Curtius rearrangement (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Curtius rearrangement" in English language version.

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  • Curtius, Th. (1890). "Ueber Stickstoffwasserstoffsäure (Azoimid) N3H" [On hydrazoic acid (azoimide) N3H]. Berichte der Deutschen Chemischen Gesellschaft zu Berlin. 23 (2): 3023–3033. doi:10.1002/cber.189002302232.

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  • Curtius, Th. (1890). "Ueber Stickstoffwasserstoffsäure (Azoimid) N3H" [On hydrazoic acid (azoimide) N3H]. Berichte der Deutschen Chemischen Gesellschaft zu Berlin. 23 (2): 3023–3033. doi:10.1002/cber.189002302232.
  • Curtius, T. (1894). "20. Hydrazide und Azide organischer Säuren I. Abhandlung" [Hydrazides and azides of organic acids I. paper]. Journal für Praktische Chemie. 50: 275–294. doi:10.1002/prac.18940500125.
  • Scriven, Eric F. V.; Turnbull, Kenneth (1988). "Azides: their preparation and synthetic uses". Chemical Reviews. 88 (2): 297–368. doi:10.1021/cr00084a001.
  • Weinstock, J (1961). "Modified Curtius reaction". J. Org. Chem. 26: 3511. doi:10.1021/jo01067a604.
  • Warren, J. D.; Press, J. B. (1980). "Formation and Curtius rearrangement of acyl azides from unreactive acid chlorides". Synth. Commun. 10: 107–110. doi:10.1080/00397918008061812.
  • Pozsgay, V.; Jennings, H. J. (1987). "Azide synthesis with stable nitrosyl salts". Tetrahedron Lett. 28 (43): 5091–5092. doi:10.1016/s0040-4039(00)95598-9.
  • Shioiri, T.; Ninomiya, K.; Yamada, S. (1972). "New convenient reagent for a modified Curtius reaction and for peptide synthesis". J. Am. Chem. Soc. 94 (17): 6203–6205. doi:10.1021/ja00772a052. PMID 5054412.
  • Rauk, A.; Alewood, P. F. (1977). "A theoretical study of the Curtius rearrangement. The electronic structures and interconversion of the CHNO species". Can. J. Chem. 55 (9): 1498–1510. doi:10.1139/v77-209.
  • L'Abbe, G. (1969). "Decomposition and addition reactions of organic azides". Chem. Rev. 69 (3): 345–363. doi:10.1021/cr60259a004.
  • Yukawa, Y.; Tsuno, Y. (1959). "The decomposition of substituted benzazides in acidic solvents, the acid catalysis". J. Am. Chem. Soc. 81: 2007–2012. doi:10.1021/ja01517a055.
  • Fahr, E.; Neumann, L. (1965). "Curtius-Reaktion mit Bortrihalogeniden". Angew. Chem. 77 (13): 591. Bibcode:1965AngCh..77..591F. doi:10.1002/ange.19650771308.
  • Wentrup, C.; Bornemann, H. (2005). "Curtius rearrangment of acyl azides revisited - formation of cyanate". Eur. J. Org. Chem.: 4521–4524. doi:10.1002/ejoc.200500545.
  • Eibler, E.; Sauer, J. (1974). "Ein Betrag zur Isocyanatbildung bei der Photolyse von Acylaziden". Tetrahedron Lett. 15 (30): 2569–2572. doi:10.1016/s0040-4039(01)92295-6.
  • Gagnon, P. E.; Bovin, P. A.; Craig, H. M. (1951). "Synthesis of amino acids from substituted cyanoacetic esters". Can. J. Chem. 29: 70–75. doi:10.1139/cjc-29-1-70.
  • Bertrand, G.; Majoral, J.; Baceiredo, A. (1980). "Photolytic rearrangement of phosphorus azide: evidence for a transient metaphosphonimidate". Tetrahedron Lett. 21 (52): 5015–5018. doi:10.1016/s0040-4039(00)71119-1.
  • Harger, M. J. P.; Westlake, S. (1982). "Photolysis of some unsymmetrical phosphinic azides in methanol". Tetrahedron. 38 (20): 3073–3078. doi:10.1016/0040-4020(82)80195-6.
  • Harger, M. J. P.; Westlake, S. (1982). "Photolysis of some unsymmetrical phosphinic azides in methanol". Tetrahedron. 38 (20): 3073–3078. doi:10.1016/0040-4020(82)80195-6.
  • Am Ende, David J.; Devries, Keith M.; Clifford, Pamela J.; Brenek, Steven J. (1998). "A Calorimetric Investigation to Safely Scale-Up a Curtius Rearrangement of Acryloyl Azide". Organic Process Research & Development. 2 (6): 382–392. doi:10.1021/op970115w.
  • Lebel, H.; Leogane, O. (2005). "Boc-protected amines via a mild and efficient one-pot Curtius rearrangement". Organic Letters. 7 (19): 4107–4110. doi:10.1021/ol051428b. PMID 16146363.
  • Woodward, R. B.; Fukunaga, T.; Kelly, R. C. (1964). "Triquinacene". J. Am. Chem. Soc. 86 (15): 3162–3164. doi:10.1021/ja01069a046.
  • Ishikawa, H.; Suzuki, T.; Hayashi, Y. (2009). "High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations". Angew. Chem. Int. Ed. 48 (7): 1304–1307. doi:10.1002/anie.200804883. PMID 19123206.
  • Unsworth, William P.; Kitsiou, Christiana; Taylor, Richard J. K. (5 July 2013). "An Expedient Protecting-Group-Free Total Synthesis of (±)-Dievodiamine". Organic Letters. 15 (13): 3302–3305. doi:10.1021/ol4013469. PMID 23786450.

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  • Shioiri, T.; Ninomiya, K.; Yamada, S. (1972). "New convenient reagent for a modified Curtius reaction and for peptide synthesis". J. Am. Chem. Soc. 94 (17): 6203–6205. doi:10.1021/ja00772a052. PMID 5054412.
  • Lebel, H.; Leogane, O. (2005). "Boc-protected amines via a mild and efficient one-pot Curtius rearrangement". Organic Letters. 7 (19): 4107–4110. doi:10.1021/ol051428b. PMID 16146363.
  • Ishikawa, H.; Suzuki, T.; Hayashi, Y. (2009). "High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations". Angew. Chem. Int. Ed. 48 (7): 1304–1307. doi:10.1002/anie.200804883. PMID 19123206.
  • Unsworth, William P.; Kitsiou, Christiana; Taylor, Richard J. K. (5 July 2013). "An Expedient Protecting-Group-Free Total Synthesis of (±)-Dievodiamine". Organic Letters. 15 (13): 3302–3305. doi:10.1021/ol4013469. PMID 23786450.

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