Cyclopentanone by Asch

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Bioactivities (19670)

Yield

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Reactions (449)

Substances (1)

Targets (1116)

Citations (814)

Conditions

References A

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298

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A: 9% B: 1.5% C: 44% D: 3.5% E: 12%

With water; nitrogen(II) oxide

7.96667 h; Irradiationfurther reaction times, initial conc.,; Product distribution;

299

Takagi, H.; Washida, N.; Banbow, H.; Akimoto, H.; Okuda, M.

Journal of Physical Chemistry, 1981 , vol. 85, # 18 p. 2701 - 2705 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar Rx-ID: 2055578 Find similar reactions

A: 83.1 % Chromat. B: 0.5 % Chromat.

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With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; dihydrogen peroxide

1) THF, 65 deg C, 24 h; Product distribution;

Brown, Herbert C.; Chen, Jackson C.

Journal of Organic Chemistry, 1981 , vol. 46, # 20 p. 3978 - 3988 Title/Abstract Full Text View citing articles Show Details

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300

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A: 2 % Chromat. B: 82.2 % Chromat.

With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; dihydrogen peroxide

1) THF, 25 deg C, 1.5 h; Product distribution;

Brown, Herbert C.; Chen, Jackson C.

Journal of Organic Chemistry, 1981 , vol. 46, # 20 p. 3978 - 3988 Title/Abstract Full Text View citing articles Show Details

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301

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B: 91.6%

With hydrogenchloride; dihydrogen peroxide in acetonitrile

Rao, Darvasula V.; Stuber, Fred A.

T=50°C; 3 h; the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C;

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

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302

Synthesize Find similar Rx-ID: 2163692 Find similar reactions

A: 58 % Turnov. B: 22 % Turnov.

With sodium peroxodisulphate; silver nitrate in water

T=60°C; 3 h;

Ogibin, Yu. N.; Velibekova, D. S.; Katsin, M. I.; Troyanskii, E. I.; Nikishin, G. I.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1981 , vol. 30, # 12 p. 2293 - 2298 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1981 , # 12 p. 2755 - 2761 Title/Abstract Full Text View citing articles Show Details

303

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Rx-ID: 2200077 Find similar reactions

With sodium acetate (buffer) in acetic acid

Wistuba, Eckehardt; Ruechardt, Christoph

Tetrahedron Letters, 1981 , vol. 22, # 41 p. 4069 - 4072 Title/Abstract Full Text View citing articles Show Details

in acetic acid

rate constant: 171.4E5; Rate constant;

Wistuba, Eckehardt; Ruechardt, Christoph

Tetrahedron Letters, 1981 , vol. 22, # 41 p. 4069 - 4072 Title/Abstract Full Text View citing articles Show Details

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304

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Find similar

Rx-ID: 2537155 Find similar reactions

A: 70.3%

Find similar

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

With hydrogenchloride; dihydrogen peroxide in acetonitrile

T=50°C; 3 h; the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C;

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305

Synthesize Find similar Rx-ID: 2538740 Find similar reactions

A: 60%

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

With hydrogenchloride; dihydrogen peroxide in acetonitrile

T=50°C; 3 h; the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C;

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306

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Rx-ID: 3382729 Find similar reactions

With potassium hydroxide; Ru(O2CCF3)2(CO)(PPh3)2

T=140°C; ΔG (gas); Equilibrium constantThermodynamic data;

Strohmeier, Walter; Graser, Barbara

Zeitschrift fuer Physikalische Chemie (Muenchen, Germany), 1980 , vol. 121, p. 121 - 130 Title/Abstract Full Text Show Details

With potassium hydroxide; Ru(CF3CO2)CO(PPh3)2

T=140°C; 4 h; Equilibrium constant;

Graser, Barbara; Strohmeier, Walter; Marcec, Radovan; Steigerwald, Hannelore

Berichte der Bunsen-Gesellschaft, 1981 , vol. 85, # 7 p. 671 - 677 Title/Abstract Full Text Show Details

With potassium hydroxide; Ru(CF3CO2)CO(PPh3)2

T=140°C; 5 h; Equilibrium constantRate constant;

Graser, Barbara; Strohmeier, Walter; Marcec, Radovan; Steigerwald, Hannelore

Berichte der Bunsen-Gesellschaft, 1981 , vol. 85, # 7 p. 671 - 677 Title/Abstract Full Text Show Details

307

Synthesize Find similar Rx-ID: 3804869 Find similar reactions

A: 11.6 % Chromat. B: 7 % Chromat. C: 2.1 % Chromat. D: 46 % Chromat.

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Brown, Herbert C.; Chen, Jackson C.

Journal of Organic Chemistry, 1981 , vol. 46, # 20 p. 3978 - 3988 Title/Abstract Full Text View citing articles Show Details

With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; dihydrogen peroxide

1) CCl4, 25 deg C, 22 h; Product distribution;

308

Synthesize Find similar 85%

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Rx-ID: 3927606 Find similar reactions

With trimethylsilyl iodide in chloroform

Ambient temperatureor reflux;

Ho, Tse-Lok

Synthetic Communications, 1981 , vol. 11, # 2 p. 101 - 104 Title/Abstract Full Text Show Details

309

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Rx-ID: 21440830 Find similar reactions

Multi-step reaction with 2 steps 1: 90.6 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 2: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

310

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Rx-ID: 21440837 Find similar reactions

Multi-step reaction with 3 steps 1: 80 percent / 85percent phosphoric acid / 4 h / Ambient temperature 2: 100 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 3: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

Multi-step reaction with 3 steps 1: 80 percent / 85percent phosphoric acid / 4 h / Ambient temperature 2: 92 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 3: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

Multi-step reaction with 3 steps 1: 80 percent / 85percent phosphoric acid / 4 h / Ambient temperature 2: 90.6 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 3: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

311

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Rx-ID: 21448912 Find similar reactions

Multi-step reaction with 2 steps 1: 92 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 2: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

312

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

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Rx-ID: 21449231 Find similar reactions

Multi-step reaction with 2 steps 1: 100 percent / PdCl2(PhCN)2 / benzene / 2 h / Heating 2: 30percent H2O2, conc. HCl / acetonitrile / 3 h / 50 °C / the excess of H2O2 was removed by catalytic hydrogenation using 10percent Pd-C View Scheme

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

313

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314

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Rx-ID: 21469405 Find similar reactions

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

Rao, Darvasula V.; Stuber, Fred A.

Tetrahedron Letters, 1981 , vol. 22, # 25 p. 2337 - 2340 Title/Abstract Full Text View citing articles Show Details

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Rx-ID: 21477840 Find similar reactions

Multi-step reaction with 2 steps 1: pyridine / 2.5 h / 3 °C 2: acetic acid / rate constant: 171.4E5

View Scheme

Wistuba, Eckehardt; Ruechardt, Christoph

Tetrahedron Letters, 1981 , vol. 22, # 41 p. 4069 - 4072 Title/Abstract Full Text View citing articles Show Details

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315

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Rx-ID: 27050641 Find similar reactions

B: 26%

With 1-hydroxycyclopentane in 1,2-dichloro-ethane

byproducts: BF3-pyridine complex, H2O; under Ar addn. of BF3*Et2O to mixt. of alcohol and complex in (CH2)2Cl2, further addn. of BF3*Et2O, heating in 60°C oil bath for 60 min,addn. 1 drop of pyridine in hexane, removing BF3-pyridine complex pptd.; solvent removing in vac., addn. of petroleum ether to resulting oil, filtration, drying under Ar;

Tovrog,Benjamin S.; Diamond, Steven E.; Mares, Frank; Szalkiewicz, Andrew

Journal of the American Chemical Society, 1981 , vol. 103, # 12 p. 3522 - 3526 Title/Abstract Full Text View citing articles Show Details

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316

Synthesize Find similar Rx-ID: 1507151 Find similar reactions

Product distribution;

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Bauduin, G.; Bondon, D.; Pietrasanta, Y.; Pucci, B.

Tetrahedron, 1980 , vol. 36, # 2 p. 245 - 254 Title/Abstract Full Text View citing articles Show Details

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317

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Rx-ID: 1515129 Find similar reactions

Bauduin, G.; Bondon, D.; Pietrasanta, Y.; Pucci, B.

Tetrahedron, 1980 , vol. 36, # 2 p. 245 - 254 Title/Abstract Full Text View citing articles Show Details

Product distribution;

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318

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Rx-ID: 1581947 Find similar reactions

A: 3.3% B: 2.5% C: 1% D: 59.3%

Tomioka, Hideo; Okuno, Hiroshi; Izawa, Yasuji

Journal of Organic Chemistry, 1980 , vol. 45, # 26 p. 5278 - 5283 Title/Abstract Full Text View citing articles Show Details

in benzene

Irradiationaddition of methanol in the dark after irradiation, nondegassed solvent; Product distributionMechanism;

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319

Synthesize Find similar Rx-ID: 1976886 Find similar reactions

A: 9 % Chromat. B: 36 %

With oxygen

T=60°C; P=759.8 Torr;

Blau, K.; Mueller, U.; Pritzkow, W.; Schmidt-Renner, W.; Sedshaw, Z.

Journal fuer Praktische Chemie (Leipzig), 1980 , vol. 322, # 6 p. 915 - 932 Title/Abstract Full Text Show Details

Chromat. C: 41 % Chromat. D: 14 % Chromat.

A: 9 % Chromat. B: 36 % Chromat. C: 41 % Chromat. D: 14 % Chromat.

With oxygen

T=60°C; P=759.8 Torr; Title compound not separated from byproducts;

Blau, K.; Mueller, U.; Pritzkow, W.; Schmidt-Renner, W.; Sedshaw, Z.

Journal fuer Praktische Chemie (Leipzig), 1980 , vol. 322, # 6 p. 915 - 932 Title/Abstract Full Text Show Details

A: 9 % Chromat. B: 36 % Chromat. C: 41 % Chromat. D: 14 % Chromat.

With oxygen

T=60°C; P=759.8 Torr; Mechanism;

Blau, K.; Mueller, U.; Pritzkow, W.; Schmidt-Renner, W.; Sedshaw, Z.

Journal fuer Praktische Chemie (Leipzig), 1980 , vol. 322, # 6 p. 915 - 932 Title/Abstract Full Text Show Details

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320

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Rx-ID: 2340736 Find similar reactions

Paul, Mueller; Blanc, Jacky

Helvetica Chimica Acta, 1980 , vol. 63, # 7 p. 1759 - 1766 Title/Abstract Full Text Show Details

With aluminum isopropoxide in benzene

T=80°C; -ΔGox; Equilibrium constantThermodynamic data;

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321

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A: 5% B: 3% C: 43% D: 18%

in methanol

12 h; Irradiationphotolysis in presence of sensitizer, photolysis in methanol-d4 for 6 h; Product distributionMechanism;

Feld, W. A.; Serve, M. P.

Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 825 - 827 Title/Abstract Full Text Show Details

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322

Synthesize Find similar Rx-ID: 3063997 Find similar reactions

A: 5% B: 5% C: 9% D: 3% E: 43% F: 11%

Feld, W. A.; Serve, M. P.

Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 825 - 827 Title/Abstract Full Text Show Details

in cyclohexane

12 h; Irradiation; Product distributionMechanism;

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323

Synthesize Find similar Rx-ID: 3063999 Find similar reactions

A: 3% B: 47% C: 21%

Feld, W. A.; Serve, M. P.

Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 825 - 827 Title/Abstract Full Text Show Details

in acetonitrile

12 h; Irradiationphotolysis in presence of sensitizer; Product distributionMechanism;

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324

Synthesize Find similar Rx-ID: 3112338 Find similar reactions

in decane

T=0°C; Irradiation; Title compound not separated from byproducts;

Kopecky, Karl R.; Sastre, Juan A. Lopez

Canadian Journal of Chemistry, 1980 , vol. 58, # 19 p. 2089 - 2092 Title/Abstract Full Text Show Details

With 1,5-diphenyl-1,4-pentadiene-3-one in benzene

T=40.9°C; IrradiationEa, ΔS(excit.); KineticsThermodynamic dataProduct distribution;

Kopecky, Karl R.; Sastre, Juan A. Lopez

Canadian Journal of Chemistry, 1980 , vol. 58, # 19 p. 2089 - 2092 Title/Abstract Full Text Show Details

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325

Synthesize Find similar Rx-ID: 3125077 Find similar reactions

Fedyanin, N. P.

J. Appl. Chem. USSR (Engl. Transl.), 1980 , vol. 53, # 10 p. 2306 - 2309,1755 - 1758 Title/Abstract Full Text Show Details

T=320°C; presence of solvent; Rate constantMechanism;

326

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100%

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Rx-ID: 3172200 Find similar reactions

With hydrogenchloride

0.0416667 h; Ambient temperaturepH = 4-6, regeneration of aldehyde; Product distribution;

327

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Ohta, Shunsaku; Okamoto, Masao

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 6 p. 1917 - 1919 Title/Abstract Full Text Show Details

Find similar Rx-ID: 3345337 Find similar reactions

A: 42% B: 52%

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With sodium dithionite; sodium hydrogencarbonate in water

4 h; Heating;

de Vries, Johannes G.; Kellogg, Richard M.

Journal of Organic Chemistry, 1980 , vol. 45, # 21 p. 4126 - 4129 Title/Abstract Full Text View citing articles Show Details

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328

Synthesize Find similar Rx-ID: 3476364 Find similar reactions

With dimethylsulfide in methanol

dry ice-acetone to room temperature; Yields of byproduct given;

Wrobel, Jay; Cook, J. M.

Synthetic Communications, 1980 , vol. 10, # 4 p. 333 - 338 Title/Abstract Full Text Show Details

With dimethylsulfide in methanol

dry ice-acetone to room temperature; Yield given;

Wrobel, Jay; Cook, J. M.

Synthetic Communications, 1980 , vol. 10, # 4 p. 333 - 338 Title/Abstract Full Text Show Details

329

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33%

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Wakatsuki, Yasuo; Nomura, Okio; Tone, Hiroatsu; Yamazaki, Hiroshi

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1980 , p. 1344 - 1349 Title/Abstract Full Text View citing articles Show Details

in benzene

P=33097.9 Torr; 168 h; Ambient temperature;

330

Rx-ID: 5929731 Find similar reactions

Synthesize Find similar Rx-ID: 1072455 Find similar reactions

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Bigler,P.; Neuenschwander,M.

Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details

T=20°C; Equilibrium constant;

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331

Synthesize Find similar Rx-ID: 26756965 Find similar reactions

A: 72% C: 28%

byproducts: (C4H9)3SnCH(CH3)COOCH3, CO2; 60 percent decompn. at 180°C/5 Torr within 8 h;

Didier, P.; Pommier, J. C.

Journal of Organometallic Chemistry, 1978 , vol. 150, p. 203 - 214 Full Text View citing articles Show Details

A: 72% C: 28%

byproducts: (C4H9)3SnCH(CH3)COOCH3, CO2; 60 percent decompn. at 180°C/5 Torr within 8 h;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

A: 68% C: 32%

byproducts: (C4H9)3SnCH(CH3)COOCH3, CO2; 63 percent decompn. at 200°C/5 Torr within 5 h;

Didier, P.; Pommier, J. C.

Journal of Organometallic Chemistry, 1978 , vol. 150, p. 203 - 214 Full Text View citing articles Show Details

Hide Details

A: 68% C: 32%

332

byproducts: (C4H9)3SnCH(CH3)COOCH3, CO2; 63 percent decompn. at 200°C/5 Torr within 5 h;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

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Rx-ID: 26755221 Find similar reactions

With NO{BF4} in dichloromethane

Olah, G. A.; Ho, T. L.

Synthesis, 1976 , p. 609 - 610 Full Text Show Details

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

With NO{BF4} in dichloromethane

333

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Rx-ID: 952575 Find similar reactions

With perchloric acid

Jaeger,G.

Chemische Berichte, 1972 , vol. 105, p. 137 - 149 Full Text View citing articles Show Details

334

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Rx-ID: 26755726 Find similar reactions

88%

decompn. at 150°C for 0.5 h;

Delmond; Pommier

Tetrahedron Letters, 1968 , p. 6147 Full Text View citing articles Show Details

88%

decompn. at 150°C for 0.5 h;

Delmond, Bernard; Pommier, Jean-Claude; Valade, Jacques

Journal of Organometallic Chemistry, 1972 , vol. 35, # 1 p. 91 - 104

Title/Abstract Full Text View citing articles Show Details

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

335

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79%

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Rx-ID: 26755743 Find similar reactions

Delmond, Bernard; Pommier, Jean-Claude; Valade, Jacques

Journal of Organometallic Chemistry, 1972 , vol. 35, # 1 p. 91 - 104 Title/Abstract Full Text View citing articles Show Details

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

decompn. at 210°C for 0.5 h;

336

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Rx-ID: 1130981 Find similar reactions

Burgstahler,A.W. et al.

Journal of Organic Chemistry, 1966 , vol. 31, p. 3516 - 3522 Full Text View citing articles Show Details

(i) Pb(OAc)4, aq. AcOH, (ii) Pd-C, H2, HClO4, aq. EtOH; Multistep reaction;

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337

Synthesize Find similar Rx-ID: 5957084 Find similar reactions

T=110°C; P=152000 Torr;

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Lonza A.G.

Patent: US2851486 , 1956 ;

Full Text Show Details

Natta; Albanesi

Chimica e l'Industria (Milan, Italy), 1966 , vol. 48, p. 1157 Full Text View citing articles Show Details

338

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Rx-ID: 22532150 Find similar reactions

Multi-step reaction with 2 steps 1: H2 / Pd-C / aq. ethanol 2: (i) Pb(OAc)4, aq. AcOH, (ii) Pd-C, H2, HClO4, aq. EtOH View Scheme

Burgstahler,A.W. et al.

Journal of Organic Chemistry, 1966 , vol. 31, p. 3516 - 3522 Full Text View citing articles Show Details

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339

Synthesize Find similar Rx-ID: 1094069 Find similar reactions

With water

T=25 - 50°C; KineticsEquilibrium constant;

Fiarman,I.D.; Gettler,J.D.

Journal of the American Chemical Society, 1962 , vol. 84, p. 961 - 966 Full Text View citing articles Show Details

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340

Synthesize Find similar Rx-ID: 1111603 Find similar reactions

With water

T=25 - 50°C; KineticsEquilibrium constant;

Brooks,D.W.; Gettler,J.D.

Journal of Organic Chemistry, 1962 , vol. 27, p. 4469 - 4475 Full Text View citing articles Show Details

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341

Synthesize Find similar Rx-ID: 7062573 Find similar reactions

Landa et al.

Collection of Czechoslovak Chemical Communications, 1959 , vol. 24, p. 1036,1038,1039 Full Text View citing articles Show Details

T=300°C;

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342

Synthesize Find similar Rx-ID: 191032 Find similar reactions

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T=25°C; Equilibrium constant;

Wheeler; Zabicky

Canadian Journal of Chemistry, 1958 , vol. 36, p. 656 Full Text View citing articles Show Details

El-Abbady

Journal of Organic Chemistry, 1956 , vol. 21, p. 828 Full Text View citing articles Show Details

Equilibrium constant;

Prelog; Kobelt

Helvetica Chimica Acta, 1949 , vol. 32, p. 1187,1191 Full Text View citing articles Show Details

Ruzicka; Plattner; Wild

Helvetica Chimica Acta, 1945 , vol. 28, p. 613,615 Full Text Show Details

343

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Rx-ID: 5687610 Find similar reactions

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Bartlett et al.

Journal of the American Chemical Society, 1958 , vol. 80, p. 126,135 Full Text View citing articles Show Details

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344

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Rx-ID: 5687613 Find similar reactions

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Newman; Harper

Journal of the American Chemical Society, 1958 , vol. 80, p. 6350,6353 Full Text View citing articles Show Details

T=30°C; Equilibrium constant;

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345

Synthesize Find similar Rx-ID: 7918742 Find similar reactions

T=25°C; Equilibrium constant;

Wheeler; Mateos

Canadian Journal of Chemistry, 1958 , vol. 36, p. 712,713 Full Text View citing articles Show Details

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346

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Rx-ID: 5687611 Find similar reactions

House; Wasson

Journal of the American Chemical Society, 1957 , vol. 79, p. 1488,1490 Full Text View citing articles Show Details

347

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Rx-ID: 5929732 Find similar reactions

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Hawthorne

Journal of the American Chemical Society, 1957 , vol. 79, p. 2510,2512 Full Text View citing articles Show Details

T=0°C; Rate constant;

348

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Rx-ID: 7446072 Find similar reactions

T=50°C; Rate constant;

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Hawthorne; Strahm

Journal of the American Chemical Society, 1957 , vol. 79, p. 2515,2517 Full Text View citing articles Show Details

349

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Rx-ID: 7446073 Find similar reactions

Braude; Forbes

Journal of the Chemical Society, 1951 , p. 1755,1760 Full Text View citing articles Show Details

Goering et al.

Journal of the American Chemical Society, 1957 , vol. 79, p. 2502,2503 Full Text View citing articles Show Details

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350

Rx-ID: 5687608 Find similar reactions

With chloroform; sulfuric acid

Boyer et al.

Journal of the American Chemical Society, 1956 , vol. 78, p. 325 Full Text View citing articles Show Details

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351

Synthesize Find similar Rx-ID: 7446080 Find similar reactions

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Boyer et al.

Journal of the American Chemical Society, 1956 , vol. 78, p. 325 Full Text View citing articles Show Details

352

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Rx-ID: 256725 Find similar reactions

With hydrogen bromide

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

353

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Rx-ID: 258935 Find similar reactions

With hydrogen bromide

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

Multi-step reaction with 2 steps 1: aqueous KOH-solution 2: HBr View Scheme

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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354

Synthesize Find similar Rx-ID: 315591 Find similar reactions

With dichloromethane; ozone

T=-80°C;

Criegee et al.

Justus Liebigs Annalen der Chemie, 1953 , vol. 583, p. 1,28 Full Text View citing articles Show Details

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355

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Rx-ID: 7061520 Find similar reactions

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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356

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Rx-ID: 7061521 Find similar reactions

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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357

Synthesize Find similar Rx-ID: 7061522 Find similar reactions

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Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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358

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Rx-ID: 7061523 Find similar reactions

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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359

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Rx-ID: 7061524 Find similar reactions

Crombie; Hancock; Linstead

Journal of the Chemical Society, 1953 , p. 3502 Full Text View citing articles Show Details

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360

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Criegee et al.

Justus Liebigs Annalen der Chemie, 1953 , vol. 583, p. 1,28 Full Text View citing articles Show Details

T=-80°C;

361

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Rx-ID: 7061513 Find similar reactions

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Bridson-Jones et al.

Journal of the Chemical Society, 1951 , p. 2999,3006 Full Text View citing articles Show Details

T=300°C; P=330978 Torr;

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362

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Rx-ID: 7061528 Find similar reactions

Poggi; Serchi

Gazzetta Chimica Italiana, 1950 , vol. 80, p. 385 Full Text View citing articles Show Details

T=0°C; und 18grad; Equilibrium constant;

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363

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Mousseron; Jacquier

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1949 , vol. 229, p. 216 Bulletin de la Societe Chimique de France, 1950 , p. 238,243 Full Text View citing articles Show Details

364

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Rx-ID: 5687607 Find similar reactions

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Mousseron; Jullien; Winternitz

Bulletin de la Societe Chimique de France, 1948 , p. 878,885 Full Text View citing articles Show Details

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365

Synthesize Find similar Rx-ID: 5727121 Find similar reactions

Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

T=200 - 300°C;

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366

Synthesize Find similar Rx-ID: 5727122

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Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

T=200 - 300°C;

367

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Rx-ID: 5929729 Find similar reactions

With nickel-copper catalyst; hydrogen

Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

With hydrogen; nickel

Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

With cobalt-copper catalyst; hydrogen

Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

Hide Details

With cobalt catalyst; nitrogen

T=250 - 300°C;

Wilson

Journal of the American Chemical Society, 1948 , vol. 70, p. 1313 Full Text View citing articles Show Details

368

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Rx-ID: 6682680 Find similar reactions

Nesmejanow; Petscherskaja; Urezkaja

Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1948 , p. 240,243 Chem.Abstr., 1948 , p. 4924 Full Text View citing articles Show Details

T=250 - 280°C;

369

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Rx-ID: 7061529 Find similar reactions

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Hauser; Swamer; Ringler

Journal of the American Chemical Society, 1948 , vol. 70, p. 4023,4025 Full Text View citing articles Show Details

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370

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Phillips Petr. Co.

Patent: US2452741 , 1947 ;

T=140°C; P=20594.2 Torr;

Full Text Show Details

371

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T=150 - 275°C; Equilibrium constant;

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Rx-ID: 7076710 Find similar reactions

Cubberley; Mueller

Journal of the American Chemical Society, 1946 , vol. 68, p. 1150 Full Text View citing articles Show Details

372

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Rx-ID: 8258081 Find similar reactions

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Mousseron et al.

Bulletin de la Societe Chimique de France, 1946 , p. 629,632 Full Text View citing articles Show Details

T=50°C; Geschwindigkeit.Hydrolysis;

373

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Rx-ID: 5929736 Find similar reactions

With iron; zinc

T=425°C;

I.G. Farbenind.

Patent: DE743004 , 1940 ;

With zinc/copper couple

T=450°C;

Phillips Petr. Co.

Patent: US2377412 , 1944 ;

Full Text Show Details

I.G. Farbenind.

Patent: DE765200 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details

374

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Rx-ID: 7061514 Find similar reactions

T=450°C; Ueberleiten des Dampfes;

I.G. Farbenind.

Patent: DE765200 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details

T=290 - 340°C; Ueberleiten des Dampfes;

Phillips Petr. Co.

Patent: US2377412 , 1944 ; Full Text Show Details

375

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Rx-ID: 7061517 Find similar reactions

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Shell Devel. Co.

Patent: US2391740 , 1944 ;

T=185°C;

Full Text Show Details

376

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With potassium permanganate; sulfuric acid

With sulfuric acid; lead dioxide

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Rx-ID: 120750 Find similar reactions

Buchman; Sargent

Journal of Organic Chemistry, 1942 , vol. 7, p. 140,145 Full Text View citing articles Show Details

Wallach

Justus Liebigs Annalen der Chemie, 1918 , vol. 414, p. 311 Justus Liebigs Annalen der Chemie, 1924 , vol. 437, p. 174 Full Text View citing articles Show Details

377

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Rx-ID: 596247 Find similar reactions

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With aluminium oxide catalyst; chromium

T=160 - 250°C; P=3677.5 Torr;

Phillips Petr. Co.

Patent: US2371794 , 1942 ; Full Text Show Details

With copper-nickel catalyst

T=160 - 250°C; P=3677.5 Torr;

Phillips Petr. Co.

Patent: US2371794 , 1942 ; Full Text Show Details

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378

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Rx-ID: 5687612 Find similar reactions

Hudson; Robinson

Journal of the Chemical Society, 1942 , p. 691 Full Text Show Details

Erhitzen des Reaktionsprodukts mit wss.-aethanol. Natronlauge;

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379

Synthesize Find similar Rx-ID: 7918743

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Mannich

Chemische Berichte, 1941 , vol. 74, p. 565,568 Full Text View citing articles Show Details

und Ansaeuern des Reaktionsgemisches mit wss.H2SO4;

380

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Rx-ID: 8258079 Find similar reactions

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Clutterbuck et al.

Biochemical Journal, 1940 , vol. 34, p. 664,666, 672 Full Text View citing articles Show Details

Hydrogenation;

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381

Synthesize Find similar Rx-ID: 102822 Find similar reactions

Neunhoeffer; Paschke

Chemische Berichte, 1939 , vol. 72, p. 919,927 Full Text View citing articles Show Details

Bei der thermischen Zersetzung des Bariumsalzes;

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382

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Rx-ID: 316613 Find similar reactions

Neunhoeffer; Paschke

Chemische Berichte, 1939 , vol. 72, p. 919,927 Full Text View citing articles Show Details

T=190°C;

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383

Rx-ID: 5929743 Find similar reactions

With ammonia; thorium(IV) dioxide

T=350°C;

I.G. Farbenind.

Patent: DE743967 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details

With aluminum oxide; ammonia

T=350°C;

I.G. Farbenind.

Patent: DE743967 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details

384

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Rx-ID: 302593 Find similar reactions

With sulfuric acid

T=130 - 135°C;

Wenus-Danilowa

Zhurnal Obshchei Khimii, 1938 , vol. 8, p. 1179,1188 Chem. Zentralbl., 1940 , vol. 111, # I p. 1490 Full Text Show Details

With ethanol; mercury dichloride

T=100°C;

Wenus-Danilowa

Zhurnal Obshchei Khimii, 1938 , vol. 8, p. 1179,1188 Chem. Zentralbl., 1940 , vol. 111, # I p. 1490 Full Text Show Details

385

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Cornubert et al.

Bulletin de la Societe Chimique de France, 1938 , vol. <5> 5, p. 1490,1500 Bulletin de la Societe Chimique de France, 1939 , vol. <5> 6, p. 132,132 Anm. 3 Full Text View citing articles Show Details

T=165 - 220°C;

386

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Rx-ID: 7446071 Find similar reactions

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Wenus-Danilowa

Zhurnal Obshchei Khimii, 1938 , vol. 8, p. 1179,1188 Chem. Zentralbl., 1940 , vol. 111, # I p. 1490 Full Text Show Details

T=135°C;

387

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Rx-ID: 7446075 Find similar reactions

T=100°C;

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Wenus-Danilowa

Zhurnal Obshchei Khimii, 1938 , vol. 8, p. 1179,1188 Chem. Zentralbl., 1940 , vol. 111, # I p. 1490 Full Text Show Details

388

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Rx-ID: 523152 Find similar reactions

With sulfuric acid

Guha; Seshadriengar

Chemische Berichte, 1936 , vol. 69, p. 1212,1216 Full Text View citing articles Show Details

389

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Rx-ID: 5929737 Find similar reactions

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Demjanow; Schuikina

Zhurnal Obshchei Khimii, 1936 , vol. 6, p. 350 Chem. Zentralbl., 1936 , vol. 107, # II p. 1905 Full Text View citing articles Show Details

390

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Rx-ID: 5929738 Find similar reactions

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Demjanow; Schuikina

Zhurnal Obshchei Khimii, 1936 , vol. 6, p. 350 Chem. Zentralbl., 1936 , vol. 107, # II p. 1905 Full Text View citing articles Show Details

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391

Synthesize Find similar Rx-ID: 7061530 Find similar reactions

Kuhn; Koehler; Koehler

Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1936 , vol. 242, p. 186 Full Text View citing articles Show Details

T=-10°C;

392

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Rx-ID: 8258077 Find similar reactions

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Guha; Seshadriengar

Chemische Berichte, 1936 , vol. 69, p. 1212,1216 Full Text View citing articles Show Details

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393

Synthesize Find similar Rx-ID: 102823 Find similar reactions

T=313 - 320°C;

Vogel

Journal of the Chemical Society, 1929 , p. 732 Full Text View citing articles Show Details

T=315 - 320°C;

Vogel

Journal of the Chemical Society, 1929 , p. 732 Full Text View citing articles Show Details

CO2-Strom;

Aschan

Chemische Berichte, 1912 , vol. 45, p. 1605 Justus Liebigs Annalen der Chemie, 1911 , vol. 383, p. 58 Full Text View citing articles Show Details

394

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Rx-ID: 7446077 Find similar reactions

Kandiah; Linstead

Journal of the Chemical Society, 1929 , p. 2148 Full Text View citing articles Show Details

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395

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Rx-ID: 211639 Find similar reactions

Jupp; Kon; Lockton

Journal of the Chemical Society, 1928 , p. 1642 Full Text View citing articles Show Details

bei der Ozonspaltung;

396

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Find similar Rx-ID: 5687605 Find similar reactions

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9-<1-cyano-cyclopentyl>-'cis'-1.2.3.4.10.11-hexahydro-carbazole;

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Plant; Rippon

Journal of the Chemical Society, 1928 , p. 1907 Anm. Full Text View citing articles Show Details