org.Chem. 1999, 64, 9321
[40](a)Santana, L.; et al., Eur. J. Med. Chem. 2002, 37, 755(b) Santana, L.; et al., Synthesis 2001,10,1532
[41](a) Schneller, S. W. Current Topics in Med. Chem. 2002,2,1087
[42]Bernet, B.; Vasella, A. Helv. Chim. Acta 1979, 62, 1990
[43](a)Chiacchio, U.; et al., Bioorg. Med. Chem. 2004, 12,3903(b) Saita, M.G.; et al., Nucleosides, Nucleotides Nucleic Acids 2003,22739(c) Chiacchio, U.; et al., T. Tetrahedron 2003, 59, 4733. (d) Chiacchio, U.; et al., Tetrahedron: Asymm. 2003,14,2717
[44](a) Wyatt, P. G.; et al., Nucleosides Nucleotides 1995, 14, 2039. (b) Katagiri, N.; et al., J. Chem. Soc. Perkin Trans. 1 1992, 589. (d) Shaw, G.; Warrener, R. J. Chem. Soc. 1958, 153
[45](a) Jenny, T.; et al., Helv. Chim. Acta 1992,75,1944. (b)Jenny, T.; et al., Nucleosides Nucleotides 1992,11,1257
[46](a)Marquez, V.; et al., J.Org.Chem. 1988,53,5709(b) Tseng,C.; Marquez, V. Tetrahedron Lett. 1985, 26, 3669.
[47]Jeong, L.S.; Jin, D. Z.; Kim, H. O.; Shin, D. H.; Moon, H. R.; Gunaga, P.; Chun, M. W.; Kim, Y.-C.; Melman, N.; Gao,Z.-G.;Jacobson, K. A. J. Med. Chem. 2003, 46, 3775
[48]Zhang, X.; Qing, F.-L. J.Org.Chem. 2002,67,1016
[49]Naka, T.; Minakawa, N.; Abe, H.; Kaga, D.; Matsuda, A. J. Am. Chem. Soc. 2000, 122,7233
[50]Kambampati, R.; Lauhon, C. T. Biochemistry 2003,42,1109
[51]Haraguchi, K.; Takahashi, H.; Shiina, N.; Horii, C.; Yoshimura, Y.; Nishikawa, A.; Sasakura, E.; Nakamura, K.T.; Tanaka, H.J.Org. Chem. 2002,67,5919
[52]Bluemling, G. R.; Bressette, A. R. 225th ACS National Meeting, New Orleans, LA, USA, March 23-27, 2003
[53]Matsuda, H. Kagaku to Kogyo 2001,54,1072
[54]Young, R. J. Drug Discovery Today 1996,1,123
[55]Yokoyama, M. Synthesis, 2000,12,1637
[56]Foti, F.; et al., Synlett 2005,125
[57].Cordaro, M.; et al. Synlett 2003, 1710
[58]Grassi, G.; Foti, F.; Risitano, F.; Zona, D. Tetrahedron Lett. 2005, 46, 1061-1062.
[59] a) Pollini, G. P.; et al., Synthesis 1987, 857 b) Kotyatkina, A. I. Russ. Chem. Rev. 2001,70,641and references cited therein
[60]Mukaiyama, T.; Hoshino T.; J. Am. Chem. Soc.1960,82,5339
[61]V.Vigalok, et al., Khim. Geterotsikl. Soedin. 1969, (1), 175
[62] Duranleau, R.G.; et al., U.S.Patent 4089867 (1978)
[63]Shimizu, T.; et al., Bull. Chem. Soc. Jpn.1984, 57, 2531
[64] Kaji, E.; et al., Chem. Pharm. Bull., 1978,26,3254
[65]Shimizu, T.; et al., Bull.Chem. Soc. Jpn.1986,59,2827
[66]Bachmann G.B.; Strom, L.E. J.Org.Chem. 1963,28,1150
[67]Basel Y.; Hassner, A. Synthesis 1997,309
[68] Tsushima, S. et al., Jp Patent 24902 (1968); Chem .Abs. 1969,70,87344
[69]Leslie-Smith, M.G.; et al.,Tetrahedron. Lett. 1994,35,9251
[70]McKillop A.; Kobylecki, R.J. Tetrahedron,1974,30,1365
[71]Rahman, A.; et al., J. Chem. Soc. Pak. 1983,5,243
[72]Rahman, A.; et al., J. Sci. Res. 1978,30,91
[73] a) Grund, H.; Jaeger, V. Liebigs Ann.Chem.1980,80 b) Shimizu, T. et al.,Bull.Chem Soc. Jpn. 1986,59,2827
[74]Kwiatowsky S.; Langwald, M. Monatsh. Chem. 1986,117,1091
[75]Nelson, S. D.; et al., J.Org.Chem. 1972,37,2686
[76]Kaji, E.; et al., Chem.Pharm. Bull. 1978,26,3254
[77]S.Kwiatowsky et al., Monatsh. Chem. 1986,117,1091
[78] Beck, W.; et al., a) Angew. Chem. Int. Ed. 1971,10,66 b) Ber. 1974,107,1371 c) J. Organomet. Chem. 1986,314,C55-C58
[79]Faita, G.; et al., Eur. J.Org.Chem. 2002, 1175
[80](a)Gandolfi, R.; et al., Tetrahedron:Asymmetry 2002,13,2345 (b)Molinari, F.; et al., Ibid 2004,15,1945 (c) Converti, A et al., Enzyme Microb. Technol.,2005,36, 432

Parole Chiave

CICLOADDIZIONE [3+2]; 1,3-DIPOLI; RIDOTTO IMPATTO AMBIENTALE; STEREOSELETTIVITA'; REAZIONI SU FASE SOLIDA; AMMINOACIDI, ZUCCHERI E NUCLEOSIDI MODIFICATI; CICLOADDIZIONE [4+2]; OSSIGENO SINGOLETTO