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29 reactions in Reaxys
2016-06-14 18h:30m:01s (EST)
29 reactions in Reaxys
2016-06-14 18h:30m:18s (EST)
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(1. Query) AND itemno in (1)
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Br
Cl
Cl
Rx-ID: 10186902 View in Reaxys 1/29 Yield
Conditions & References Stage 1: With iodine, magnesium in diethyl ether, Time= 2h, T= 40 °C Stage 2: With bis(1,3-diphenylphosphinopropane) nickel(II) chloride in diethyl ether, Time= 8h, Further stages. Peng; Chen; Fann; Journal of the American Chemical Society; vol. 123; nb. 46; (2001); p. 11388 - 11397 View in Reaxys
Rx-ID: 824409 View in Reaxys 2/29 Yield
Conditions & References With sulfuric acid, T= 3 - 18 °C Buu-Hoi; Cagniant; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 216; (1943); p. 381 View in Reaxys Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys With aluminium trichloride, T= 3 - 18 °C Buu-Hoi; Cagniant; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 216; (1943); p. 381 View in Reaxys Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys
HO
Rx-ID: 824793 View in Reaxys 3/29 Yield
Conditions & References With aluminium trichloride Zukerwanik; Ssidorowa; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 641,642; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 579 View in Reaxys With boron trifluoride, T= 60 °C McKenna; Sowa; Journal of the American Chemical Society; vol. 59; (1937); p. 470 View in Reaxys
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O
O
Rx-ID: 847883 View in Reaxys 4/29 Yield
Conditions & References With boron trifluoride McKenna; Sowa; Journal of the American Chemical Society; vol. 59; (1937); p. 1204 View in Reaxys
HO
Rx-ID: 847951 View in Reaxys 5/29 Yield
Conditions & References With aluminium trichloride Buu-Hoi; Cagniant; Palfray; Bulletin de la Societe Chimique de France; vol. <5> 12; (1945); p. 975,977 View in Reaxys Huston; Goodemoot; Journal of the American Chemical Society; vol. 56; (1934); p. 2432 View in Reaxys
Cl
Rx-ID: 847857 View in Reaxys 6/29 Yield
Conditions & References With carbon disulfide, aluminium trichloride, T= 40 - 50 °C Hueckel; Bretschneider; Justus Liebigs Annalen der Chemie; vol. 540; (1939); p. 157,180 View in Reaxys Neunhoeffer; Journal fuer Praktische Chemie (Leipzig); vol. <2> 133; (1932); p. 95,105 View in Reaxys
Cl
Cl
Br Mg
Rx-ID: 1418504 View in Reaxys 7/29 Yield
Conditions & References With nickel Tamao,K. et al.; Bulletin of the Chemical Society of Japan; vol. 49; (1976); p. 1958 - 1969 View in Reaxys
Br
Rx-ID: 846684 View in Reaxys 8/29 Yield
Conditions & References With carbon disulfide, aluminium trichloride v. Braun; Chemische Berichte; vol. 60; (1927); p. 1180 View in Reaxys
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HO
Rx-ID: 4062661 View in Reaxys 9/29 Yield
Conditions & References With sulfuric acid Novikov,I.N.; Zavgorodnii,S.V.; Doklady Chemistry; vol. 148; (1963); p. 111 - 113; Doklady Akademii Nauk SSSR; vol. 148; (1963); p. 853 - 855 View in Reaxys
1,3-dicyclohexyl-benzene, cyclohexylbenzene
Cl
Rx-ID: 7027009 View in Reaxys 10/29 Yield
Conditions & References With aluminium Turowa-Poljak; Dawydowa; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 2710,2713; engl. Ausg. S. 3019, 3021 View in Reaxys
HO
Rx-ID: 824794 View in Reaxys 11/29 Yield
Conditions & References With phosphorous pentafluoride Patent; Standard Oil Co. of Indiana; US2767230; (1954) View in Reaxys
OH HO
S OO
1.2.3.5-tetracyclohexyl-benzene Rx-ID: 7156440 View in Reaxys 12/29 Yield
Conditions & References T= 2 - 14 °C Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys
OH HO
S OO
Rx-ID: 7432752 View in Reaxys 13/29 Yield
Conditions & References T= 2 - 14 °C
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Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys
Cl Al
Cl
Cl
Rx-ID: 7449743 View in Reaxys 14/29 Yield
Conditions & References T= 80 - 85 °C Corson; Ipatieff; Journal of the American Chemical Society; vol. 60; (1938); p. 747 View in Reaxys O
O S O
Rx-ID: 1051362 View in Reaxys 15/29 Yield
Conditions & References Blackwell,J.; Hickinbottom,W.J.; Journal of the Chemical Society; (1963); p. 518 - 523 View in Reaxys
Cl Al
Cl
Cl
1.2.3.5-tetracyclohexyl-benzene
Rx-ID: 5811544 View in Reaxys 16/29 Yield
Conditions & References Truffault; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 202; (1936); p. 1286; Bulletin de la Societe Chimique de France; vol. <5> 6; (1939); p. 726,730 View in Reaxys Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys
OH HO
S OO
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1.2.3.5-tetracyclohexyl-benzene
Rx-ID: 5811545 View in Reaxys 17/29 Yield
Conditions & References Truffault; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 202; (1936); p. 1286; Bulletin de la Societe Chimique de France; vol. <5> 6; (1939); p. 726,730 View in Reaxys Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys Corson; Ipatieff; Journal of the American Chemical Society; vol. 59; (1937); p. 645; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 151 View in Reaxys HO
Cl Al
Cl
Cl
Rx-ID: 6674942 View in Reaxys 18/29 Yield
Conditions & References Buu-Hoi; Cagniant; Palfray; Bulletin de la Societe Chimique de France; vol. <5> 12; (1945); p. 975,977 View in Reaxys Huston; Goodemoot; Journal of the American Chemical Society; vol. 56; (1934); p. 2432 View in Reaxys
F B
F
HO
F
polycyclohexyl-benzene Rx-ID: 6730794 View in Reaxys 19/29 Yield
Conditions & References McKenna; Sowa; Journal of the American Chemical Society; vol. 59; (1937); p. 470 View in Reaxys
O
O
F B
F
F
Rx-ID: 7159192 View in Reaxys 20/29 Yield
Conditions & References McKenna; Sowa; Journal of the American Chemical Society; vol. 59; (1937); p. 1204 View in Reaxys
S
S
Cl Al
Cl
Cl
Cl
tetracyclohexyl-benzene Rx-ID: 6731645 View in Reaxys 21/29
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Yield
Conditions & References T= 40 - 50 °C Hueckel; Bretschneider; Justus Liebigs Annalen der Chemie; vol. 540; (1939); p. 157,180 View in Reaxys
palladium Rx-ID: 7156439 View in Reaxys 22/29 Yield
Conditions & References Hydrogenation v. Braun; Irmisch; Nelles; Chemische Berichte; vol. 66; (1933); p. 1471,1474 View in Reaxys
nickel
P2O5 Rx-ID: 6674943 View in Reaxys 23/29
Yield
Conditions & References Hydrogenation, Kinetics Truffault; Bulletin de la Societe Chimique de France; vol. <5> 1; (1934); p. 391,400; Bulletin de la Societe Chimique de France; vol. <5> 3; (1936); p. 442,444 View in Reaxys
Cr2O3
nickel
P2O5
Rx-ID: 6674944 View in Reaxys 24/29 Yield
Conditions & References Hydrogenation, Kinetics Truffault; Bulletin de la Societe Chimique de France; vol. <5> 1; (1934); p. 391,400; Bulletin de la Societe Chimique de France; vol. <5> 3; (1936); p. 442,444 View in Reaxys
carbon disulfide solution
Cl
tetracyclohexyl-benzene Rx-ID: 7087719 View in Reaxys 25/29 Yield
Conditions & References Hueckel; Bretschneider; Justus Liebigs Annalen der Chemie; vol. 540; (1939); p. 157,180 View in Reaxys
Cl
aluminium
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Rx-ID: 7044235 View in Reaxys 26/29 Yield
Conditions & References Turowa-Poljak; Dawydowa; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 2710,2713; engl. Ausg. S. 3019, 3021 View in Reaxys
Cl Al
Cl
HO
Cl
Rx-ID: 6677338 View in Reaxys 27/29 Yield
Conditions & References Zukerwanik; Ssidorowa; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 641,642; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 579 View in Reaxys
Cl Al
Cl
Cl
Rx-ID: 7407499 View in Reaxys 28/29 Yield
Conditions & References Nametkin; Pokrowsskaja; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 962,970; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 1569 View in Reaxys
Rx-ID: 7027008 View in Reaxys 29/29 Yield
Conditions & References p-Terphenyl , H2/Raney-Ni Patent; MTA Kozponti Fizikai Kutato Intezet; HU152087; (1965); ; vol. 63; nb. 5541b; (1965) View in Reaxys p-Terphenyl, Hochdruckhydrierung an Ni bei 200 - 275grad Scola et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 384,388 View in Reaxys p-Terphenyl, Hochdruckhydrierung an CuCrO4 bei 200 - 275grad Scola et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 384,388 View in Reaxys
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aus Benzol bei Hydrodimerisierung (durch IR, 1H-NMR identifiziert) Slaugh; Leonard; Journal of Catalysis; vol. 13; (1969); p. 385,395 View in Reaxys p-Terphenyl, H2, Raney-Ni, Cyclohexan, 150-160grad, 100-120 bar Bahurel et al.; Bulletin de la Societe Chimique de France; (1968); p. 4259 View in Reaxys Cyclohexanol, Benzol, H2SO4 Farberov et al.; Neftekhimiya; vol. 9; (1969); p. 107,114 View in Reaxys
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