(E)-stilben (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "(E)-stilben" in Czech language version.

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archive.org

Ernest L. Eliel; Samuel H. Wilen. Stereochemistry of Organic Compounds. [s.l.]: John Wiley and Sons, 1994. Dostupné online. ISBN 0-471-01670-5. S. 566–567.
David Lide. CRC Handbook of Chemistry and Physics. [s.l.]: CRC Press, 1995. Dostupné online. ISBN 0-8493-0476-8.
William M. Cumming; I. Vance Hopper; T. Sherlock Wheeler. Systematic Organic Chemistry: Modern Methods of Preparation and Estimation. New York: D. Van Nostrand Company, 1926. Kapitola Preparation 294.—Dinitro-Stilbene-Disulphonic Acid (Na salt).

doi.org

BUCKLES, Robert E.; WHEELER, Norris G. cis-Stilbene. Org. Synth.. 1953, s. 88. Dostupné online. doi:10.15227/orgsyn.033.0088. ; Coll. Vol.. S. 857.
SHRINER, R. L.; BERGER, Alfred. trans-Stilbene. Org. Synth.. 1943, s. 86. Dostupné online. doi:10.15227/orgsyn.023.0086. ; Coll. Vol.. S. 786.
R. F. Heck; J. P. Nolley. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides. The Journal of Organic Chemistry. 1972, s. 2320–2322. doi:10.1021/jo00979a024.
Tsutomu Mizoroki; Kunio Mori; Atsumu Ozaki. Arylation of Olefin with Aryl Iodide Catalyzed by Palladium. Bulletin of the Chemical Society of Japan. 1971, s. 581. doi:10.1246/bcsj.44.581.
Richard F. Heck. Palladium-catalyzed vinylation of organic halides. Organic Reactions. 1982, s. 345–390. ISBN 0471264180. doi:10.1002/0471264180.or027.02.
Irina P. Beletskaya; Andrei V. Cheprakov. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chemical Reviews. 2000, s. 3009–3066. doi:10.1021/cr9903048. PMID 11749313.
Yoshiro Ogata; Kohtaro Tomizawa; Toshiyuki Ikeda. Oxidation of trans-stilbene with peroxymonophosphoric acid. The Journal of Organic Chemistry. 1979, s. 2362–2364. doi:10.1021/jo01328a006.
Guochuan Yin; Andrew M. Danby; David Kitko; John D. Carter; William M. Scheper; Daryle H. Busch. Olefin Epoxidation by Alkyl Hydroperoxide with a Novel Cross-Bridged Cyclam Manganese Complex: Demonstration of Oxygenation by Two Distinct Reactive Intermediates. Inorganic Chemistry. 2007, s. 2173–2180. doi:10.1021/ic061957r.
Han-Ting Chang; K. Barry Sharpless. Molar Scale Synthesis of Enantiopure Stilbene Oxide. The Journal of Organic Chemistry. 1996, s. 6456–6457. doi:10.1021/jo960718q. PMID 11667495.
Clyde E. Bishop; Donald D. Denson; Paul R. Story. Mechanisms of ozonolysis. The cis, trans-stilbene system. Tetrahedron Letters. 1968, s. 5739–5742. doi:10.1016/S0040-4039(00)76338-6.
Eric N. Jacobsen; Istvan Marko; William S. Mungall; Georg Schroeder; K. Barry Sharpless. Asymmetric dihydroxylation via ligand-accelerated catalysis. Journal of the American Chemical Society. 1988, s. 1968–1970. doi:10.1021/ja00214a053.
Hartmuth C. Kolb; Michael S. VanNieuwenhze; K. Barry Sharpless. Asymmetric dihydroxylation via ligand-accelerated catalysis. Chemical Reviews. 1994, s. 2483–2547. doi:10.1021/cr00032a009.
Zhi-Min Wang; K. Barry Sharpless. A Solid-to-Solid Asymmetric Dihydroxylation Procedure for Kilogram-Scale Preparation of Enantiopure Hydrobenzoin. The Journal of Organic Chemistry. 1994, s. 8302–8303. doi:10.1021/jo00105a065.
MCKEE, Blaine H.; GILHEANY, Declan G.; SHARPLESS, K. Barry. (R,R)-1,2-Diphenyl-1,2-ethanediol (Stilbene Diol). Org. Synth.. 1992, s. 47. Dostupné online. doi:10.15227/orgsyn.070.0047. ; Coll. Vol.. S. 383.
Robert E. Buckles; Jane M. Bader; Roland J. Thurmaier. Stereospecificity of the Addition of Bromine to cis- and trans-Stilbene. The Journal of Organic Chemistry. 1962, s. 4523–4527. doi:10.1021/jo01059a097.
Roberto Bianchini; Cinzia Chiappe. Stereoselectivity and reversibility of electrophilic bromine addition to stilbenes in chloroform: influence of the bromide-tribromide-pentabromide equilibrium in the counteranion of the ionic intermediates. The Journal of Organic Chemistry. 1992, s. 6474–6478. doi:10.1021/jo00050a021.
S. P. Kwasniewski; L. Claes; J.-P. François; M. S. Deleuze. High level theoretical study of the structure and rotational barriers of trans-stilbene. The Journal of Chemical Physics. 2003, s. 7823–7836. doi:10.1063/1.1563617. Bibcode 2003JChPh.118.7823K.
Peter F. Vogt; John J. Gerulis. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH, 2000. ISBN 3527306730. doi:10.1002/14356007.a02_037. Kapitola Amines, Aromatic.
Klaus Hunger; Peter Mischke; Wolfgang Rieper; Roderich Raue; Klaus Kunde; Aloys Engel. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH, 2005. ISBN 3527306730. doi:10.1002/14356007.a03_245. Kapitola Azo Dyes.
Arthur G. Green. Ueber die Oxydation von Paranitrotoluolsulfosäure. Berichte der Deutschen Chemischen Gesellschaft. 1897, s. 3097–3101. Dostupné online. doi:10.1002/cber.189703003128.

harvard.edu

adsabs.harvard.edu

S. P. Kwasniewski; L. Claes; J.-P. François; M. S. Deleuze. High level theoretical study of the structure and rotational barriers of trans-stilbene. The Journal of Chemical Physics. 2003, s. 7823–7836. doi:10.1063/1.1563617. Bibcode 2003JChPh.118.7823K.

nih.gov

ncbi.nlm.nih.gov

Irina P. Beletskaya; Andrei V. Cheprakov. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chemical Reviews. 2000, s. 3009–3066. doi:10.1021/cr9903048. PMID 11749313.
Han-Ting Chang; K. Barry Sharpless. Molar Scale Synthesis of Enantiopure Stilbene Oxide. The Journal of Organic Chemistry. 1996, s. 6456–6457. doi:10.1021/jo960718q. PMID 11667495.

pubchem.ncbi.nlm.nih.gov

https://pubchem.ncbi.nlm.nih.gov/compound/638088

orgsyn.org

BUCKLES, Robert E.; WHEELER, Norris G. cis-Stilbene. Org. Synth.. 1953, s. 88. Dostupné online. doi:10.15227/orgsyn.033.0088. ; Coll. Vol.. S. 857.
SHRINER, R. L.; BERGER, Alfred. trans-Stilbene. Org. Synth.. 1943, s. 86. Dostupné online. doi:10.15227/orgsyn.023.0086. ; Coll. Vol.. S. 786.
MCKEE, Blaine H.; GILHEANY, Declan G.; SHARPLESS, K. Barry. (R,R)-1,2-Diphenyl-1,2-ethanediol (Stilbene Diol). Org. Synth.. 1992, s. 47. Dostupné online. doi:10.15227/orgsyn.070.0047. ; Coll. Vol.. S. 383.

patents.google.com

Process for the preparation of 4,4'-dinitrostilbene-2,2-disulfonic acid. Původce vynálezu: Guglielmetti LEONARDO. US. Patentový spis US5041632A. 1991-08-20. Dostupné: <online> [cit. 2022-10-17].

zenodo.org

Arthur G. Green. Ueber die Oxydation von Paranitrotoluolsulfosäure. Berichte der Deutschen Chemischen Gesellschaft. 1897, s. 3097–3101. Dostupné online. doi:10.1002/cber.189703003128.