Reaxys
PubChem
eMolecules
Bioactivities (19670)
Yield
LabNetwork
SigmaAldrich
Reactions (449)
Substances (1)
Targets (1116)
Citations (814)
Conditions
References
199
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2290452 Find similar reactions
With perchloric acid; acetaldehyde; acetone; sodium chloride in water
T=25°C; Irradiation; Rate constantEquilibrium constant;
Keeffe; Kresge; Schepp
Journal of the American Chemical Society, 1990 , vol. 112, # 12 p. 4862 - 4868 Title/Abstract Full Text View citing articles Show Details
With sulfuric acid in water
T=25°C; Rate constantEquilibrium constant;
Dubois, Jaques-Emile; El-Alaoui, Mohiedine; Toullec, Jean
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5393 - 5401 Title/Abstract Full Text View citing articles Show Details
in water
T=25°C; ionic strength: 0.01 M; Equilibrium constant;
Keeffe, J. R.; Kresge, A. J.; Schepp, N. P.
Journal of the American Chemical Society, 1988 , vol. 110, # 6 p. 1993 - 1995 Title/Abstract Full Text View citing articles Show Details
A
B
C
200
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2409820 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
B: 74.9 % Chromat.
With Pd/SiO2 in N,N-dimethyl-formamide
T=59.9°C; 24 h; various solvents, various reagents; Product distribution;
Baba, T.; Nakano, K.; Nishiyama, S.; Tsurya, S.; Masai, M.
Journal of the Chemical Society, Chemical Communications, 1990 , # 4 p. 348 - 349 Title/Abstract Full Text View citing articles Show Details
B: 74.9 % Chromat.
With palladium matal-containing silica-supported catalyst in ethylene glycol dimethyl ether
T=59.9°C; 24 h; Title compound not separated from byproducts;
Baba, T.; Nakano, K.; Nishiyama, S.; Tsurya, S.; Masai, M.
Journal of the Chemical Society, Chemical Communications, 1990 , # 4 p. 348 - 349 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
201
Synthesize Find similar Rx-ID: 2410039 Find similar reactions
A: 90.1%
With oxygen; palladium matal-containing silica-supported catalyst in various solvent(s) T=59.9°C; 24 h; Pd(0) supported on various zeolites , influence of calcination and reaction temperature and of the solvent; Product distributionMechanism;
Baba, Toshide; Nakano, Kaichiro; Nishiyama, Satoru; Tsuruya, Shigeru; Masai, Mitsuo
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1990 , # 7 p. 1113 - 1119 Title/Abstract Full Text View citing articles Show Details
A: 90.1% B: 0.8%
With oxygen; silica gel; palladium in various solvent(s) T=59.9°C; 24 h; solvent; Product distribution;
Baba; Nakano; Nishiyama; Tsuruya; Masai
Journal of the Chemical Society - Series Chemical Communications, 1989 , # 22 p. 1697 - 1699 Title/Abstract Full Text View citing articles Show Details
A: 90.1%
With oxygen; silica gel; palladium in various solvent(s) T=59.9°C; 24 h; Yields of byproduct given;
Baba, Toshide; Nakano, Kaichiro; Nishiyama, Satoru; Tsuruya, Shigeru; Masai, Mitsuo
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1990 , # 7 p. 1113 - 1119 Title/Abstract Full Text View citing articles Show Details
A: 90.1% B: 0.8%
With oxygen; silica gel; palladium in various solvent(s) T=59.9°C; 24 h;
Baba; Nakano; Nishiyama; Tsuruya; Masai
Journal of the Chemical Society - Series Chemical Communications, 1989 , # 22 p. 1697 - 1699 Title/Abstract Full Text View citing articles Show Details
A
B
202
Synthesize Find similar Rx-ID: 2478468 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With sulfuric acid in 1,4-dioxane
T=25°C; Equilibrium constant;
Antonovskii, V. L.; Fedorova, E. V.; Karamyan, S. H.; Ananchenko, S. N.
Doklady Chemistry, 1990 , vol. 311, # 4 p. 75 - 78 Dokl. Akad. Nauk SSSR Ser. Khim., 1990 , vol. 311, # 6 p. 1377 - 1381 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
203
Synthesize Find similar Rx-ID: 8426187 Find similar reactions
With O P=0.9 - 2.3 Torr; Ambient temperature; Rate constantMechanism;
Heinemann-Fiedler, P.; Hoyermann, K.; Rohde, G.
Berichte der Bunsen-Gesellschaft, 1990 , vol. 94, # 11 p. 1400 - 1404 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
204
Synthesize Find similar Rx-ID: 1598360 Find similar reactions
A: 63.6% B: 57.5%
With water; sodium perchlorate
Ambient temperatureelectrolysis;
Synthesize Find similar
Michida; Hatsumura; Sayo
Chemical and Pharmaceutical Bulletin, 1989 , vol. 37, # 12 p. 3393 - 3395 Title/Abstract Full Text View citing articles Show Details
A: 63.6% B: 57.5%
With water; sodium perchlorate
Ambient temperatureelectrolysis, anodic oxidation of several o-nitrophenylthioiminocycloalkanes; Product distribution;
Michida; Hatsumura; Sayo
Chemical and Pharmaceutical Bulletin, 1989 , vol. 37, # 12 p. 3393 - 3395 Title/Abstract Full Text View citing articles Show Details
205
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1817849 Find similar reactions
With hydrogen; Trimethylene glycol in tetrahydrofuran
P=760 Torr; 0.5 h; Ambient temperature; Yield given;
Machinaga, Nobuo; Kibayashi, Chihiro
Tetrahedron Letters, 1989 , vol. 30, # 31 p. 4165 - 4168 Title/Abstract Full Text View citing articles Show Details
206
Synthesize Find similar
Synthesize Find similar
78%
With Wilkinson's catalyst; ethene in chloroform
T=25°C; 16 h;
Campbell, Richard E.; Lochow, Charles F.; Vora, Krishnakant P.; Miller, Roy G.
Journal of the American Chemical Society, 1980 , vol. 102, # 18 p. 5824 - 5830 Title/Abstract Full Text View citing articles Show Details
78%
With [(η2-cyclooctene)4Rh2(μ-Cl)2]; trislt;p-(N,N-dimethylamino)phenylgt;phosphine in dichloromethane 120 h; Ambient temperaturefurther reagents;
Larock,R.C.; Oertle,K.; Potter,G.F.
Journal of the American Chemical Society, 1980 , vol. 102, p. 190 Full Text View citing articles Show Details
With (PPh3)2Co(dppe) in acetonitrile; benzene
T=70°C; 1 h; Yield given;
Vinogradov, M. G.; Tuzikov, A. B.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1989 , vol. 38, # 11.2 p. 2353 - 2356 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1989 , # 11 p. 2565 - 2568 Title/Abstract Full Text View citing articles Show Details
A
207
Rx-ID: 1917527 Find similar reactions
B
Synthesize Find similar Rx-ID: 1984099 Find similar reactions
A: 87.4% B: 0.8%
Synthesize Find similar
Synthesize Find similar
With oxygen; silica gel; palladium in various solvent(s) T=59.9°C; 24 h;
Baba; Nakano; Nishiyama; Tsuruya; Masai
Journal of the Chemical Society - Series Chemical Communications, 1989 , # 22 p. 1697 - 1699 Title/Abstract Full Text View citing articles Show Details
208
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2125614 Find similar reactions
Majerski, Zdenko; Vinkovic, Vladimir
Synthesis, 1989 , # 7 p. 559 - 560 Title/Abstract Full Text Show Details
With oxygen
1) CH2Cl2, -78 deg C, 40 min, irradiation; 2) CH2Cl2, -78 to -10 deg C, 20 min, irradiation; Yield given. Multistep reaction;
209
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2218925 Find similar reactions
With sulfuric acid in butan-1-ol
activation energy; Thermodynamic data;
Danilov, V. A.; Barysheva, N. A.; Postylyakov, A. B.; Rybina, E. A.; Sapozhnikov, Yu. E.
J. Appl. Chem. USSR (Engl. Transl.), 1989 , vol. 62, # 1.2 p. 144 - 147,130 - 133 Title/Abstract Full Text Show Details
A
B
C
210
Synthesize Find similar Rx-ID: 3256487 Find similar reactions
A: 11.3% B: 26.7% C: 20%
Synthesize Find similar
Synthesize Find similar
With sodium perchlorate in acetonitrile
Ambient temperatureelectrolysis;
Synthesize Find similar
Michida; Hatsumura; Sayo
Chemical and Pharmaceutical Bulletin, 1989 , vol. 37, # 12 p. 3393 - 3395 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
211
Synthesize Find similar Rx-ID: 3959822 Find similar reactions
With benzyltrimethylammonium tribromide; sodium acetate in water; acetic acid
T=60°C; 1 h;
Kajigaeshi, Shoji; Kawamukai, Hiroshi; Fujisaki, Shizuo
Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 8 p. 2585 - 2588 Title/Abstract Full Text Show Details
212
Synthesize Find similar 60 % Chromat.
Synthesize Find similar
Rx-ID: 5929739 Find similar reactions
Yamashita, Masakazu; Uchida, Masaya; Tashika, Haruyoshi; Suemitsu, Rikisaku
Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 8 p. 2728 - 2729 Title/Abstract Full Text Show Details
in various solvent(s) 24 h; Ambient temperature;
A
B
213
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1977279 Find similar reactions
Synthesize Find similar
With lead(IV) acetate in benzene
T=80°C; Yield given. Yields of byproduct given;
Synthesize Find similar
Kapustina, N. I.; Popkov, A. Yu.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1988 , vol. 37, p. 2289 - 2293 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1988 , # 11 p. 2538 - 2542 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
214
Synthesize Find similar Rx-ID: 2003321 Find similar reactions
A: 65 % Turnov. C: 12 % Turnov.
With lead(IV) acetate; copper(II) oxide in benzene
T=80°C; 3.5 h; further Cu(II) reagents;
Kapustina, N. I.; Popkov, A. Yu.; Gasanov, R. G.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1988 , vol. 37, # 10 p. 2095 - 2099 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1988 , # 10 p. 2327 - 2331 Title/Abstract Full Text View citing articles Show Details
A: 81 % Turnov. C: 7 % Turnov.
With lead(IV) acetate; copper diacetate in benzene
T=80°C; 3.5 h; further Cu(II) reagents;
Kapustina, N. I.; Popkov, A. Yu.; Gasanov, R. G.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1988 , vol. 37, # 10 p. 2095 - 2099 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1988 , # 10 p. 2327 - 2331 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
215
Synthesize Find similar
Rx-ID: 2003322 Find similar reactions
With lead(IV) acetate; potassium bromide in benzene
T=80°C; Yield given. Yields of byproduct given;
Kapustina, N. I.; Popkov, A. Yu.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1988 , vol. 37, p. 2289 - 2293 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1988 , # 11 p. 2538 - 2542 Title/Abstract Full Text View citing articles Show Details
216
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2526698 Find similar reactions
With n-butyllithium; air; zinc dibromide
1) THF, hexane, -78 deg C, 30 min., 2) -20 deg C, 30 min.; Yield given. Multistep reaction;
Chen, Huai Gu; Knochel, Paul
Tetrahedron Letters, 1988 , vol. 29, # 51 p. 6701 - 6702 Title/Abstract Full Text View citing articles Show Details
multistep reaction; in the presence or in the absence of ZnBr2; Product distribution;
Chen, Huai Gu; Knochel, Paul
Tetrahedron Letters, 1988 , vol. 29, # 51 p. 6701 - 6702 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
217
Synthesize Find similar Rx-ID: 2847972 Find similar reactions
With hydrogenchloride in chloroform
T=50°C; 1 h;
Trapani, Giuseppe; Reho, Antonia; Latrofa, Andrea; Liso, Gaetano
Synthesis, 1988 , # 1 p. 84 - 87 Title/Abstract Full Text Show Details
A
218
B
Synthesize Find similar Rx-ID: 2943396 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With hydrogenchloride in chloroform
T=50°C; 1 h;
Trapani, Giuseppe; Reho, Antonia; Latrofa, Andrea; Liso, Gaetano
Synthesis, 1988 , # 1 p. 84 - 87 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
219
Synthesize Find similar Rx-ID: 2951249 Find similar reactions
With hydrogenchloride in chloroform
T=50°C; 1 h;
Trapani, Giuseppe; Reho, Antonia; Latrofa, Andrea; Liso, Gaetano
Synthesis, 1988 , # 1 p. 84 - 87 Title/Abstract Full Text Show Details
220
Synthesize Find similar 86 % Chromat.
Synthesize Find similar
Rx-ID: 3946286 Find similar reactions
With 2,2'-azo-bisisobutyronitrile; tri-n-butyl-tin hydride
T=60°C; 6 h;
Shibata, Ikuya; Suzuki, Taro; Baba, Akio; Matsuda, Haruo
Journal of the Chemical Society, Chemical Communications, 1988 , # 13 p. 882 - 883 Title/Abstract Full Text View citing articles Show Details
A
B
221
Synthesize Find similar Rx-ID: 3946287 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With N,N,N',N',N'',N''-hexamethylphosphoric triamide; tri-n-butyl-tin hydride
T=60°C; 1 h; Yield given. Yields of byproduct given;
Shibata, Ikuya; Suzuki, Taro; Baba, Akio; Matsuda, Haruo
Journal of the Chemical Society, Chemical Communications, 1988 , # 13 p. 882 - 883 Title/Abstract Full Text View citing articles Show Details
222
Synthesize Find similar 90%
Synthesize Find similar
Rx-ID: 2055966 Find similar reactions
With silica gel; iron(III) chloride
T=20°C; 0.333333 h;
Fadel, Antoine; Yefsah, Ramdane; Salauen, Jacques
Synthesis, 1987 , # 1 p. 37 - 40 Title/Abstract Full Text Show Details
With sulfuric acid in water
T=25°C; Rate constant;
Dubois, Jaques-Emile; El-Alaoui, Mohiedine; Toullec, Jean
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5393 - 5401 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
223
Synthesize Find similar Rx-ID: 2536982 Find similar reactions
A: 7 % Chromat.
With dihydridotetrakis(triphenylphosphine)ruthenium(II) in benzene
T=80°C; Heating;
Minami, Ichiro; Tsuji, Jiro
Tetrahedron, 1987 , vol. 43, # 17 p. 3903 - 3916
B: 93 % Chromat.
Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
224
Synthesize Find similar Rx-ID: 2536983 Find similar reactions
A: 89 % Chromat. B: 4 % Chromat. C: 7 % Chromat.
With Pd(OAc)2*PPh3 in acetonitrile
T=80°C; Heating;
Minami, Ichiro; Tsuji, Jiro
Tetrahedron, 1987 , vol. 43, # 17 p. 3903 - 3916 Title/Abstract Full Text View citing articles Show Details
A: 89 % Chromat. B: 4 % Chromat. C: 7 % Chromat.
With Pd(OAc)2*PPh3 in acetonitrile
T=80°C; Heatingother catalysts and solvents; Product distribution;
Minami, Ichiro; Tsuji, Jiro
Tetrahedron, 1987 , vol. 43, # 17 p. 3903 - 3916 Title/Abstract Full Text View citing articles Show Details
With palladium diacetate; triphenylphosphine in acetonitrile
T=80°C; 4 h; further catalysts, solvents, temperature and reaction time; Product distribution;
Minami, Ichiro; Shimizu, Isao; Tsuji, Jiro
Journal of Organometallic Chemistry, 1985 , vol. 296, p. 269 - 280 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
225
Synthesize Find similar Rx-ID: 2541290 Find similar reactions
A: 71%
With palladium diacetate; triphenylphosphine in acetonitrile
1.5 h; Heating; Yields of byproduct given;
Minami, Ichiro; Nisar, Mohammad; Yuhara, Masami; Shimizu, Isao; Tsuji, Jiro
Synthesis, 1987 , # 11 p. 992 - 998 Title/Abstract Full Text Show Details
A
B
226
Synthesize Find similar Rx-ID: 2630203 Find similar reactions
Synthesize Find similar
Synthesize Find similar
B: 71%
With sodium hydroxide in ethanol
T=25°C;
Katritzky, Alan R.; Fan, Wei-Qiang; Li, Qiao-Ling
Tetrahedron Letters, 1987 , vol. 28, # 11 p. 1195 - 1198 Title/Abstract Full Text View citing articles Show Details
B: 71%
With sodium hydroxide in ethanol
T=25°C; Product distribution;
Katritzky, Alan R.; Fan, Wei-Qiang; Li, Qiao-Ling
Tetrahedron Letters, 1987 , vol. 28, # 11 p. 1195 - 1198 Title/Abstract Full Text View citing articles Show Details
227
Synthesize Find similar
Synthesize Find similar
Rx-ID: 21565924 Find similar reactions
Katritzky, Alan R.; Fan, Wei-Qiang; Li, Qiao-Ling
Tetrahedron Letters, 1987 , vol. 28, # 11 p. 1195 - 1198 Title/Abstract Full Text View citing articles Show Details
Multi-step reaction with 2 steps 1: 70 percent / acetone / 25 °C 2: 71 percent / NaOH / aq. ethanol / 25 °C View Scheme
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
228
Synthesize Find similar Rx-ID: 1869954 Find similar reactions
in 1,2,2-trifluoro-trichloroethane
Synthesize Find similar
Zhao, Cheng-Xue; Jiang, Xi-Kui; Chen, Guo-Fei; Qu, Yan-Ling; Wang, Xian-Shan; Lu, Jian-Ying
T=20°C;
Journal of the American Chemical Society, 1986 , vol. 108, # 11 p. 3132 - 3133 Title/Abstract Full Text View citing articles Show Details
229
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1935094 Find similar reactions
Bakac, Andreja; Espenson, James H.
Journal of the American Chemical Society, 1986 , vol. 108, # 17 p. 5353 - 5354 Title/Abstract Full Text View citing articles Show Details
With lt;(1R,4R,8S,11S)-1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecanegt;nickel; water
T=25°C; Yield given;
A
B
Synthesize Find similar
Synthesize Find similar
230
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003270 Find similar reactions
B: 10.3%
T=115°C; 25 h; autorecycling oxidation, other 10- and 3,10-substituted 8-methylpyrido<2,3-d:6,5-d'>dipyrimidine-2,4,6(3H,10H,7H)-triones; Product distribution;
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
B: 10.3%
in neat (no solvent) T=115°C; 25 h; autorecycling oxidation; Product distribution;
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
231
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003272 Find similar reactions
B: 9%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
232
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003273 Find similar reactions
B: 8.7%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
233
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003274 Find similar reactions
B: 9.8%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize
Synthesize
234
Synthesize
Synthesize
Find similar
Find similar
Rx-ID: 2003275 Find similar reactions
B: 12.7%
Find similar
Find similar
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
235
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003276 Find similar reactions
B: 23.7%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
236
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003277 Find similar reactions
B: 12.5%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
237
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003278 Find similar reactions
B: 14.1%
Synthesize Find similar
Synthesize Find similar
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
238
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003279 Find similar reactions
B: 11.5%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
239
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003280 Find similar reactions
B: 13.2%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
240
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003281 Find similar reactions
B: 10.7%
Synthesize Find similar
Synthesize Find similar
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
241
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003282 Find similar reactions
B: 14.1%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
242
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003283 Find similar reactions
B: 12%
T=115°C; 25 h; autorecycling oxidation; Product distribution;
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
243
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003284 Find similar reactions
B: 8.5%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
244
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2003285 Find similar reactions
B: 8.4%
Moriyama, Kenji; Nagamatsu, Tomohisa; Yoneda, Fumio
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 241 - 243 Title/Abstract Full Text Show Details
T=115°C; 25 h; autorecycling oxidation; Product distribution;
245
Synthesize Find similar 78%
Synthesize Find similar
Rx-ID: 2008016 Find similar reactions
With boron trifluoride diethyl etherate; tetraethylammonium iodide in chloroform
4 h; Heating;
Mandal, Arun K.; Shrotri, P. Y.; Ghogare, A. D.
Synthesis, 1986 , # 3 p. 221 - 222 Title/Abstract Full Text Show Details
A
B
C
D
246
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2246233 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Zhao, Cheng-Xue; Jiang, Xi-Kui; Chen, Guo-Fei; Qu, Yan-Ling; Wang, Xian-Shan; Lu, Jian-Ying
Journal of the American Chemical Society, 1986 , vol. 108, # 11 p. 3132 - 3133 Title/Abstract Full Text View citing articles Show Details
in 1,2,2-trifluoro-trichloroethane
T=20°C;
A
B
Synthesize Find similar
Synthesize Find similar
247
Synthesize Find similar Rx-ID: 2531176 Find similar reactions
With titanium tetrachloride
Hatanaka, Yasuo; Kuwajima, Isao
Tetrahedron Letters, 1986 , vol. 27, # 6 p. 719 - 722 Title/Abstract Full Text Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
248
Synthesize Find similar Rx-ID: 2626690 Find similar reactions
in 1,2,2-trifluoro-trichloroethane
T=20°C;
Synthesize Find similar
Zhao, Cheng-Xue; Jiang, Xi-Kui; Chen, Guo-Fei; Qu, Yan-Ling; Wang, Xian-Shan; Lu, Jian-Ying
Journal of the American Chemical Society, 1986 , vol. 108, # 11 p. 3132 - 3133 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
249
Synthesize Find similar Rx-ID: 26855472 Find similar reactions
With water in water
Kinetics; byproducts: NH3, OH(1-); 25°C, pH 12;; not sepd., detected by UV spectra;;
Bakac, Andreja; Espenson, James H.
Journal of the American Chemical Society, 1986 , vol. 108, # 17 p. 5353 - 5354 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
E
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
250
Synthesize Find similar Rx-ID: 1917529 Find similar reactions
With N-dodecane; Co(N2)(PPh3)3H in benzene
T=20°C; influence of catalyst employed, temperature and time effects; further catalysts; further temperature; Product distribution;
Vinogradov, M. G.; Tuzikov, A. B.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1985 , vol. 34, # 2 p. 325 - 329 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1985 , # 2 p. 356 - 361 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
251
Synthesize Find similar Rx-ID: 1917530 Find similar reactions
With C108H90Co2N2P6; 1,2-bis-(diphenylphosphino)ethane in benzene
T=70°C; 1 h; nature of the ligand, solvent and temperature dependence; Product distributionMechanism;
Vinogradov, M. G.; Tuzikov, A. B.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1985 , vol. 34, # 11 p. 2369 - 2374 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1985 , # 11 p. 2557 - 2562
Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
252
Synthesize Find similar Rx-ID: 1945855 Find similar reactions
With n-butyllithium; chloro-trimethyl-silane; water
-110 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
Cooke, Manning P.; Houpis, Ioannis N.
Tetrahedron Letters, 1985 , vol. 26, # 41 p. 4987 - 4990 Title/Abstract Full Text View citing articles Show Details
253
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2154460 Find similar reactions
With hydroxide in 1,4-dioxane; water
T=25.1°C; Rate constant;
Elvidge, John A.; Jones, John R.; Russell, Jeremy C.; Wiseman, Alan; Coombs, Maurice M.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1985 , p. 563 - 566 Title/Abstract Full Text Show Details
254
Synthesize Find similar
With hydrogenchloride in methanol
5 h; Heating; Yield given;
Synthesize Find similar
Rx-ID: 2482581 Find similar reactions
Ogura, Katsuyuki; Ohtsuki, Kazuo; Nakamura, Masami; Yahata, Nobuhiro; Takahashi, Kazumasa; Iida, Hirotada
Tetrahedron Letters, 1985 , vol. 26, # 20 p. 2455 - 2458 Title/Abstract Full Text View citing articles Show Details
255
Synthesize Find similar
71 % Chromat.
Synthesize Find similar
Rx-ID: 2533124 Find similar reactions
With n-butyllithium in tetrahydrofuran
T=-78°C;
Cooke, Manning P.; Houpis, Ioannis N.
Tetrahedron Letters, 1985 , vol. 26, # 41 p. 4987 - 4990 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
256
Synthesize Find similar Rx-ID: 2591967 Find similar reactions
With hydrogenchloride in chloroform
T=23°C; 5 h; Product distribution;
Bobowski; Shavel Jr.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, # 6 p. 1679 - 1688 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
257
Synthesize Find similar Rx-ID: 3531693 Find similar reactions
With oxygen; p-benozquinone; palladium dichloride in ethanol
T=30°C; P=860 Torr; 8 h; Product distribution;
Takehira, Katsuomi; Hayakawa, Takashi; Orita, Hideo
Chemistry Letters, 1985 , p. 1835 - 1838 Title/Abstract Full Text Show Details
A
B
C
258
Synthesize Find similar
Synthesize Find similar
Rx-ID: 3959818 Find similar reactions
A: 10% C: 54%
Synthesize Find similar
With dihydridotetrakis(triphenylphosphine)ruthenium(II) in benzene
T=100°C; 22 h;
Synthesize Find similar
Synthesize Find similar
Minami, Ichiro; Shimizu, Isao; Tsuji, Jiro
Journal of Organometallic Chemistry, 1985 , vol. 296, p. 269 - 280 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
259
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1657247 Find similar reactions
A: 12.5% B: 2.2 g
Lochead, Alistair W.; Proctor, George R.; Caton, Michael P. L.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1984 , # 11 p. 2477 - 2489 Title/Abstract Full Text View citing articles Show Details
in acetonitrile
21 h; Heating;
A
B
Synthesize Find similar
Synthesize Find similar
260
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1906354 Find similar reactions
Gas phase. Determ. by ICR spect.; Equilibrium constantThermodynamic data;
Bouchoux, G.; Houriet, R.
Tetrahedron Letters, 1984 , vol. 25, # 50 p. 5755 - 5758 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
261
Synthesize Find similar Rx-ID: 1978586 Find similar reactions
With oxygen; Nitrous oxide in water
IrradiationpH=6.5; Rate constantMechanism;
Zegota, Henryk; Schuchmann, Man Nien; von Sonntag, Clemens
Journal of Physical Chemistry, 1984 , vol. 88, # 23 p. 5589 - 5593 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
262
Synthesize Find similar Rx-ID: 1999264 Find similar reactions
With oxygen; Nitrous oxide in water
IrradiationpH=6.5; Product distribution;
Zegota, Henryk; Schuchmann, Man Nien; von Sonntag, Clemens
Journal of Physical Chemistry, 1984 , vol. 88, # 23 p. 5589 - 5593 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
E
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
263
Synthesize Find similar Rx-ID: 2003317 Find similar reactions
A: 2 % Turnov. B: 5 % Turnov.
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; other ratio of cyclopentanol : LTA-Cu(OAc)2; Product distribution;
Nikishin, G. I.; Kapustina, N. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 6 p. 1235 - 1239 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 6 p. 1345 - 1348 Title/Abstract Full Text View citing articles Show Details
C: 59 % Turnov. D: 10 % Turnov. E: 2 % Turnov.
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
264
Synthesize Find similar Rx-ID: 2003318 Find similar reactions
A: 2 % Turnov. B: 80 % Turnov. C: 3 % Turnov. D: 8 % Turnov.
With pyridine; lead(IV) acetate; lithium chloride in benzene
T=65 - 70°C; 0.25 h; Further byproducts given;
Nikishin, G. I.; Kapustina, N. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 6 p. 1235 - 1239 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 6 p. 1345 - 1348 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
265
Synthesize Find similar Rx-ID: 2003319 Find similar reactions
A: 80 % Turnov. B: 3 % Turnov. C: 8 % Turnov. D: 3 % Turnov.
With pyridine; lead(IV) acetate; lithium chloride in benzene
T=65 - 70°C; 0.25 h; Further byproducts given;
Nikishin, G. I.; Kapustina, N. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 6 p. 1235 - 1239 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 6 p. 1345 - 1348 Title/Abstract Full Text View citing articles Show Details
A
B
266
Synthesize Find similar Rx-ID: 2054942 Find similar reactions
A: 91.0 % Turnov. B: 0.25 % Turnov.
Synthesize Find similar
Synthesize Find similar
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; 2 h;
Kapustina, N. I.; Spektor, S. S.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 12 p. 2490 - 2497 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 12 p. 2721 - 2729 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
267
Synthesize Find similar Rx-ID: 2055083 Find similar reactions
A: 94.0 % Turnov. B: 0.60 % Turnov.
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; 2 h;
Kapustina, N. I.; Spektor, S. S.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 12 p. 2490 - 2497 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 12 p. 2721 - 2729 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
268
Synthesize Find similar Rx-ID: 2104493 Find similar reactions
With oxygen; methylene blue in dichloromethane
T=15°C; 5 h; Irradiation;
Ando, Wataru; Sato, Rikiya; Sonobe, Hideki; Akasaka, Takeshi
Tetrahedron Letters, 1984 , vol. 25, # 8 p. 853 - 856 Title/Abstract Full Text View citing articles Show Details
269
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2147523 Find similar reactions
With sulfuric acid in ethanol
15 h; Ambient temperature;
Ogura, K.; Yamashita, M.; Suzuki, M.; Furukawa, S.; Tsuchinashi, G.
Bulletin of the Chemical Society of Japan, 1984 , vol. 57, # 6 p. 1637 - 1642 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
270
Synthesize Find similar Rx-ID: 2147617 Find similar reactions
A: 19.0 % Turnov. B: 71.5 % Turnov.
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; 2 h;
Kapustina, N. I.; Spektor, S. S.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 12 p. 2490 - 2497 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 12 p. 2721 - 2729 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
271
Synthesize Find similar Rx-ID: 2149337 Find similar reactions
A: 97.0 % Turnov. B: 0.30
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; 2 h;
Kapustina, N. I.; Spektor, S. S.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 12 p. 2490 - 2497 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 12 p. 2721 - 2729
% Turnov.
Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
272
Synthesize Find similar Rx-ID: 2188513 Find similar reactions
A: 85.5 % Turnov. B: 8.5 % Turnov.
With pyridine; lead(IV) acetate; copper diacetate in benzene
T=80°C; 2 h;
Kapustina, N. I.; Spektor, S. S.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, # 12 p. 2490 - 2497 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 12 p. 2721 - 2729 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
273
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2409818 Find similar reactions
A: 15 % Chromat. B: 16 % Chromat. C: 72 % Chromat.
Tsuji, Jiro; Minami, Ichiro; Shimizu, Isao; Kataoka, Hideaki
Chemistry Letters, 1984 , p. 1133 - 1136 Title/Abstract Full Text Show Details
With [Pd(1,2-bis(diphenylphosphino)ethane)(OAc)2] in acetonitrile
T=80°C; var. catalyst, solvent;; Product distribution;
274
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2536981 Find similar reactions
76 % Chromat.
With palladium diacetate in acetonitrile
T=80°C; 2 h;
Tsuji, Jiro; Minami, Ichiro; Shimizu, Isao
Tetrahedron Letters, 1984 , vol. 25, # 26 p. 2791 - 2792 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
275
Synthesize Find similar
Synthesize Find similar
Rx-ID: 3740570 Find similar reactions
Bouchoux, G.; Houriet, R.
Tetrahedron Letters, 1984 , vol. 25, # 50 p. 5755 - 5758 Title/Abstract Full Text View citing articles Show Details
Gas phase. Determ. by ICR spect.; Equilibrium constantThermodynamic data;
276
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5929734 Find similar reactions
Saunders, David R.; Mawby, Roger J.
Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1984 , p. 2133 - 2136 Title/Abstract Full Text View citing articles Show Details
in various solvent(s) T=-50.1°C;
277
Synthesize Find similar
Rx-ID: 1543872 Find similar reactions
With hydrogenchloride; Aliquatreg; 336
Synthesize Find similar
Synthesize Find similar
Ogura, Katsuyuki; Yahata, Nobuhiro; Hashizume, Kimitoshi; Tsuyama, Koichi; Takahashi, Kazumasa; Iida, Hirotada
1.) toluene, 50 percent NaOH, 60 deg C; 2.) methanol, reflux; Yield given. Multistep reaction;
Chemistry Letters, 1983 , p. 767 - 770 Title/Abstract Full Text Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
278
Synthesize Find similar Rx-ID: 1698894 Find similar reactions
Lin, Yingrui; Lu, Xiyan
Journal of Organometallic Chemistry, 1983 , vol. 251, # 3 p. 321 - 326 Title/Abstract Full Text View citing articles Show Details
With trans-Mo(N2)2(1,2-bis(diphenylphosphino)ethane)2 in benzene
3 h; Heatingother acyclic and cyclic allylic alcohols; Product distributionMechanism;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
279
Synthesize Find similar Rx-ID: 1917531 Find similar reactions
A: 38 % Turnov.
With cobalt in tetrahydrofuran
T=20°C; 2 h; other reagent; Product distribution;
Vinogradov, M. G.; Tuzikov, A. B.; Nikishin, G. I.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1983 , vol. 32, p. 1535 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1983 , # 7 p. 1686 - 1687 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
280
Rx-ID: 2140361 Find similar reactions
With air in various solvent(s) T=160°C; P=760 Torr; Yield given. Yields of byproduct given;
Druliner, J. D.; Kitson, F. G.; Rudat, M. A.; Tolman, C. A.
Journal of Organic Chemistry, 1983 , vol. 48, # 25 p. 4951 - 4953 Title/Abstract Full Text View citing articles Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
281
Synthesize Find similar Rx-ID: 2140362 Find similar reactions
With air in various solvent(s) T=160°C; P=760 Torr; var. cond., var. solv.; deuter. comp.; Product distributionMechanism;
Druliner, J. D.; Kitson, F. G.; Rudat, M. A.; Tolman, C. A.
Journal of Organic Chemistry, 1983 , vol. 48, # 25 p. 4951 - 4953 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
282
Synthesize Find similar Rx-ID: 3120589 Find similar reactions
With soda-lime
McHintosh, John M.; Pillon, Lilianna Z.; Acquaah, Samuel O.; Green, James R.; White, Graham S.
Canadian Journal of Chemistry, 1983 , vol. 61, p. 2016 - 2021 Title/Abstract Full Text Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
283
Synthesize Find similar Rx-ID: 7452267
Find similar reactions
A: 11 % Turnov. B: 32 % Turnov. C: 29 % Turnov. D: 11 % Turnov.
Galoci, Jan; Prochazka, Milos; Klinotova, Eva
Collection of Czechoslovak Chemical Communications, 1983 , vol. 48, # l p. 1729 - 1733 Title/Abstract Full Text Show Details
T=270°C; other temperature; Product distribution;
A
B
Synthesize Find similar
Synthesize Find similar
284
Rx-ID: 25059834 Find similar reactions
Schering Aktiengesellschaft
Patent: US4407823 A1, 1983 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
13:EXAMPLE 13
EXAMPLE 13 As described in Example 12(a), 2-[4-(2-oxopentylidenemethyl)phenyl]propionic acid, m.p. 158°, is obtained from cyclopentanone and 2-(4-formylphenyl)propionic acid. A
B
Synthesize Find similar
Synthesize Find similar
285
Synthesize Find similar Rx-ID: 26854153 Find similar reactions
A: 83% B: 90%
With CO in toluene
toluene soln. of Mo complex placed in autoclave under 50 atm CO pressure, stirred at 90°C for 12 h; distn., trapping at -78°C;
A
B
Diversi, Pietro; Ingrosso, Giovanni; Lucherini, Antonio; Porzio, William; Zocchi, Marcello
Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1983 , p. 967 - 974 Title/Abstract Full Text Show Details
286
Synthesize Find similar Rx-ID: 1507406 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Karakhanov, E. A.; Karzhavina, N. P.; Brezhnev, L. Yu.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 1 p. 191 - 192 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 1 p. 203 - 204 Title/Abstract Full Text View citing articles Show Details
T=500 - 590°C; thermal transformation;
A
B
C
D
E
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
287
Synthesize Find similar Rx-ID: 1514376 Find similar reactions
Karakhanov, E. A.; Karzhavina, N. P.; Brezhnev, L. Yu.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 1 p. 191 - 192 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 1 p. 203 - 204 Title/Abstract Full Text View citing articles Show Details
T=500 - 590°C; thermal transformation;
288
Synthesize Find similar
80%
Synthesize Find similar
With trimethylsilyl bromide; dimethyl sulfoxide in tetrachloromethane
T=75 - 80°C; 24 h;
Rx-ID: 1516212 Find similar reactions
Olah, George A.; Narang, Subbash C.; Mehrotra, Ashok K.
Synthesis, 1982 , # 11 p. 965 - 966 Title/Abstract Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
289
Synthesize Find similar Rx-ID: 1917528 Find similar reactions
With RhCl(PMe3)3
T=50°C; 2 h; Yield given. Yields of byproduct given;
Milstein, David
Journal of the Chemical Society, Chemical Communications, 1982 , # 23 p. 1357 - 1358 Title/Abstract Full Text View citing articles Show Details
With RhCl(PMe3)3
T=50°C; 2 h; Product distributionMechanism;
Milstein, David
Journal of the Chemical Society, Chemical Communications, 1982 , # 23 p. 1357 - 1358 Title/Abstract Full Text View citing articles Show Details
290
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2108317 Find similar reactions
10%
in ethanol; water
T=160°C; 168 h; 50percent CF3CH2OH, NEt4Br; Mechanism;
Hanack, Michael; Maerkl, Rainer; Martinez, Antonio Garcia
Chemische Berichte, 1982 , vol. 115, # 2 p. 772 - 782 Title/Abstract Full Text Show Details
With lutidine; water in ethanol
T=151 - 176.5°C; Kinetics;
Pfeifer,W.D. et al.
Journal of the American Chemical Society, 1971 , vol. 93, # 6 p. 1513 - 1516 Full Text View citing articles Show Details
A
B
C
D
Synthesize
Synthesize
Synthesize
Synthesize
291
Synthesize Find similar
Synthesize Find similar
Find similar
Rx-ID: 2409984 Find similar reactions
B: 43 % Chromat. D: 12 % Chromat.
With antimony(III) chloride in dichloromethane
T=0°C; 1 h;
Find similar
Find similar
Find similar
Tirpak, Robin E.; Rathke, Michael W.
Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5099 - 5102 Title/Abstract Full Text View citing articles Show Details
292
Synthesize Find similar
94%
Synthesize Find similar
Rx-ID: 2819523 Find similar reactions
With hydrogenchloride in methanol
3 h; Heating;
Ogura, Katsuyuki; Suzuki, Michiyo; Watanabe, Jun-ichi; Yamashita, Mitsuo; Iida, Hirotada; Tsuchihashi, Gen-ichi
Chemistry Letters, 1982 , p. 813 - 814 Title/Abstract Full Text Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
293
Synthesize Find similar Rx-ID: 3531639 Find similar reactions
A: 4 % Chromat. B: 27 % Chromat. C: 1 % Chromat. D: 3 % Chromat.
294
With Pd(NO2)Cl(MeCN)2 in dichloromethane
T=20°C; 6 h; other cycloalkenes; Product distribution;
Andrews,M.A.; Cheng,C.W.
Journal of the American Chemical Society, 1982 , vol. 104, p. 4268 Full Text View citing articles Show Details
Synthesize Find similar
Synthesize Find similar
Rx-ID: 6727465 Find similar reactions
With carbon dioxide; zinc oxide
multistep reaction; Product distribution;
Vasina, T. V.; Chelmakova, S. A.; Lutovinova, V. N.; Liberman, A. L.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1982 , vol. 31, # 10 p. 2046 - 2048 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1982 , # 10 p. 2325 - 2327 Title/Abstract Full Text View citing articles Show Details
295
Synthesize Find similar
Synthesize Find similar
Rx-ID: 25041128 Find similar reactions
With hydrogenchloride; sodium chloride; sodium carbonate in butan-1-ol
International Flavors and Fragrances Inc.
Patent: US4260830 A1, 1981 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
II.C:EXAMPLE II-C STR37
EXAMPLE II-C STR37 Into a 250 ml reaction flask equipped with mechanical stirrer, immersion thermometer, water-cooled condenser and heating mantle is placed 38.73 grams (0.23 moles) of the aldol condensation product of cyclopentanone and n-valeraldehyde produced according to Example II-A and 176.4 ml of 5percent hydrogen chloride in nbutanol (8.4 ml of 38percent HCl in 168 ml n-butanol). The reaction mass is heated with stirring to reflux and refluxed until the ratio of endo:exo isomer is 13:1 (87.4percent endo:6.7percent exo) monitored on a 6'*1/4" SE-30 glass packed GLC column). The time of reaction is 165 minutes. At the end of the 165-minute period the reaction apparatus is shut down and the reaction mass is washed with 1 volume of saturated sodium chloride solution followed by 1 volume of 10percent sodium carbonate solution and 3 volumes of saturated sodium chloride solution. The product is then dried over anhydrous sodium sulfate to yield 249 grams of crude. The crude material is distilled under vacuum over a rush-over head as follows: Yield of product is 17.66 grams (50.52percent).
With hydrogenchloride; sodium chloride; sodium carbonate in butan-1-ol
International Flavors and Fragrances Inc.
Patent: US4310701 A1, 1982 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
II.C:EXAMPLE II-C STR57
EXAMPLE II-C STR57 Into a 250 ml reaction flask equipped with mechanical stirrer, immersion thermometer, water-cooled condenser and heating mantle is placed 38.73 grams (0.23 moles) of the aldol condensation product of cyclopentanone and n-valeraldehyde produced according to Example II-A and 176.4 ml of 5percent hydrogen chloride in nbutanol (8.4 ml of 38percent HCl in 168 ml n-butanol). The reaction mass is heated with stirring to reflux and refluxed until the ratio of endo:exo isomer is 13:1 (87.4percent endo:6.7percent exo) monitored on a 6'*1/4" SE-30 glass packed GLC column). The time of reaction is 165 minutes. At the end of the 165-minute period the reaction apparatus is shut down and the reaction mass is washed with 1 volume of saturated sodium chloride solution followed by 1 volume of 10percent sodium carbonate solution and 3 volumes of saturated sodium chloride solution. The product is then dried over anhydrous sodium sulfate to yield 249 grams of crude. The crude material is distilled under vacuum over a rush-over head as follows: Yield of product is 17.66 grams (50.52percent). A
296
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1480640 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Bromilow, J.; Abboud, J. L. M.; Lebrilla, C. B.; Taft, R. W.; Scorrano, G.; Lucchini V.
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5448 - 5453 Title/Abstract Full Text View citing articles Show Details
T=24.9°C; ΔG0; Thermodynamic data;
A
B
Synthesize Find similar
Synthesize Find similar
297
Synthesize Find similar Rx-ID: 1480652 Find similar reactions
T=24.9°C; ΔG0; Thermodynamic data;
Synthesize Find similar
Bromilow, J.; Abboud, J. L. M.; Lebrilla, C. B.; Taft, R. W.; Scorrano, G.; Lucchini V.
Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5448 - 5453 Title/Abstract Full Text View citing articles Show Details