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Wolff–Kishner reduction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Wolff–Kishner reduction" in English language version.

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39doi.org
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1books.google.com
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  • Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 1835, ISBN 978-0-471-72091-1

doi.org

  • Wolff, L. (1912). "Chemischen Institut der Universität Jena: Methode zum Ersatz des Sauerstoffatoms der Ketone und Aldehyde durch Wasserstoff. [Erste Abhandlung]". Justus Liebig's Annalen der Chemie. 394: 86–108. doi:10.1002/jlac.19123940107.
  • Lewis, D. E. (2013). "Disability, Despotism, Deoxygenation-From Exile to Academy Member: Nikolai Matveevich Kizhner". Angewandte Chemie International Edition. 52 (45): 11704–11712. doi:10.1002/anie.201303165. PMID 24123691.
  • Herr, C. H.; Whitmore, F. C.; Schiessler, R. W. (1945). "The Wolff-Kishner Reaction at Atmospheric Pressure". Journal of the American Chemical Society. 67 (12): 2061. doi:10.1021/ja01228a002.
  • Soffer, M. D.; Soffer, M. B.; Sherk, K. W. (1945). "A Low Pressure Method for Wolff—Kishner Reduction". Journal of the American Chemical Society. 67 (9): 1435. doi:10.1021/ja01225a004.
  • Szmant, H. H.; Harmuth, C. M. (1964). "The Wolff-Kishner Reaction of Hydrazones". Journal of the American Chemical Society. 86 (14): 2909. doi:10.1021/ja01068a028.
  • Szmant, H. H. (1968). "The Mechanism of the Wolff-Kishner Reduction, Elimination, and Isomerization Reactions". Angewandte Chemie International Edition in English. 7 (2): 120–128. doi:10.1002/anie.196801201.
  • Szmant, H. H.; Roman, M. N. (1966). "The Effect of Dimethyl Sulfoxide on the Rate of the Wolff-Kishner Reaction of Benzophenone Hydrazone1". Journal of the American Chemical Society. 88 (17): 4034. doi:10.1021/ja00969a025.
  • Szmant, H. H.; Alciaturi, C. E. (1977). "Mechanistic aspects of the Wolff-Kishner reaction. 6. Comparison of the hydrazones of benzophenone, fluorenone, dibenzotropone, and dibenzosuberone". The Journal of Organic Chemistry. 42 (6): 1081. doi:10.1021/jo00426a034.
  • Szmant, H. H.; Harnsberger, H. F.; Butler, T. J.; Barie, W. P. (1952). "Kinetics of the Wolff-Kishner Reaction of Diaryl Ketone Hydrazones". Journal of the American Chemical Society. 74 (11): 2724. doi:10.1021/ja01131a009.
  • Taber, D. F.; Stachel, S. J. (1992). "On the mechanism of the Wolff-Kishner reduction". Tetrahedron Letters. 33 (7): 903. doi:10.1016/S0040-4039(00)91571-5.
  • Huang-Minlon, [N. A. (1946). "A Simple Modification of the Wolff-Kishner Reduction". Journal of the American Chemical Society. 68 (12): 2487–2488. doi:10.1021/ja01216a013.
  • Osdene, T. S.; Timmis, G. M.; Maguire, M. H.; Shaw, G.; Goldwhite, H.; Saunders, B. C.; Clark, E. R.; Epstein, P. F.; Lamchen, M.; Stephen, A. M.; Tipper, C. F. H.; Eaborn, C.; Mukerjee, S. K.; Seshadri, T. R.; Willenz, J.; Robinson, R.; Thomas, A. F.; Hickman, J. R.; Kenyon, J.; Crocker, H. P.; Hall, R. H.; Burnell, R. H.; Taylor, W. I.; Watkins, W. M.; Barton, D. H. R.; Ives, D. A. J.; Thomas, B. R. (1955). "Notes". Journal of the Chemical Society (Resumed): 2038. doi:10.1039/JR9550002038.
  • Cram, D. J.; Sahyun, M. R. V. (1962). "Room Temperature Wolff-Kishner Reduction and Cope Elimination Reactions". Journal of the American Chemical Society. 84 (9): 1734. doi:10.1021/ja00868a048.
  • Grundon, M. F.; Henbest, H. B.; Scott, M. D. (1963). "344. The reactions of hydrazones and related compounds with strong bases. Part I. A modified Wolff?Kishner procedure". Journal of the Chemical Society (Resumed): 1855–1858. doi:10.1039/JR9630001855.
  • Caglioti, L.; Magi, M. (1963). "The reaction of tosylhydrazones with lithium aluminium hydride". Tetrahedron. 19 (7): 1127. doi:10.1016/S0040-4020(01)98571-0.
  • Furrow, M. E.; Myers, A. G. (2004). "Practical Procedures for the Preparation ofN-tert-Butyldimethylsilylhydrazones and Their Use in Modified Wolff−Kishner Reductions and in the Synthesis of Vinyl Halides andgem-Dihalides". Journal of the American Chemical Society. 126 (17): 5436–5445. doi:10.1021/ja049694s. PMID 15113215.
  • Huang-Minlon, [N. A. . (1949). "Reduction of Steroid Ketones and other Carbonyl Compounds by Modified Wolff--Kishner Method". Journal of the American Chemical Society. 71 (10): 3301–3303. doi:10.1021/ja01178a008.
  • Leonard, N. J.; Gelfand, S. (1955). "The Kishner Reduction-Elimination. II. α-Substituted Pinacolones1,2". Journal of the American Chemical Society. 77 (12): 3272. doi:10.1021/ja01617a036.
  • Caglioti, L. (1966). "The reduction of tosylhydrazones and of acyl tosylhydrazides". Tetrahedron. 22 (2): 487–493. doi:10.1016/0040-4020(66)80015-7.
  • Hutchins, R. O.; Milewski, C. A.; Maryanoff, B. E. (1973). "Selective deoxygenation of ketones and aldehydes including hindered systems with sodium cyanoborohydride". Journal of the American Chemical Society. 95 (11): 3662. doi:10.1021/ja00792a033.
  • Miller, V. P.; Yang, D. Y.; Weigel, T. M.; Han, O.; Liu, H. W. (1989). "Studies of the mechanistic diversity of sodium cyanoborohydride reduction of tosylhydrazones". The Journal of Organic Chemistry. 54 (17): 4175. doi:10.1021/jo00278a035.
  • Bosch, J.; Bonjoch, J. (1981). "Synthetic route to 6-functionalized 2-azabicyclo\3.3.1]nonanes". The Journal of Organic Chemistry. 46 (8): 1538. doi:10.1021/jo00321a004.
  • Hutchins, R. O.; Kacher, M.; Rua, L. (1975). "Synthetic utility and mechanism of the reductive deoxygenation of .alpha.,.beta.-unsaturated p-tosylhydrazones with sodium cyanoborohydride". The Journal of Organic Chemistry. 40 (7): 923. doi:10.1021/jo00895a024.
  • Kabalka, G. W.; Yang, D. T. C.; Baker, J. D. (1976). "Deoxygenation of .alpha.,.beta.-unsaturated aldehydes and ketones via the catecholborane reduction of the corresponding tosylhydrazones". The Journal of Organic Chemistry. 41 (3): 574. doi:10.1021/jo00865a043.
  • Taylor, E. J.; Djerassi, C. (1976). "Mechanism of the sodium cyanoborohydride reduction of .alpha.,.beta.-unsaturated tosylhydrazones". Journal of the American Chemical Society. 98 (8): 2275. doi:10.1021/ja00424a046.
  • Qi, W.; McIntosh, M. C. (2008). "Acyclic 1,4-Stereocontrol via Reductive 1,3-Transpositions". Organic Letters. 10 (2): 357–359. doi:10.1021/ol702921x. PMC 2613761. PMID 18092798.
  • Eisenlohr, F.; Polenske, R. (1924). "Über die raumisomeren Formen des Dekahydro-naphthalins (Dekalins)". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 57 (9): 1639. doi:10.1002/cber.19240570902.
  • Leonard, N. J.; Gelfand, S. (1955). "The Kishner Reduction-Elimination. I. Cyclic and Open Chain α-Aminoketones1,2". Journal of the American Chemical Society. 77 (12): 3269. doi:10.1021/ja01617a035.
  • Wharton, P.; Bohlen, D. (1961). "Communications- Hydrazine Reduction of α, β-Epoxy Ketones to Allylic Alcohols". The Journal of Organic Chemistry. 26 (9): 3615. doi:10.1021/jo01067a117.
  • Gustafson, D. H.; Erman, W. F. (1965). "A Novel Fragmentation of trans-π-Bromocamphor". The Journal of Organic Chemistry. 30 (5): 1665. doi:10.1021/jo01016a516.
  • Kupchan, S. M.; Abushanab, E.; Shamasundar, K. T.; By, A. W. (1967). "Buxus alkaloids. 13. A synthetic approach to the 9(10--19) abeo-pregnane system". Journal of the American Chemical Society. 89 (24): 6327–6332. doi:10.1021/ja01000a060. PMID 6066048.
  • Overman, L. E.; Ricca, D. J.; Tran, V. D. (1993). "First total synthesis of scopadulcic acid B". Journal of the American Chemical Society. 115 (5): 2042. doi:10.1021/ja00058a064.
  • Marino, J. P.; Rubio, M. B.; Cao, G.; De Dios, A. (2002). "Total Synthesis of (+)-Aspidospermidine: A New Strategy for the Enantiospecific Synthesis of Aspidosperma Alkaloids". Journal of the American Chemical Society. 124 (45): 13398–13399. doi:10.1021/ja026357f. PMID 12418888.
  • Kawano, M.; Kiuchi, T.; Negishi, S.; Tanaka, H.; Hoshikawa, T.; Matsuo, J. I.; Ishibashi, H. (2013). "Regioselective Inter- and Intramolecular Formal \4+2] Cycloaddition of Cyclobutanones with Indoles and Total Synthesis of (±)-Aspidospermidine". Angewandte Chemie International Edition. 52 (3): 906–10. doi:10.1002/anie.201206734. PMID 23184896.
  • Miyaoka, H.; Kajiwara, Y.; Hara, Y.; Yamada, Y. (2001). "Total Synthesis of Natural Dysidiolide". The Journal of Organic Chemistry. 66 (4): 1429–1435. doi:10.1021/jo0015772. PMID 11312976.
  • Bashore, C. G.; Samardjiev, I. J.; Bordner, J.; Coe, J. W. (2003). "Twisted Amide Reduction under Wolff−Kishner Conditions: Synthesis of a Benzo-1-Aza-Adamantane Derivative". Journal of the American Chemical Society. 125 (11): 3268–3272. doi:10.1021/ja028152c. PMID 12630882.
  • Green, J. C.; Pettus, T. R. R. (2011). "An Oxidative Dearomatization-Induced \5 + 2] Cascade Enabling the Syntheses of α-Cedrene, α-Pipitzol, andsec-Cedrenol". Journal of the American Chemical Society. 133 (5): 1603–1608. doi:10.1021/ja109925g. PMID 21194216.
  • Kuethe, J. T.; Childers, K. G.; Peng, Z.; Journet, M.; Humphrey, G. R.; Vickery, T.; Bachert, D.; Lam, T. T. (2009). "A Practical, Kilogram-Scale Implementation of the Wolff−Kishner Reduction". Organic Process Research & Development. 13 (3): 576. doi:10.1021/op9000274.
  • Hutchison, John M.; Gibson, Andrew S.; Williams, David T.; McIntosh, Matthias C. (2011). "Synthesis of the C21–C34 fragment of antascomicin B". Tetrahedron Letters. 52 (48): 6349–6351. doi:10.1016/j.tetlet.2011.09.027. ISSN 0040-4039. PMC 3244276. PMID 22199407.

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