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N-Hydroxyphthalimid (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "N-Hydroxyphthalimid" in German language version.

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18doi.org
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5google.com
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2tcichemicals.com
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1sigmaaldrich.com
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doi.org

  • L. Bauer, S.V. Miarka: The Chemistry of N-Hydroxyphthalimide. In: J. Am. Chem. Soc. Band 79, Nr. 8, 1957, S. 1983–1985, doi:10.1021/ja01565a061.
  • C. Gambarotti, C. Punta, F. Recupero, M. Zlotorzynska, G. Sammis: N-Hydrophthalimide. In: e-EROS Encyclopedia of Reagents for Organic Synthesis. 2013, doi:10.1002/047084289X.rn00598.pub2.
  • F. Recupero, C. Punta: Free Radical Functionalization of Organic Compounds Catalyzed by N-Hydroxyphthalimide. In: Chem. Rev. Band 107, Nr. 9, 2007, S. 3800–3842, doi:10.1021/cr040170k.
  • L. Melone, C. Punta: Metal-free aerobic oxidations mediated by N-hydroxyphthalimide. A concise review. In: Beilstein J. Org. Chem. Band 9, 2013, S. 1296–1310, doi:10.3762/bjoc.9.146.
  • L. Cohn: Phthalylhydroxylamin: Ueberführung der Phthalsäure in Salicylsäure. In: Justus Liebigs Ann. Chem. Band 205, Nr. 3, 1880, S. 295–314, doi:10.1002/jlac.18802050304.
  • H. Gross, I. Keitel: Zur Darstellung von N-Hydroxyphthalimid und N-Hydroxysuccinimid. In: J. prakt. Chem. Band 311, Nr. 4, 1969, S. 692–693, doi:10.1002/prac.19693110424.
  • K. Sugamoto, Y. Matsushita, Y. Kameda, M. Suzuki, T. Matsui: Microwave-assisted synthesis of N-hydroxyphthalimide. In: Synth. Commun. Band 35, Nr. 1, 2005, S. 67–70, doi:10.1081/SCC-200046498.
  • H. Reichelt, C.A. Faunce, H.H. Paradies: Elusive forms and structures of N-hydroxyphthalimide: the colorless and yellow crystal forms of N-hydroxyphthalimide. In: J. Phys. Chem. Band 111, Nr. 13, 2007, S. 2587–2601, doi:10.1021/jp068599y.
  • D.E. Ames, T.F. Grey: N-Hydroxy-imides. Part II. Derivatives of homophthalic and phthalic acid. In: J. Chem. Soc. 1955, S. 3518–3521, doi:10.1039/JR9550003518.
  • O.L. Brady, L.C. Baker, R.F. Goldstein, S. Harris: LXVIII. – The isomerism of the oximes. Part XXXIII. The oximes of opianic acid and of phthalic anhydride. In: J. Chem. Soc. 1928, S. 529–539, doi:10.1039/JR9280000529.
  • C.D. Hurd, C.M. Buess, L. Bauer: Succino- and phthalo-hydroxamic acids. In: J. Org. Chem. Band 19, Nr. 7, 1954, S. 1140–1149, doi:10.1021/jo01372a021.
  • G.H.L. Nefkens, G.I. Tesser: A novel activated ester in peptide synthesis. In: J. Am. Chem. Soc. Band 83, Nr. 5, 1961, S. 1263–1263, doi:10.1021/ja01466a068.
  • S. Coseri: Phthalimide‐N‐oxyl (PINO) Radical, a Powerful Catalytic Agent: Its Generation and Versatility Towards Various Organic Substrates. In: Catal. Rev. Sci. Eng. Band 51, Nr. 2, 2009, S. 218–292, doi:10.1080/01614940902743841.
  • Y. Ishii, K. Nakayama, M. Takeno, S. Sakaguchi, T. Iwahama, Y. Nishiyama: Novel Catalysis by N-Hydroxyphthalimide in the Oxidation of Organic Substrates by Molecular Oxygen. In: J. Org. Chem. Band 60, Nr. 13, 1995, S. 3934–3935, doi:10.1021/jo00118a002.
  • B.B. Wentzel, M.P.J. Donners, P.L. Alsters, M.C. Feiters, R.J.M. Nolte: N-Hydroxyphthalimide/cobalt(II) catalyzed low temperature benzylic oxidation using molecular oxygen. In: Tetrahedron. Band 56, 2000, S. 7797–7803, doi:10.1016/S0040-4020(00)00679-7.
  • F. Minisci, C. Punta, F. Recupero, F. Fontana, G.F. Pedulli: Aerobic Oxidation of N-Alkylamides Catalyzed by N-Hydroxyphthalimide under Mild Conditions. Polar and Enthalpic Effects. In: J. Org. Chem. Band 67, Nr. 8, 2002, S. 2671–2676, doi:10.1021/jo16398e.
  • O. Fukuda, S. Sakaguchi, Y. Ishii: A new strategy for catalytic Baeyer-Villiger oxidation of KA-oil with molecular oxygen using N-hydroxyphthalimide. In: Tetrahedron Lett. Band 42, Nr. 20, 2001, S. 3479–3481, doi:10.1016/S0040-4039(01)00469-5.
  • S. Sakaguchi, Y. Nishiwaki, T. Kitamura, Y. Ishii: Efficient catalytic alkane nitration with NO2 under air assisted by N-hydroxyphthalmide. In: Angew. Chem., Int. Edit. Band 40, Nr. 1, 2001, S. 222–224, doi:10.1002/1521-3773(20010105)40:1<222::AID-ANIE222>3.0.CO;2-W.

google.com

  • Patent EP1085013: Verfahren zur Herstellung cyclischer N-Hydroxy-dicarboximide. Angemeldet am 31. August 2000, veröffentlicht am 21. März 2001, Anmelder: Consortium für elektrochemische Industrie GmbH, Erfinder: E. Fritz-Langhals.‌
  • Patent EP0919867B1: Chemisch verstärkter Resist für die Elektronenstrahllithografie. Angemeldet am 17. November 1998, veröffentlicht am 21. Mai 2003, Anmelder: Infineon Technologies AG, Erfinder: K. Elian, E. Günther, R. Leuschner.‌
  • Patent WO1995025090: Cyclic N-alkenyloxyimides and a method for the preparation of cyclic N-alkenyloxyimides, the corresponding cyclic N-alkoxyimides and O-alkoxyamines. Angemeldet am 14. März 1995, veröffentlicht am 21. September 1995, Anmelder: DSM N.V., Erfinder: D.M.C. Callant, A.M.C.F. Castelijns, J.G. De Vries.‌
  • Patent EP0664479A1: Method of processing silver halide photographic lightsensitive material. Angemeldet am 6. Dezember 1994, veröffentlicht am 26. Juli 1995, Anmelder: Konica Corp., Erfinder: W. Ishikawa, T. Sampei.‌
  • Patent US5332637: Electrostatographic dry toner and developer compositions with hydroxyphthalimide. Angemeldet am 31. August 1993, veröffentlicht am 26. Juli 1994, Anmelder: Eastman Kodak Co., Erfinder: J.C. Wilson, S.M. Bonser, H.W. Osterhoudt.‌

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