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Curtiův přesmyk (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Curtiův přesmyk" in Czech language version.

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23doi.org
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4nih.gov
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2orgsyn.org
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1bnf.fr
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  • CURTIUS, Theodor. Ueber Stickstoffwasserstoffsäure (Azoimid) N3H. Berichte der Deutschen Chemischen Gesellschaft zu Berlin. Roč. 23, čís. 2, s. 3023–3033. Dostupné online. doi:10.1002/cber.189002302232. (německy) 

doi.org

  • CURTIUS, Theodor. Ueber Stickstoffwasserstoffsäure (Azoimid) N3H. Berichte der Deutschen Chemischen Gesellschaft zu Berlin. Roč. 23, čís. 2, s. 3023–3033. Dostupné online. doi:10.1002/cber.189002302232. (německy) 
  • CURTIUS, Theodor. 20. Hydrazide und Azide organischer Säuren I. Abhandlung. Journal für Praktische Chemie. Roč. 50, s. 275–29. Dostupné online. doi:10.1002/prac.18940500125. (německy) 
  • KAISER, C.; WEINSTOCK, J. Amines from mixed carboxylic-carbonic anhydrides: 1-phenylcyclopentylamine. Organic Syntheses. S. 910. Dostupné online. doi:10.15227/orgsyn.051.0048. 
  • SCRIVEN, Eric F. V.; TURNBUL, Kenneth. Azides: their preparation and synthetic uses. Chemical Reviews. Roč. 88, čís. 2, s. 297–368. doi:10.1021/cr00084a001. 
  • WEINSTOCK, J. Modified Curtius reaction. Org. Chem.. Roč. 26, s. 3511. doi:10.1021/jo01067a604. 
  • WARREN, J. D.; PRESS, J. B. Formation and Curtius rearrangement of acyl azides from unreactive acid chlorides. Synth. Commun.. Roč. 10, s. 107–110. doi:10.1080/00397918008061812. 
  • POZSGAY, V.; JENNINGS, H. J. Azide synthesis with stable nitrosyl salts. Tetrahedron Lett. Roč. 28, čís. 43, s. 5091–5092. doi:10.1016/s0040-4039(00)95598-9. 
  • SHIORI, T.; NINOMIYA, K.; YAMADA, S. New convenient reagent for a modified Curtius reaction and for peptide synthesis. J. Am. Chem. Soc. Roč. 94, čís. 17, s. 6203–620. doi:10.1021/ja00772a052. PMID 5054412. 
  • RAUK, A.; ALEWOOD, P. F. A theoretical study of the Curtius rearrangement. The electronic structures and interconversion of the CHNO species. Can. J. Chem.. Roč. 55, čís. 9, s. 1498–1510. doi:10.1139/v77-209. 
  • L'ABBE, G. Decomposition and addition reactions of organic azides. Chem. Rev.. Roč. 69, čís. 3, s. 345–363. doi:10.1021/cr60259a004. 
  • YUKAWA, Y.; TSUNO, Y. The decomposition of substituted benzazides in acidic solvents, the acid catalysi. J. Am. Chem. Soc.. Roč. 81, s. 2007–2012. doi:10.1021/ja01517a055. 
  • FAHR, E.; NEUMANN, L. Curtius-Reaktion mit Bortrihalogeniden. Angew. Chem.. Roč. 77, čís. 13, s. 591. doi:10.1002/ange.19650771308. 
  • WENTRUP, C.; BORNEMANN, H. Curtius rearrangment of acyl azides revisited - formation of cyanate. Eur. J. Org. Chem. S. 4521–4524. doi:10.1002/ejoc.200500545. 
  • EIBLER, E.; SAUER, J. Ein Betrag zur Isocyanatbildung bei der Photolyse von Acylaziden. Tetrahedron Lett. Roč. 15, čís. 30, s. 2569–2572. doi:10.1016/s0040-4039(01)92295-6. 
  • GAGNON, P. E.; BOVIN, P. A.; CRAIG, H. M. Synthesis of amino acids from substituted cyanoacetic esters. Can. J. Chem.. Roč. 29, s. 70–75. doi:10.1139/cjc-29-1-70. 
  • BERTRAND, G.; MAJORAL, J.; BACEIREDO, A. Photolytic rearrangement of phosphorus azide: evidence for a transient metaphosphonimidate. Tetrahedron Lett. Roč. 21, čís. 52, s. 5015–5018. doi:10.1016/s0040-4039(00)71119-1. 
  • HARGER, M. J. P.; WESTLAKE, S. Photolysis of some unsymmetrical phosphinic azides in methanol. Tetrahedron. Roč. 38, čís. 20, s. 3073–3078. doi:10.1016/0040-4020(82)80195-6. 
  • HARGER, M. J. P.; WESTLAKE, S. Photolysis of some unsymmetrical phosphinic azides in methanol. Tetrahedron. Roč. 38, čís. 20. doi:10.1016/0040-4020(82)80195-6. 
  • AM ENDE, David J.; DEVRIES, Keith M.; CLIFFORD, Pamela J., Steven J. Brenek. A Calorimetric Investigation to Safely Scale-Up a Curtius Rearrangement of Acryloyl Azide. Organic Process Research & Development. Roč. 2, čís. 6, s. 382–392. doi:10.1021/op970115w. 
  • LEBEL, H.; LEOGANE, O. Boc-protected amines via a mild and efficient one-pot Curtius rearrangement. Organic Letters. Roč. 7, čís. 19, s. 4107–4110. doi:10.1021/ol051428b. PMID 16146363. 
  • JESSUP, P. J.; PETTY, C. B.; ROOS, J., L. E. Overman. 1-N-ACYLAMINO-1,3-DIENES FROM 2,4-PENTADIENOIC ACIDS BY THE CURTIUS REARRANGEMENT: BENZYL trans-1,3-BUTADIENE-1-CARBAMATE. Organic Syntheses. Dostupné online. doi:10.15227/orgsyn.059.0001. 
  • H., Ishikawa; SUZUKI, T.; HAYASHI, H. High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations. Angew. Chem. Int. Ed. Roč. 48, čís. 7, s. 1304–1307. doi:10.1002/anie.200804883. PMID 19123206. 
  • UNSWORTH, William P.; KITSIOU, Christiana; TAYLOR, Richard J. K. An Expedient Protecting-Group-Free Total Synthesis of (±)-Dievodiamine. Organic Letters. Roč. 15, čís. 13, s. 3302–3305. doi:10.1021/ol4013469. PMID 23786450. 

nih.gov

ncbi.nlm.nih.gov

  • SHIORI, T.; NINOMIYA, K.; YAMADA, S. New convenient reagent for a modified Curtius reaction and for peptide synthesis. J. Am. Chem. Soc. Roč. 94, čís. 17, s. 6203–620. doi:10.1021/ja00772a052. PMID 5054412. 
  • LEBEL, H.; LEOGANE, O. Boc-protected amines via a mild and efficient one-pot Curtius rearrangement. Organic Letters. Roč. 7, čís. 19, s. 4107–4110. doi:10.1021/ol051428b. PMID 16146363. 
  • H., Ishikawa; SUZUKI, T.; HAYASHI, H. High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations. Angew. Chem. Int. Ed. Roč. 48, čís. 7, s. 1304–1307. doi:10.1002/anie.200804883. PMID 19123206. 
  • UNSWORTH, William P.; KITSIOU, Christiana; TAYLOR, Richard J. K. An Expedient Protecting-Group-Free Total Synthesis of (±)-Dievodiamine. Organic Letters. Roč. 15, čís. 13, s. 3302–3305. doi:10.1021/ol4013469. PMID 23786450. 

orgsyn.org

web.archive.org

zenodo.org