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Conditions
Citations (49)
References
1
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Rx-ID: 1040193 Find similar reactions
94%
With hydrogen in ethanol
T=60°C; P=15001.5 Torr; 0.333333 h; Autoclave; chemoselective reaction;
Ren, Yujing; Wei, Haisheng; Yin, Guangzhao; Zhang, Leilei; Wang, Aiqin; Zhang, Tao
Chemical Communications, 2017 , vol. 53, # 12 p. 1969 - 1972 Title/Abstract Full Text View citing articles Show Details
91%
With sulfuric acid in water; isopropyl alcohol
T=10 - 15°C; electrolysis;
Wessling, Michael; Schaefer, Hans J.
Chemische Berichte, 1991 , vol. 124, # 10 p. 2303 - 2306 Title/Abstract Full Text Show Details
82%
With sodium stannite in tetrahydrofuran; water
0.416667 h; Ambient temperature;
Varma, Rajender S.; Varma, Manju; Kabalka, George W.
Tetrahedron Letters, 1985 , vol. 26, # 49 p. 6013 - 6014 Title/Abstract Full Text View citing articles Show Details
81%
With zinc(II) tetrahydroborate in DME
6 h; Ambient temperature;
Ranu, Brindaban C.; Chakraborty, Rupak
Tetrahedron Letters, 1991 , vol. 32, # 29 p. 3579 - 3582 Title/Abstract Full Text View citing articles Show Details
81%
With zinc(II) tetrahydroborate in DME
T=25°C; 6 h;
Ranu; Chakraborty
Tetrahedron, 1992 , vol. 48, # 25 p. 5317 - 5322 Title/Abstract Full Text View citing articles Show Details
81%
With zinc(II) tetrahydroborate in DME
6 h; Ambient temperatureother α-substituted nitroalkenes;
Ranu, Brindaban C.; Chakraborty, Rupak
Tetrahedron Letters, 1991 , vol. 32, # 29 p. 3579 - 3582 Title/Abstract Full Text View citing articles Show Details
81%
With zinc(II) tetrahydroborate in DME
T=25°C; 6 h; other disubstituted nitroalkenes; Mechanism;
Ranu; Chakraborty
Tetrahedron, 1992 , vol. 48, # 25 p. 5317 - 5322 Title/Abstract Full Text View citing articles Show Details
67%
With sodium hypophosphite; palladium on activated charcoal in tetrahydrofuran
3 h; Ambient temperature;
Varma, Rajender S.; Varma, Manju; Kabalka, George W.
Synthetic Communications, 1986 , vol. 16, # 1 p. 91 - 96 Title/Abstract Full Text Show Details
With hydrogenchloride; tin(ll) chloride in methanol
T=-5°C;
Dornow,A.; Mueller,A.
Chemische Berichte, 1960 , vol. 93, p. 32 - 40 Full Text View citing articles Show Details
2
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Rx-ID: 780138 Find similar reactions
81%
With hydroxylamine hydrochloride; sodium carbonate in ethanol; water
24 h; Heating;
Langhals, Heinz; Range, Guenter; Wistuba, Eckehardt; Ruechardt, Christoph
Chemische Berichte, 1981 , vol. 114, # 12 p. 3813 - 3830 Title/Abstract Full Text Show Details
80%
With hydroxylamine hydrochloride; silica gel; tert-butanol
0.183333 h;
Kiasat, Ali Reza; Kazemi, Foad; Nourbakhsh, Kazem
Phosphorus, Sulfur and Silicon and the Related Elements, 2004 , vol. 179, # 6 p. 1193 - 1196 Title/Abstract Full Text View citing articles Show Details
80%
With Zincite; hydroxylamine hydrochloride; silica gel in neat (no solvent) T=20°C; 0.05 h; Green chemistry; Hide Experimental Procedure
Kiasat, Ali Reza; Javaherian, Mohammad; Daei, Mina; Farbod, Mansoor
Revue Roumaine de Chimie, 2015 , vol. 60, # 9 p. 875 - 880 Title/Abstract Full Text View citing articles Show Details
2. General procedure for preparation of oximes from aldehydes and ketones in the presence of ZnO nanotubes under solvent free condition General procedure: Hydroxylamine hydrochloride (0.138 g, 2 mmol), ZnO nanotubes (0.071 g, 0.8 mmol), silica gel (0.43 g) and aldehyde (ketone) (1 mmol) were ground together in a mortar with a pestle at room temperature for a period of time as indicated in Tables 1 and 2. The progress of the reaction was monitored by TLC. After complete disappearance of the starting materials, the reaction mixture was poured with diethyl ether (2×10 mL) and filtered to remove silica gel and ZnO nanotubes, The filtrate mixed with water and extracted. The solvent was removed in vaccuo to give the product which was recrystallized from suitable solvent and afforded the TLC and 1H-NMR pure products in 75-98 percent isolated yields.
47%
With hydroxylamine hydrochloride; sodium acetate in ethanol
T=20°C; 4 h;
Portela-Cubillo, Fernando; Lymer, James; Scanlan, Eoin M.; Scott, Jackie S.; Walton, John C.
Tetrahedron, 2008 , vol. 64, # 52 p. 11908 - 11916 Title/Abstract Full Text View citing articles Show Details
18%
With hydroxylamine hydrochloride; sodium hydroxide in ethanol; water
1 h; Reflux;
Yamamoto, Yutaro; Hasegawa, Hiroto; Yamataka, Hiroshi
Journal of Organic Chemistry, 2011 , vol. 76, # 11 p. 4652 - 4660 Title/Abstract Full Text View citing articles Show Details
With ethanol; hydroxylamine hydrochloride; sodium carbonate
Kolb
Justus Liebigs Annalen der Chemie, 1896 , vol. 291, p. 267 Full Text View citing articles Show Details
Dollfus
Chemische Berichte, 1892 , vol. 25, p. 1918 Chemische Berichte, 1893 , vol. 26, p. 1971 Full Text View citing articles Show Details
With ethanol; hydroxylamine hydrochloride; water; sodium acetate
Neber; v. Friedolsheim
Justus Liebigs Annalen der Chemie, 1926 , vol. 449, p. 129 Full Text View citing articles Show Details
With sodium hydroxide; hydroxylamine hydrochloride
Hey
Journal of the Chemical Society, 1930 , p. 18,20 Full Text View citing articles Show Details
With sodium hydroxide; hydroxylamine in water
0.25 h; Yield given;
Lozynski, Marek; Rusinska-Roszak, Danuta
Polish Journal of Chemistry, 1986 , vol. 60, # 4-6 p. 625 - 630 Title/Abstract Full Text Show Details
With pyridine; hydroxylamine hydrochloride in ethanol
Condensation; Heating;
Katritzky, Alan R.; Cui, Xilin; Long, Qiuhe; Yang, Baozhen; Wilcox, Allan L.; Zhang, Yong-Kang
Organic Preparations and Procedures International, 2000 , vol. 32, # 2 p. 175 - 183 Title/Abstract Full Text View citing articles Show Details
With hydroxylamine hydrochloride; sodium acetate in methanol; water
T=20°C;
Xuan, Jun; Xia, Xu-Dong; Zeng, Ting-Ting; Feng, Zhu-Jia; Chen, Jia-Rong; Lu, Liang-Qiu; Xiao, Wen-Jing
Angewandte Chemie - International Edition, 2014 , vol. 53, # 22 p. 5653 - 5656 Angew. Chem., 2014 , vol. 126, # 22 p. 5759 - 5762,4 Title/Abstract Full Text View citing articles Show Details
A
B
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3
Synthesize Find similar Rx-ID: 41124386 Find similar reactions
Multi-step reaction with 2 steps 1: N-butylamine / ethanol / |Reflux 2: acetic acid; tetraethylammonium tetrafluoroborate / DMFA; water / 20 °C / |Electrolysis View Scheme
A
4
Wessling, Michael; Schäfer, Hans J.
Beilstein Journal of Organic Chemistry, 2015 , vol. 11, p. 1163 - 1174 Title/Abstract Full Text View citing articles Show Details
B
Synthesize Find similar Rx-ID: 41124393 Find similar reactions
A: 20% B: 24%
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With tetraethylammonium tetrafluoroborate; acetic acid in water; DMFA
T=20°C; Electrolysis; Concentration; Hide Experimental Procedure
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Wessling, Michael; Schäfer, Hans J.
Beilstein Journal of Organic Chemistry, 2015 , vol. 11, p. 1163 - 1174 Title/Abstract Full Text View citing articles Show Details
Electrolyses
General procedure: The cathodic hydrodimerization is performed based on the results of the experiments shown in Tables 1 and 2 (Theoretical part) in an undivided cell (Figure 1a without diaphragm) at a mercury pool cathode at T = 0 °C (outside cooling). Electrolyte was a 0.2 M solution of tetraethylammonium p-toluenesulfonate (TEA-pTos) in DMF. The supporting electrolyte contained 2 percent water, is hygroscopic and was not dried. DMF is also not dried. To remove free amines the solvent was purged for some time with dry nitrogen gas. The supporting electrolyte is purged before the electrolyis for 10 min with nitrogen to remove dissolved oxygen. The given amount of substrate dissolved in 20 mL supporting electrolyte is given into the cell. The Luggin capillary is filled with electrolyte and positioned close to the cathode. Subsequently the anode is placed in the cell with a distance of 1 cm to the mercury surface. It is secured that in spite of the small distance to the cathode stirring of the mercury pool (500 t/min) can be done without disturbances of the current flow. Under argon the solution of the olefin is electrolyzed at the given potential until the current has decreased to 1–10 mA (istart = 250–450 mA). During the reduction – especially when stirring is stopped – at the cathode a deep colouring of the solution being red, brown or violet depending on the olefin can be observed. It diffuses into the solution and is discoloured at the anode. In the course of the electrolysis this leads to the colouring of the electrolyte. A
B
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5
Synthesize Find similar Rx-ID: 1986968 Find similar reactions
With tin(ll) chloride in acetone
0.75 h; Ambient temperature; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Varma, Rajender S.; Varma, Manju; Gai, Yuan-Zhu; Kabalka, George W.
Heterocycles, 1986 , vol. 24, # 9 p. 2581 - 2586 Title/Abstract Full Text View citing articles Show Details
With chromium dichloride; hydrogenchloride in tetrahydrofuran
0.166667 h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Varma, Rajender S.; Varma, Manju; Kabalka, George W.
Synthetic Communications, 1985 , vol. 15, # 14 p. 1325 - 1332 Title/Abstract Full Text Show Details
With sodium hydrogencarbonate; tin(ll) chloride
1.) acetone, RT, 45 min, 2.) acetone, pH=8, 15 min; Yield given. Multistep reaction. Yields of byproduct given;
Varma, Rajender S.; Varma, Manju; Gai, Yuan-Zhu; Kabalka, George W.
Heterocycles, 1986 , vol. 24, # 9 p. 2581 - 2586 Title/Abstract Full Text View citing articles Show Details
With 5 palladium on charcoal; ammonium formate in methanol; toluene
T=20°C; Inert atmosphere; Overall yield = 72 percent; Overall yield = 8.6 g; Hide Experimental Procedure
Cai, Zhihua; Liu, Guodu; Jiao, Guangjun; Senanayake, Chris H.; Tang, Wenjun
Synthesis (Germany), 2013 , vol. 45, # 24 art. no. SS-2013-H0581-OP, p. 3355 - 3360 Title/Abstract Full Text View citing articles Show Details
Reduction of Nitroalkenes to Oximes 2; General Procedure15
General procedure: To a dry three-necked flask was charged nitroalkene (80 mmol), dryammonium formate (25.2 g, 400 mmol) and MeOH–toluene (1:1, 200 mL). Pd/C (9.5 g, 5 molpercent, wet) was added to the solution under stirring. The resulting mixture was stirred at r.t. until the complete disappearance of the starting material. The mixture was filtered and the filter cake was washed with CH2Cl2 (50 mL). The combined filtrates were concentrated, retreated with CH2Cl2 (50 mL), filtered to remove the insoluble salt, and concentrated. The residue was purified by column chromatography (silica gel, hexanes–EtOAc, 15:1) to afford the desired product as a mixture of E/Z isomers (E/Z 0.8:1 to 2.8:1).
6
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Rx-ID: 37546659 Find similar reactions
With hydroxylamine in water; isopropyl alcohol
T=140°C;
Loiseau, Francis; Beauchemin, Andre M.
Organic Syntheses, 2013 , vol. 90, p. 87 - 95 Title/Abstract Full Text View citing articles Show Details
A
B
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7
Synthesize Find similar Rx-ID: 32288948 Find similar reactions
With glucose-6-phosphate dehydrogenase; G-6-P; wild type pentaerythritol tetranitrate reductase; NADPH in N,Ndimethyl-formamide
T=30°C; 4 h; phosphate bufferInert atmosphereanaerobicEnzymatic reaction; enantioselective reaction;
Toogood, Helen S.; Fryszkowska, Anna; Hulley, Martyn; Sakuma, Michiyo; Mansell, David; Stephens, Gill M.; Gardiner, John M.; Scrutton, Nigel S.
ChemBioChem, 2011 , vol. 12, # 5 p. 738 - 749 Title/Abstract Full Text View citing articles Show Details
A
B
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8
Synthesize Find similar Rx-ID: 29629445 Find similar reactions
A: 41% B: 10%
With palladium 10 on activated carbon; hydrogen in methanol
T=20°C; 0.666667 h;
Durchschein, Katharina; Ferreira-Da Silva, Bianca; Wallner, Silvia; MacHeroux, Peter; Kroutil, Wolfgang; Glueck, Silvia Maria; Faber, Kurt
Green Chemistry, 2010 , vol. 12, # 4 p. 616 - 619 Title/Abstract Full Text View citing articles Show Details
9
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With hydroxylamine in water; isopropyl alcohol
T=110°C; 18.0833 h; Inert atmosphere; regioselective reaction;
Rx-ID: 28612839 Find similar reactions
Moran, Joseph; Pfeiffer, Jennifer Y.; Gorelsky, Serge I.; Beauchemin, Andre M.
Organic Letters, 2009 , vol. 11, # 9 p. 1895 - 1898 Title/Abstract Full Text View citing articles Show Details
A
B
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10
Synthesize Find similar Rx-ID: 28003517 Find similar reactions
A: 5% B: 53%
With hydroxylamine in isopropyl alcohol
T=140°C; intermolecular Cope-type hydroamination; 10 h; microwave irradiation;
Beauchemin, Andre M.; Moran, Joseph; Lebrun, Marie-Eve; Seguin, Catherine; Dimitrijevic, Elena; Zhang, Lili; Gorelsky, Serge I.
Angewandte Chemie - International Edition, 2008 , vol. 47, # 8 p. 1410 - 1413 Title/Abstract Full Text View citing articles Show Details
A
B
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11
Synthesize Find similar Rx-ID: 28495641 Find similar reactions
A: 53% B: 5%
With hydroxylamine in water; isopropyl alcohol
T=140°C; Cope-type hydroamination; Microwave irradiationInert atmosphere; regioselective reaction;
Moran, Joseph; Gorelsky, Serge I.; Dimitrijevic, Elena; Lebrun, Marie-Eve; Bedard, Anne-Catherine; Seguin, Catherine; Beauchemin, Andre M.
Journal of the American Chemical Society, 2008 , vol. 130, # 52 p. 17893 - 17906 Title/Abstract Full Text View citing articles Show Details
A
B
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12
Synthesize Find similar Rx-ID: 10065898 Find similar reactions
A: 5% B: 90%
With hydroxylamine hydrochloride; iron(III) chloride
T=50°C; 0.333333 h;
Eshghi, Hossein; Hassankhani, Asadollah
Organic Preparations and Procedures International, 2005 , vol. 37, # 6 p. 575 - 579 Title/Abstract Full Text View citing articles Show Details
With hydroxylamine hydrochloride; sodium carbonate in tetrahydrofuran; water
2 h; Title compound not separated from byproducts;
Cashman, John R.; Xiong, Yeng N.; Lifen, Xu; Janowsky, Aaron
Journal of Pharmacology and Experimental Therapeutics, 1999 , vol. 288, # 3 p. 1251 - 1260 Title/Abstract Full Text View citing articles Show Details
A
B
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13
Synthesize Find similar Rx-ID: 8621051 Find similar reactions
With indium; ammonium chloride in methanol
Reduction; 3 h; Heating; Title compound not separated from byproducts;
14
Yadav; Subba Reddy; Srinivas; Ramalingam
Synlett, 2000 , # 10 p. 1447 - 1449 Title/Abstract Full Text View citing articles Show Details
Synthesize Find similar 67%
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Rx-ID: 5144276 Find similar reactions
Hwu, Jih Ru; Tseng, Wen Nan; Patel, Himatkumar V.; Wong, Fong Fuh; Horng, Den-Nan; Liaw, Ben Ruey; Lung Ching, Lin
Journal of Organic Chemistry, 1999 , vol. 64, # 7 p. 2211 - 2218 Title/Abstract Full Text View citing articles Show Details
With n-butyllithium; hexamethyl-silane in tetrahydrofuran; hexane
24 h; Ambient temperature;
A
B
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15
Synthesize Find similar Rx-ID: 3984410 Find similar reactions
A: 50 % Spectr. B: 50 % Spectr.
With oxaziridinium tetrafluoroborate derived from N-methyl-1,2,3,4-tetrahydroisoquinoline in dichloromethane
T=0°C; 0.25 h;
Hanquet, Gilles; Lusinchi, Xavier
Tetrahedron, 1994 , vol. 50, # 42 p. 12185 - 12200 Title/Abstract Full Text View citing articles Show Details
16
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Multi-step reaction with 2 steps 1: n-BuNH2 / ethanol / Heating; or HOAc, NH4OAc 2: 91 percent / 0.1 M H2SO4 / propan-2-ol; H2O / 10 - 15 °C / electrolysis View Scheme
17
Rx-ID: 20915506 Find similar reactions
Wessling, Michael; Schaefer, Hans J.
Chemische Berichte, 1991 , vol. 124, # 10 p. 2303 - 2306 Title/Abstract Full Text Show Details
Synthesize Find similar 94%
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With ammonium formate; palladium on activated charcoal in tetrahydrofuran; methanol
0.33 h; Ambient temperature;
Rx-ID: 1553469 Find similar reactions
Kabalka, George W.; Pace, R. David; Wadgaonkar, P.P.
Synthetic Communications, 1990 , vol. 20, # 16 p. 2453 - 2458 Title/Abstract Full Text Show Details
A
B
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18
Synthesize Find similar Rx-ID: 2153011 Find similar reactions
A: 34% B: 35%
With ammonium formate; palladium on activated charcoal in tetrahydrofuran; methanol
2.5 h; Ambient temperature;
Kabalka, George W.; Pace, R. David; Wadgaonkar, P.P.
Synthetic Communications, 1990 , vol. 20, # 16 p. 2453 - 2458 Title/Abstract Full Text Show Details
A
B
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19
Synthesize Find similar Rx-ID: 1553470 Find similar reactions
A: 85% B: 4%
With sodium dithionite; 1,1'-di-n-octyl-4,4'-bipyridinium dibromide in water; ethyl acetate
1 h;
A
20
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Tomioka, Hideo; Ueda, Koichi; Ohi, Hirofumi; Izawa, Yasuji
Chemistry Letters, 1986 , p. 1359 - 1362 Title/Abstract Full Text Show Details
B
Find similar Rx-ID: 1554138 Find similar reactions
A: 79%
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With sodium hydroxide; hydroxylamine in water; isopropyl alcohol
1 h; Ambient temperature;
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Lozynski, Marek; Rusinska-Roszak, Danuta
Polish Journal of Chemistry, 1986 , vol. 60, # 4-6 p. 625 - 630 Title/Abstract Full Text Show Details
A
B
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21
Synthesize Find similar Rx-ID: 1716247 Find similar reactions
A: 3%
With sodium hydroxide; hydroxylamine; tert-butylamine hydrochloride in water; isopropyl alcohol
T=80°C; 2 h;
Lozynski, Marek; Rusinska-Roszak, Danuta
Polish Journal of Chemistry, 1986 , vol. 60, # 4-6 p. 625 - 630 Title/Abstract Full Text Show Details
A
B
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22
Synthesize Find similar Rx-ID: 2070996 Find similar reactions
A: 40% B: 30%
With sodium hypophosphite; palladium on activated charcoal in tetrahydrofuran
0.5 h; Ambient temperature;
A
23
Varma, Rajender S.; Varma, Manju; Kabalka, George W.
Synthetic Communications, 1986 , vol. 16, # 1 p. 91 - 96 Title/Abstract Full Text Show Details
B
Synthesize Find similar Rx-ID: 3935132 Find similar reactions
A: 57%
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Synthesize Find similar
With sodium hydroxide; hydroxylamine in water; isopropyl alcohol
0.25 h; Ambient temperature;
Lozynski, Marek; Rusinska-Roszak, Danuta
Polish Journal of Chemistry, 1986 , vol. 60, # 4-6 p. 625 - 630 Title/Abstract Full Text Show Details
A
B
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24
Synthesize Find similar Rx-ID: 1986971 Find similar reactions
A: 43% B: 6%
With sulfuric acid; toluene-4-sulfonic acid in methanol
T=0 - 5°C; ceramic diaphragm, carbon-rod anode, platinum cathode, 4.5 F/mol, 0.1A, cathode potential -1.45 to -1.65V vs. SCE;
Shono, Tatsuya; Hamaguchi, Hiroshi; Mikami, Hiroshi; Nogusa, Hideo; Kashimura, Shigenori
Journal of Organic Chemistry, 1983 , vol. 48, # 12 p. 2103 - 2105 Title/Abstract Full Text View citing articles Show Details
25
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26
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Rx-ID: 2125434 Find similar reactions
With hydroxylamine hydrochloride; sodium acetate in 1,4-dioxane; perchloric acid; dichloromethane
2 h; Ambient temperature;
Torii, Sigeru; Tanaka, Hideo; Katoh, Tetsuo
Chemistry Letters, 1983 , p. 607 - 610 Title/Abstract Full Text Show Details
Synthesize Find similar 36%
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in nitrobenzene
T=150°C; 1 h; other temperature, other solvent (DMSO), KOH; Product distribution;
Rx-ID: 2102946 Find similar reactions
Trofimov, B. A.; Korostova, S. E.; Sobenina, L. N.; Mikhaleva, A. I.; Bzhezovskii, V. M.; et al.
Chemistry of Heterocyclic Compounds (New York, NY, United States), 1982 , vol. 18, # 2 p. 148 - 152 Khimiya Geterotsiklicheskikh Soedinenii, 1982 , vol. 18, # 2 p. 193 - 198 Title/Abstract Full Text View citing articles Show Details
27
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Rx-ID: 7247825 Find similar reactions
Phenylaceton , H2NOH;
Alvernhe; Laurent
Bulletin de la Societe Chimique de France, 1970 , p. 3003,3004,3007 Full Text Show Details
Phenylpropan-2-on, NH2OH, Pyridin, wss.NaOH (neben d. anti-Isomeren);
Huitric et al.
Journal of Organic Chemistry, 1967 , vol. 32, p. 1661 Full Text View citing articles Show Details
N-Hydroxyamphetamin, Autoxid.;
Lindeke et al.
Acta Pharmaceutica Suecica, 1975 , vol. 12, p. 183,192, 193 Full Text View citing articles Show Details
N-Hydroxyphentermin, Autoxid.;
Lindeke et al.
Acta Pharmaceutica Suecica, 1975 , vol. 12, p. 183,192, 193 Full Text View citing articles Show Details
28
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Rx-ID: 7362548 Find similar reactions
Phenylpropan-2-on, NH2OH, Pyridin, wss.NaOH (neben d. syn-Isomeren);
Huitric et al.
Journal of Organic Chemistry, 1967 , vol. 32, p. 1661 Full Text View citing articles Show Details
entspr. Keton, NH2OH;
Foreman; Siegel; Mrtek
Journal of pharmaceutical sciences, 1969 , vol. 58, # 2 p. 189 - 192 Title/Abstract Full Text View citing articles Show Details
N-Hydroxyamphetamin, Autoxid.;
Lindeke et al.
Acta Pharmaceutica Suecica, 1975 , vol. 12, p. 183,192, 193 Full Text View citing articles Show Details
N-Hydroxyphentermin, Autoxid.;
Lindeke et al.
Acta Pharmaceutica Suecica, 1975 , vol. 12, p. 183,192, 193 Full Text View citing articles Show Details
29
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Rx-ID: 5856922 Find similar reactions
Alvernhe; Laurent
Bulletin de la Societe Chimique de France, 1970 , p. 3003,3004,3007 Full Text Show Details
Phenylaceton , H2NOH;
N-Hydroxy-N-n-propylamphetamin Ie, W., gelbes Quecksilberoxyd;
Beckett; Coutts; Ogunbona
Journal of Pharmacy and Pharmacology, 1974 , vol. 26, # 5 p. 312 - 316 Title/Abstract Full Text View citing articles Show Details
N-Aethyl-N-hydroxyamphetamin Id, W., gelbes Quecksilberoxyd;
Beckett; Coutts; Ogunbona
Journal of Pharmacy and Pharmacology, 1974 , vol. 26, # 5 p. 312 - 316 Title/Abstract Full Text View citing articles Show Details
Beckett; Coutts; Ogunbona
Tetrahedron, 1973 , vol. 29, # 24 p. 4189 - 4193 Title/Abstract Full Text View citing articles Show Details
8a, Chloroperbenzoesaeure, LiAlH4 (u. Homologe);
A
B
C
D
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30
Synthesize Find similar Rx-ID: 1048770 Find similar reactions
With hydrogenchloride; nitrosylchloride
T=20°C; 9 h; Irradiation; Further byproducts given;
Julliard,M.
Bulletin de la Societe Chimique de France, 1970 , p. 2001 - 2004 Full Text View citing articles Show Details
31
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With hydrogen; palladium on activated charcoal in methanol
Rx-ID: 1125567 Find similar reactions
Biela,R. et al.
Journal fuer Praktische Chemie (Leipzig), 1966 , vol. 33, p. 282 - 292 Full Text View citing articles Show Details
32
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Multi-step reaction with 2 steps 1: NOCl, HCl / diethyl ether 2: H2 / Pd-C / methanol View Scheme
Rx-ID: 22423453 Find similar reactions
Biela,R. et al.
Journal fuer Praktische Chemie (Leipzig), 1966 , vol. 33, p. 282 - 292 Full Text View citing articles Show Details
33
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Rx-ID: 8255750 Find similar reactions
Smith
Journal of the American Chemical Society, 1948 , vol. 70, p. 320,322 Journal of the American Chemical Society, 1954 , vol. 76, p. 436,441 Full Text View citing articles Show Details
34
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Rx-ID: 5856923 Find similar reactions
With hydrogenchloride; iron
weiteres Reagens: FeCl3;
Purdue Research Found.
Patent: US2233823 , 1939 ;
With hydrogenchloride; iron
weiteres Reagens: FeCl3;
Purdue Research Found.
Patent: US2233823 , 1939 ;
Full Text Show Details
Full Text Show Details
35
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With hydrogenchloride; diethyl ether
Rx-ID: 668824 Find similar reactions
Dollfus
Chemische Berichte, 1892 , vol. 25, p. 1918 Chemische Berichte, 1893 , vol. 26, p. 1971 Full Text View citing articles Show Details
36
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With ethanol
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Rx-ID: 5856924 Find similar reactions
Dollfus
Chemische Berichte, 1892 , vol. 25, p. 1918 Chemische Berichte, 1893 , vol. 26, p. 1971
Full Text View citing articles Show Details
37
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Rx-ID: 22069718 Find similar reactions
Multi-step reaction with 2 steps 1: alcohol 2: absolute diethyl ether; HCl View Scheme
Dollfus
Chemische Berichte, 1892 , vol. 25, p. 1918 Chemische Berichte, 1893 , vol. 26, p. 1971 Full Text View citing articles Show Details
Multi-step reaction with 2 steps 1: sodium carbonate; aqueous alcohol; hydroxylamine hydrochloride 2: absolute diethyl ether; HCl View Scheme
Dollfus
Chemische Berichte, 1892 , vol. 25, p. 1918 Chemische Berichte, 1893 , vol. 26, p. 1971 Full Text View citing articles Show Details