Reaxys
PubChem
eMolecules
Reactions (526)
Yield
Substances (1)
Citations (573)
Conditions
References
298
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Rx-ID: 1642133 Find similar reactions
Nichols, Peter J.; Grant, Michael W.
Australian Journal of Chemistry, 1982 , vol. 35, # 12 p. 2455 - 2463 Title/Abstract Full Text Show Details
With strong acid; sodium perchlorate in water
T=25°C; Rate constant;
A
299
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B
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Rx-ID: 1783872 Find similar reactions
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Bamkole, Titus O.; Hirst, Jack; Onyido, Ikenna
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 889 - 894 Title/Abstract Full Text Show Details
in benzene
other solvent; Equilibrium constant;
A
B
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300
Synthesize Find similar Rx-ID: 2615947 Find similar reactions
Alberola, A.; Gonzalez, A. M.; Guerra, D.; Pulido, F. J.
Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 1073 - 1076 Title/Abstract Full Text Show Details
Heatingdecomposition in the mass spectrophotometer; Product distribution;
A
B
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301
Synthesize Find similar Rx-ID: 2618804 Find similar reactions
Alberola, A.; Gonzalez, A. M.; Guerra, D.; Pulido, F. J.
Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 1073 - 1076 Title/Abstract Full Text Show Details
Heatingdecomposition in the mass spectrophotometer; Product distribution;
A
302
B
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With water in dimethyl sulfoxide
Equilibrium constant;
Rossi, Rita H. de; Nunez, Alberto
Journal of Organic Chemistry, 1982 , vol. 47, # 2 p. 319 - 325 Title/Abstract Full Text View citing articles Show Details
A
B
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303
Synthesize Find similar Rx-ID: 2663596 Find similar reactions
With water in propan-1-ol
T=25°C; Rate constant;
Novikov, V. N.; Borodaev, S. V.; Babeshkina, L. D.
Chemistry of Heterocyclic Compounds (New York, NY, United States), 1982 , p. 448 - 454 Khimiya Geterotsiklicheskikh Soedinenii, 1982 , vol. 18, # 5 p. 601 - 609 Title/Abstract Full Text View citing articles Show Details
A
B
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304
Synthesize Find similar Rx-ID: 3000474 Find similar reactions
With tetrahydropyridine hydrochloride in dimethyl sulfoxide
T=25°C; Equilibrium constant;
Brooke, David N.; Crampton, Michael R.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 231 - 238 Title/Abstract Full Text Show Details
A
305
B
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With tetrahydropyridine hydrochloride in dimethyl sulfoxide
T=25°C; Equilibrium constant;
Brooke, David N.; Crampton, Michael R.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 231 - 238 Title/Abstract Full Text Show Details
A
B
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306
Synthesize Find similar Rx-ID: 4095096 Find similar reactions
Muralikrishna, U; Krishnamurthy, Mannam
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details
in chloroform
Equilibrium constant;
A
B
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307
Synthesize Find similar Rx-ID: 4095099 Find similar reactions
in chloroform
Equilibrium constant;
Muralikrishna, U; Krishnamurthy, Mannam
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details
A
B
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308
Synthesize Find similar Rx-ID: 4111959 Find similar reactions
Muralikrishna, U; Krishnamurthy, Mannam
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details
in chloroform
Equilibrium constant;
A
B
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309
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Rx-ID: 1783870 Find similar reactions
Ellenberger, Mark R.; Dixon, David A.; Farneth, William E.
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5377 - 5382 Title/Abstract Full Text View citing articles Show Details
ICR double resonance, proton affinity;
A
B
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310
Synthesize Find similar Rx-ID: 1783871 Find similar reactions
ICR double resonance, proton affinity;
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Ellenberger, Mark R.; Dixon, David A.; Farneth, William E.
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5377 - 5382 Title/Abstract Full Text View citing articles Show Details
A
B
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311
Synthesize Find similar Rx-ID: 1838015 Find similar reactions
With water
Eicher, Thoephil; Franke, Guenter
Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details
A
B
C
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312
Synthesize Find similar Rx-ID: 2038682 Find similar reactions
With sulfuric acid; chloramine-T in water; acetic acid
0.25 h; Ambient temperaturequantitative determination of the title compound; Product distribution;
Yusuff, K. K. M.; Gopalan, M.
Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1981 , vol. 20, # 8 p. 859 Title/Abstract Full Text Show Details
A
B
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313
Synthesize Find similar Rx-ID: 3002701 Find similar reactions
in dimethyl sulfoxide
T=25°C; kinetic of reactions of cyclic secondary amines (pyrrolidine, piperidine) with 2,4-dinitro-1-naphthyl ethyl ether in DMSO; stage I kinetics and equilibrium (with piperidine); Rate constantEquilibrium constantMechanism;
Bunnett, Joseph F.; Sekiguchi, Shizen; Smith, Lewis A.
Journal of the American Chemical Society, 1981 , vol. 103, # 16 p. 4865 - 4871 Title/Abstract Full Text View citing articles Show Details
A
B
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314
Synthesize Find similar Rx-ID: 3007370 Find similar reactions
With tetrahydropyridine hydrochloride in dimethyl sulfoxide
T=25°C; reversible reactions of amines with the corresponding N-(2,4-dinitro-1-naphthylamines); difference between pyrrolidine and piperidine systems; Equilibrium constantMechanism;
Sekiguchi, Shizen; Bunnett, J. F.
Journal of the American Chemical Society, 1981 , vol. 103, # 16 p. 4871 - 4874 Title/Abstract Full Text View citing articles Show Details
315
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Rx-ID: 20625318 Find similar reactions
Multi-step reaction with 3 steps 1: 69 percent / toluene 2: 81 percent / H2O of air / 2160 h 3: H2O View Scheme
Eicher, Thoephil; Franke, Guenter
Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details
316
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Multi-step reaction with 2 steps 1: 81 percent / H2O of air / 2160 h 2: H2O View Scheme
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Rx-ID: 20636184 Find similar reactions
Eicher, Thoephil; Franke, Guenter
Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details
A
B
C
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317
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Rx-ID: 1500319 Find similar reactions
A: 20% B: 15% C: 50%
With Ps(acac)2; triethylaluminum; triphenylphosphine in toluene
6 h; Heating;
Dzhemilev, U. M.; Selimov, F. A.; Tolstikov, G. A.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1980 , vol. 29, # 2 p. 263 - 266 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1980 , # 2 p. 348 - 352 Title/Abstract Full Text View citing articles Show Details
A
B
C
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318
Synthesize Find similar Rx-ID: 1500324 Find similar reactions
A: 50% B: 20%
With bis(acetylacetonato) palladium; triethylaluminum; triphenylphosphine in toluene
T=100°C; 4 h;
Dzhemilev, U. M.; Selimov, F. A.; Tolstikov, G. A.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1980 , vol. 29, # 2 p. 263 - 266 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1980 , # 2 p. 348 - 352 Title/Abstract Full Text View citing articles Show Details
A
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C
D
E
F
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319
Synthesize Find similar Rx-ID: 1513436 Find similar reactions
With hydrogen; sulphidized CoO-MoO3
T=300°C; P=37503 Torr; 1 h; prolonged (9 h) heating affords additional N-(1-butyl)piperidine, N-(1-ethyl)piperidine, and decane; MechanismProduct distribution;
Cerny, Mirko
Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 8 p. 2215 - 2218 Title/Abstract Full Text Show Details
A
B
C
D
E
F
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320
Synthesize Find similar Rx-ID: 1516278 Find similar reactions
A: 5.4% B: 5.8% C: 0.8% D: 3%
With hydrogen; sulphidized CoO-MoO3
T=300°C; P=45003.6 - 90757.2 Torr; 8 h; MechanismProduct distribution;
Cerny, Mirko
Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 8 p. 2215 - 2218 Title/Abstract Full Text Show Details
A
B
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321
Synthesize Find similar Rx-ID: 1723878 Find similar reactions
With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
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322
Synthesize Find similar Rx-ID: 1723879 Find similar reactions
With formic acid in various solvent(s)
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
T=0°C; var. solvents; Rate constant;
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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323
Synthesize Find similar Rx-ID: 1725995 Find similar reactions
With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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324
Synthesize Find similar Rx-ID: 1774389 Find similar reactions
With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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325
Synthesize Find similar Rx-ID: 1775026 Find similar reactions
With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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326
Synthesize Find similar Rx-ID: 2331426 Find similar reactions
With formic acid in toluene
T=0°C; var. solvents and reagent ratio,; Rate constantMechanism;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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327
Synthesize Find similar Rx-ID: 3137712 Find similar reactions
With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;
Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru
Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details
A
B
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328
Synthesize Find similar Rx-ID: 3286599 Find similar reactions
Falk, Heinz; Mueller, Norbert; Schlederer, Thomas
Monatshefte fuer Chemie, 1980 , vol. 111, p. 159 - 176 Title/Abstract Full Text View citing articles Show Details
in dimethyl sulfoxide
T=22°C; temperature-dependence and solvent-dependence of the equilibrium; Equilibrium constant;
A
B
C
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329
Synthesize Find similar Rx-ID: 3953759 Find similar reactions
With water
T=37°C; Rate constant;
Bundgaard; Johansen
Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details
A
B
C
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330
Synthesize Find similar Rx-ID: 3953781 Find similar reactions
With water
T=37°C; Rate constant;
Bundgaard; Johansen
Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details
A
B
C
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331
Synthesize Find similar Rx-ID: 3974703 Find similar reactions
With water
T=37°C; Rate constant;
Bundgaard; Johansen
Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details
A
B
C
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332
Synthesize Find similar Rx-ID: 4019439 Find similar reactions
With water
T=37°C; Rate constant;
Bundgaard; Johansen
Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
E
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333
Synthesize Find similar Rx-ID: 4247669 Find similar reactions
With Fe2(CO)9 in benzene
T=45°C; 2 h; var. reaction partners and times; other N-alkyloxyamines; Product distributionMechanism;
A
B
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334
Rx-ID: 25355180 Find similar reactions
Blum, Y.; Becker, Y.; Shvo, Y.
Journal of Organometallic Chemistry, 1980 , vol. 202, # 1 p. 65 - 76 Title/Abstract Full Text View citing articles Show Details
E. I. Du Pont de Nemours and Company
Patent: US4220608 A1, 1980 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
9:HF and Piperidine
HF and Piperidine The procedure of Example 4 was repeated, using 12.8 g (0.15 mole) of piperidine in place of quinoline, and gave 1.5 g of 3,3,3-trifluoropropene-1. A
B
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335
Rx-ID: 25283140 Find similar reactions
Gruppo Lepetit S.p.A.
Patent: US4129562 A1, 1978 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
5:4-desoxy-2'-(piperidino)carbonyl-thiazolo[5,4-c]rifamycin SV
EXAMPLE 5 4-desoxy-2'-(piperidino)carbonyl-thiazolo[5,4-c]rifamycin SV The compound of the title was prepared according to the procedure of Example 3 from the compound of Example 1 and piperidine (M.p. 175°-178° C. with decomposition). A
B
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336
A: 65%
Rx-ID: 25209957 Find similar reactions
Societa' Farmaceutici Italia S.p.A.
Patent: US4024224 A1, 1977 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
3:14-(N-piperidino)-daunomycin
EXAMPLE 3 14-(N-piperidino)-daunomycin By following the procedures described in Example 1, but using an equivalent amount of piperidine instead of morpholine, 14-(N-piperidino)-daunomycin monohydrochloride was obtained; E1.2 = 1.7; E1 cm.1percent = 192 at 495 nm. (yield = 65percent). A
B
337
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Rx-ID: 25209958 Find similar reactions
Boehringer Ingelheim GmbH
Patent: US4021551 A1, 1977 ;
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Title/Abstract Full Text Show Details
24:EXAMPLE 24
EXAMPLE 24 Using a procedure analogous to that described in Example 23, 78percent of theory of 3,6-bis-[(α-piperidino-butyryl)-amino]-acridine hemihydrate, m.p. 103°-106° C. (recrystallized from ethanol/water), was obtained from 3,6-bis-(α-chlorobutyryl-amino)-acridine and piperidine. A
B
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338
Synthesize Find similar Rx-ID: 25282730 Find similar reactions
Boehringer Ingelheim GmbH
Patent: US4021551 A1, 1977 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
19:EXAMPLE 19
EXAMPLE 19 Using a procedure analogous to that described in Example 18, 68percent of theory of 3,6-bis-[α-(piperidino)-propionyl-amino]-acridine hydrate, m.p. 197°-201° C. (recrystallized from ethanol), was obtained from 3,6-bis-(α-chloropropionyl-amino)-acridine and piperidine. A
B
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339
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Rx-ID: 25282736 Find similar reactions
Boehringer Ingelheim GmbH
Patent: US4021551 A1, 1977 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
31:EXAMPLE 31
EXAMPLE 31 Using a procedure analogous to that described in Example 30, 70.9percent of theory of 3,6-bis-[(α-piperidino-isobutyryl)-amino]-acridine trihydrate, m.p. 131°-137° C. (recrystallized from ethanol), was obtained from 3,6-bis-(α-chloroisobutyryl-amino)-acridine and piperidine. A
B
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340
Rx-ID: 25209956 Find similar reactions
Richardson-Merrell Inc.
Patent: US3946021 A1, 1976 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
16:EXAMPLE 16
EXAMPLE 16 Following the procedure of Example 15, only substituting for dimethylaminie an excess amount of diethylamine and piperidine, the following compounds are prepared.
341
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Rx-ID: 25258804 Find similar reactions
With triethylamine
Mitsui Toatsu Chemicals, Incorporated
Patent: US3994932 A1, 1976 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
17:EXAMPLE 17
When the process was repeated using 60 grams of triethylamine or 52 grams of morpholine instead of the piperidine, similar results were obtained. A
B
342
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Rx-ID: 26730925 Find similar reactions
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Stynes; James
Journal of the American Chemical Society, 1974 , vol. 96, # 9 p. 2733 - 2738 Title/Abstract Full Text View citing articles Show Details
in toluene
Kinetics; 23°C;
Gmelin Handbook: Fe: Org.Verb.B1, 1.1.4.1.6.4.2.2, page 77 - 79 Full Text Show Details
A
B
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343
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Rx-ID: 90979 Find similar reactions
Zehrung; Woodburn
Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details
A
B
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344
Synthesize Find similar Rx-ID: 90981 Find similar reactions
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Zehrung; Woodburn
Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details
A
B
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345
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Rx-ID: 5404829 Find similar reactions
Ferles
Collection of Czechoslovak Chemical Communications, 1959 , vol. 24, p. 1029,1031, 1033 Full Text Show Details
bei der elektrochemischen Reduktion;
A
B
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346
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Rx-ID: 5411992 Find similar reactions
Zahradnik; Zuman
Collection of Czechoslovak Chemical Communications, 1959 , vol. 24, p. 1132,1136 Full Text Show Details
T=20 - 36°C; Zersetzung in gepufferten wss. Loesungen vom pH 4,1-5,8; Rate constant;
347
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Rx-ID: 8427187 Find similar reactions
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Zehrung; Woodburn
Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details
348
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Rx-ID: 5403481 Find similar reactions
Hales; Herington
Transactions of the Faraday Society, 1957 , vol. 53, p. 616,621 Full Text Show Details
T=140 - 260°C; Equilibrium constant;
349
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Rx-ID: 5742329 Find similar reactions
Schuikin; Tulupow
Vestnik Moskovskogo Universiteta, 1956 , vol. 11, # 3 p. 73,74 Chem.Abstr., 1956 , p. 12446 Full Text Show Details
T=150°C; Hydrogenation;
350
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Rx-ID: 222258 Find similar reactions
With kieselguhr; ammonia; cobalt
T=170°C; P=191232 Torr; Hydrogenation;
ICI
Patent: US2790804 , 1955 ;
With ammonia; nickel
ICI
Full Text Show Details
Patent: US2790804 , 1955 ;
T=170°C; P=147102 Torr; Hydrogenation;
Full Text Show Details
351
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Rx-ID: 5403465 Find similar reactions
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Reppe et al.
Justus Liebigs Annalen der Chemie, 1955 , vol. 596, p. 65 Full Text Show Details
T=310°C;
A
B
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352
Synthesize Find similar Rx-ID: 6799227 Find similar reactions
I.G. Farbenind.
Patent: DE765203 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details
Reppe et al.
Justus Liebigs Annalen der Chemie, 1955 , vol. 596, p. 162,182 Full Text Show Details
T=250°C;
A
B
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353
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Rx-ID: 824655 Find similar reactions
With sodium
T=165°C;
Terent'ew; Jaschunskii
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details
A
B
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354
Synthesize Find similar Rx-ID: 5497063 Find similar reactions
Kroehnke; Vogt
Justus Liebigs Annalen der Chemie, 1954 , vol. 589, p. 52 Full Text Show Details
A
B
C
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355
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Rx-ID: 7053304 Find similar reactions
Terent'ew; Jaschunskii
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details
A
B
C
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356
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Rx-ID: 7053305 Find similar reactions
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Terent'ew; Jaschunskii
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details
A
B
C
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357
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Rx-ID: 7053306 Find similar reactions
Terent'ew; Jaschunskii
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details
A
B
C
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358
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Rx-ID: 7053307 Find similar reactions
Terent'ew; Jaschunskii
Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details
A
359
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B
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Rx-ID: 5673491 Find similar reactions
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Micovic; Mihailovic
Journal of Organic Chemistry, 1953 , vol. 18, p. 1190,1196 Full Text Show Details
Mousseron et al.
Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details
T=-15°C; weniger als 1 Mol LiAlH4;
360
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Rx-ID: 166100 Find similar reactions
With sodium hydroxide; water
Bourns; Tudge
Canadian Journal of Chemistry, 1952 , vol. 30, p. 7371 Full Text Show Details
A
B
C
D
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361
Synthesize Find similar Rx-ID: 5418492 Find similar reactions
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T=400°C;
Malinowskii; Morgun
Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1952 , vol. 25, p. 333;engl.Ausg.S.367 Full Text View citing articles Show Details
T=450°C;
Malinowskii; Morgun
Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1952 , vol. 25, p. 333;engl.Ausg.S.367 Full Text View citing articles Show Details
A
B
362
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Rx-ID: 5469317 Find similar reactions
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Mousseron et al.
Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details
T=-15°C; weniger als 1 Mol LiAlH4;
A
B
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363
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Rx-ID: 5711573 Find similar reactions
Mousseron et al.
Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details
T=-15°C; weniger als 1 Mol LiAlH4;
A
B
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364
Synthesize Find similar Rx-ID: 5746102 Find similar reactions
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Kloosterziel et al.
Recueil des Travaux Chimiques des Pays-Bas, 1952 , vol. 71, p. 1231,1233 Full Text View citing articles Show Details
A
B
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365
Synthesize Find similar Rx-ID: 5408375 Find similar reactions
Sumitomo; Hachihama
Kogyo Kagaku Zasshi, 1951 , vol. 54, p. 199 Chem.Abstr., 1953 , p. 8060 Full Text Show Details
T=300 - 350°C; Hydrogenation;
A
B
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366
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Rx-ID: 5474881 Find similar reactions
Protiva; Jilek
Collection of Czechoslovak Chemical Communications, 1951 , vol. 16/17, p. 151 Full Text Show Details
A
B
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367
Synthesize Find similar Rx-ID: 5474882 Find similar reactions
T=130°C;
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Protiva; Jilek
Collection of Czechoslovak Chemical Communications, 1951 , vol. 16/17, p. 151 Full Text Show Details
368
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Rx-ID: 5685330 Find similar reactions
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Galinovsky et al.
Monatshefte fuer Chemie, 1951 , vol. 82, p. 551,557 Full Text Show Details
369
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Rx-ID: 5403478 Find similar reactions
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De Mayo; Rigby
Nature (London, United Kingdom), 1950 , vol. 166, p. 1075 Full Text View citing articles Show Details
A
B
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370
Synthesize Find similar Rx-ID: 222259 Find similar reactions
With ethanol; ammonia; nickel
T=110 - 150°C; P=58840.6 Torr; Hydrogenation;
Crum; Robinson
Journal of the Chemical Society, 1943 , p. 561,562
Full Text Show Details
With ammonia; cobalt
T=80 - 100°C; Hydrogenation;
I.G. Farbenind.
BIOS Final Rep. Nr. 350 <1946> Full Text Show Details
Reppe,W.
Acetylene Chemistry <New York 1949> S. 123 Full Text Show Details
Reppe
Experientia, 1949 , vol. 5, p. 93,108 Justus Liebigs Annalen der Chemie, 1953 , vol. 582, p. 1,16, 35 Full Text Show Details
371
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Rx-ID: 5403467 Find similar reactions
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Szmaragd; Briner
Helvetica Chimica Acta, 1949 , vol. 32, p. 553,560 Full Text Show Details
bei der elektrochemischen Reduktion;
372
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Rx-ID: 5403476 Find similar reactions
373
bei der elektrochemischen Reduktion;
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Szmaragd; Briner
Helvetica Chimica Acta, 1949 , vol. 32, p. 553,560 Full Text Show Details
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Rx-ID: 6798919 Find similar reactions
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Reppe,W.
Acetylene Chemistry <New York 1949> S. 98, 123 Full Text Show Details
Adkins; Cramer
Journal of the American Chemical Society, 1930 , vol. 52, p. 4349,4354 Full Text Show Details
Reppe
Experientia, 1949 , vol. 5, p. 93,108 Justus Liebigs Annalen der Chemie, 1953 , vol. 582, p. 1,16, 35 Full Text Show Details
T=110 - 150°C; P=58840.6 - 73550.8 Torr; Hydrogenation;
A
B
C
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374
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5704179 Find similar reactions
Schoepf et al.
Justus Liebigs Annalen der Chemie, 1948 , vol. 559, p. 1,22, 23 Chemische Berichte, 1951 , vol. 84, p. 690,698 Full Text Show Details
Hydrogenation;
375
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T=300°C;
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Rx-ID: 6798916 Find similar reactions
Scriabine
Bulletin de la Societe Chimique de France, 1947 , p. 454 Full Text Show Details
376
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Rx-ID: 5403464 Find similar reactions
With water; hydrogen bromide
Woods; Sanders
Journal of the American Chemical Society, 1946 , vol. 68, p. 2111 Full Text View citing articles Show Details
377
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Rx-ID: 6798914 Find similar reactions
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Woods; Sanders
Journal of the American Chemical Society, 1946 , vol. 68, p. 2111 Full Text View citing articles Show Details
A
B
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378
Synthesize Find similar Rx-ID: 5408376 Find similar reactions
T=140 - 215°C; P=102971 Torr; Hydrogenation;
Wilson
Journal of the American Chemical Society, 1945 , vol. 67, p. 693 Full Text View citing articles Show Details
379
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Rx-ID: 5403466 Find similar reactions
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Kline; Turkevich
Journal of the American Chemical Society, 1944 , vol. 66, p. 1710,1714 Full Text View citing articles Show Details
Jur'ew et al.
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 590,593 Chem. Zentralbl., 1940 , vol. 111, # II p. 902 Full Text Show Details
T=400 - 430°C;
A
B
C
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380
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5404665 Find similar reactions
Kline; Turkevich
Journal of the American Chemical Society, 1944 , vol. 66, p. 1710,1714 Full Text View citing articles Show Details
T=400°C;
A
B
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381
Synthesize Find similar Rx-ID: 19543 Find similar reactions
With kieselguhr; nickel
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Sawa et al.
T=200°C; P=55163.1 Torr; Hydrogenation;
Yakugaku Zasshi, 1943 , vol. 63, p. 319,324 Chem.Abstr., 1951 , p. 2940 Full Text Show Details
A
B
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382
Synthesize Find similar
Synthesize Find similar
Rx-ID: 22209 Find similar reactions
With kieselguhr; nickel
T=220°C; P=64724.7 Torr; Hydrogenation;
Sawa et al.
Yakugaku Zasshi, 1943 , vol. 63, p. 319,324 Chem.Abstr., 1951 , p. 2940 Full Text Show Details
A
B
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383
Synthesize Find similar
Synthesize Find similar
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Rx-ID: 288800 Find similar reactions
Dupont
Bulletin des Societes Chimiques Belges, 1942 , vol. 51, p. 209,220 Full Text Show Details
With piperidine; diethyl ether; xylene
anschliessend Behandeln mit HClO4;
384
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T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;
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Rx-ID: 5403468 Find similar reactions
Bergstrom; Carson
Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details
385
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Rx-ID: 5403479 Find similar reactions
Bergstrom; Carson
Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details
T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;
386
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Synthesize Find similar
Rx-ID: 5403487 Find similar reactions
Bergstrom; Carson
Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details
T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;
387
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Synthesize Find similar
Rx-ID: 5403488 Find similar reactions
Bergstrom; Carson
Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details
T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;
A
B
C
388
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Synthesize Find similar
Rx-ID: 5462953 Find similar reactions
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Mannich; Kniss
Chemische Berichte, 1941 , vol. 74, p. 1641 Full Text View citing articles Show Details
Anschliessend weitere Hydrierung an Palladium/Kohle in Aethanol..Hydrogenation;
389
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Synthesize Find similar
Rx-ID: 8274861 Find similar reactions
Mannich; Hoenig
Archiv der Pharmazie (Weinheim, Germany), 1927 , p. 601 Full Text Show Details
Dimroth; Resin; Zetzsch
Chemische Berichte, 1940 , vol. 73, p. 1399,1404 Full Text Show Details
T=170°C;
A
B
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390
Synthesize Find similar Rx-ID: 17377 Find similar reactions
With ammonia; hydrogen; nickel
T=450°C; P=22065.2 Torr;
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ; Full Text Show Details
391
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Rx-ID: 30376 Find similar reactions
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Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ;
With ammonia
T=150 - 250°C; P=147102 Torr; Hydrogenation.an einem Kobalt-Katalysator;
Full Text Show Details
I.G. Farbenind.
Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details
A
B
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392
Synthesize Find similar Rx-ID: 106801 Find similar reactions
With 1,4-dioxane; nickel
T=225°C; Hydrogenation;
D'Ianni; Adkins
Journal of the American Chemical Society, 1939 , vol. 61, p. 1675,1676 Full Text Show Details
393
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Synthesize Find similar
With ammonia
T=250°C; P=147102 Torr; Hydrogenation.an einen Kobalt-Katalysator;
Rx-ID: 161189 Find similar reactions
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ;
Full Text Show Details
I.G. Farbenind.
Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ;
With ammonia
T=280°C; P=169167 Torr; Hydrogenation.an einen Bariumoxid-Kupferoxid-Chromoxid-Katalysator;
Full Text Show Details
I.G. Farbenind.
Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details
394
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Rx-ID: 5403471 Find similar reactions
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Synthesize Find similar
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ;
T=150 - 250°C; P=147102 Torr; Hydrogenation;
Full Text Show Details
I.G. Farbenind.
Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details
395
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T=250°C; P=147102 Torr; Hydrogenation;
Synthesize Find similar
Rx-ID: 5403472 Find similar reactions
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ; Full Text Show Details
396
Synthesize Find similar T=280°C; P=169167 Torr; Hydrogenation;
Synthesize Find similar
Rx-ID: 5403473 Find similar reactions
Gen. Aniline and Film Corp.
Patent: US2265201 , 1939 ; Full Text Show Details