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1-Hydroxybenzotriazol (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "1-Hydroxybenzotriazol" in German language version.

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9doi.org
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2europa.eu
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1reach-clp-biozid-helpdesk.de
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doi.org

  • Bosch, R.; Jung, G.; Winter, W.: Benzotriazole 1-oxide and 1-hydroxybenzotriazole, C6H5N3O: structures of both tautomeric forms in Acta Crystallogr. Sect. C 39 (1983) 1089–1092, doi:10.1107/S0108270183007490.
  • Pfister-Guillouzo, G.; Gracian, F.; Paez, J.A.; Gomez, C.G.; Elguero, J.: Study of 1-hydroxybenzotriazole/benzotriazole N-oxide tautomerism in gas phase by photoelectron spectroscopy in Spectrochim. Acta A51 (1995) 1801–1807, doi:10.1016/0584-8539(95)01441-V.
  • Boyle, F.T.; Jones, R.A.Y.: Azole N-oxides. Part I. The tautomerism of benzotriazole 1-oxide and its 4- and 6-nitro-derivatives with the corresponding 1-hydroxybenzotriazoles in J. Chem. Soc. Perkin Trans. 2, 1973, 160–164, doi:10.1039/P29730000160.
  • Fu, Jie; Yang, Ying; Zhang, Xue-Wei; Mao, Wen-Jun; Zhang, Zhi-Ming; Zhu, Hai-Liang: Discovery of 1H-benzo[d][1,2,3]triazol-1-yl 3,4,5-trimethoxybenzoate as a potential antiproliferative agent by inhibiting histone deacetylase. In: Bioorganic & Medicinal Chemistry 18 (2010) 8457–8462, doi:10.1016/j.bmc.2010.10.049.
  • Fruchier, A.; Elguero; J.; Hagarty, A.F.; McGarthy, D.G.: NMR studies in the heterocyclic series. XX—a carbon-13 NMR study of the structures of N-hydroxybenzotriazole and its acylated derivatives in Org. Magn. Reson. 13 (1980) 339–342, doi:10.1002/mrc.1270130508.
  • Schilf, W.; Stefaniak, L.; Witanowski, M.; Webb, G.A.: 15N NMR studies of the tautomeric equilibrium of some 1-hydroxybenzotriazoles in Magn. Reson. Chem. 23 (1985) 181–184, doi:10.1002/mrc.1260230310.
  • Wehrstedt, K.D.; Wandrey, P.A.; Heitkamp, D.: Explosive properties of 1-hydroxybenzotriazoles in J. Hazard. Mat. A126 (2005) 1–7, doi:10.1016/j.jhazmat.2005.05.044.
  • Wolfgang König, Rolf Geiger: Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1-Hydroxy-benzotriazolen. In: Chemische Berichte. 103, 1970, S. 788, doi:10.1002/cber.19701030319.
  • R. Subirós-Funosas, R. Prohens, R. Barbas, A. El-Faham, F. Albericio: Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. In: Chemistry. Band 15, Nummer 37, September 2009, S. 9394–9403, doi:10.1002/chem.200900614. PMID 19575348.

europa.eu

echa.europa.eu

nih.gov

ncbi.nlm.nih.gov

  • R. Subirós-Funosas, R. Prohens, R. Barbas, A. El-Faham, F. Albericio: Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. In: Chemistry. Band 15, Nummer 37, September 2009, S. 9394–9403, doi:10.1002/chem.200900614. PMID 19575348.

reach-clp-biozid-helpdesk.de

sigmaaldrich.com

unece.org