Reaxys
PubChem
eMolecules
Reactions (41)
Yield
Substances (3)
Citations (41)
Conditions
References A
B
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1
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A: 85% B: 5%
With hydrogen in water
T=270°C; P=16501.7 Torr; 3 h;
Huang, Yao-Bing; Yan, Long; Chen, Meng-Yuan; Guo, Qing-Xiang; Fu, Yao
Green Chemistry, 2015 , vol. 17, # 5 p. 3010 - 3017 Title/Abstract Full Text View citing articles Show Details
A
2
B
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A: 68% B: 7%
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With hydrogen in water
T=270°C; P=16501.7 Torr; 4 h;
Huang, Yao-Bing; Yan, Long; Chen, Meng-Yuan; Guo, Qing-Xiang; Fu, Yao
Green Chemistry, 2015 , vol. 17, # 5 p. 3010 - 3017 Title/Abstract Full Text View citing articles Show Details
3
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Rx-ID: 28595807 Find similar reactions
76 %Chromat.
With hydrogen in dichloromethane
T=20°C; P=5171.62 Torr; 48 h;
Polshettiwar, Vivek; Baruwati, Babita; Varma, Rajender S.
Green Chemistry, 2009 , vol. 11, # 1 p. 127 - 131 Title/Abstract Full Text View citing articles Show Details
99 %Chromat.
With copper(II)-citrate; 1,3,5,7-tetra-azatricyclo[5.1.1.13,5]decane; hypophosphorous ether in water; N,N-dimethyl-formamide
T=130°C; 6 h; Inert atmosphereGreen chemistry; chemoselective reaction;
Cao, Huanyang; Chen, Tieqiao; Zhou, Yongbo; Han, Daoqing; Yin, Shuang-Feng; Han, Li-Biao
Advanced Synthesis and Catalysis, 2014 , vol. 356, # 4 p. 765 - 769 Title/Abstract Full Text View citing articles Show Details
With carbon monoxide; water in ethanol
T=80°C; P=7600.51 Torr; 12 h; AutoclaveGreen chemistry; chemoselective reaction;
Li, Shu-Shuang; Liu, Xiang; Liu, Yong-Mei; He, He-Yong; Fan, Kang-Nian; Cao, Yong
Chemical Communications, 2014 , vol. 50, # 42 p. 5626 - 5628 Title/Abstract Full Text View citing articles Show Details
4
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Rx-ID: 33579965 Find similar reactions
81%
With copper (II) acetate monohydrate; tert-butyl alcohol; (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(bis(3,5-bis(trifluoromethyl)phenyl)phosphine) in tetrahydrofuran
T=65°C; 20 h; Inert atmosphere; chemoselective reaction;
Semba, Kazuhiko; Fujihara, Tetsuaki; Xu, Tinghua; Terao, Jun; Tsuji, Yasushi
Advanced Synthesis and Catalysis, 2012 , vol. 354, # 8 p. 1542 - 1550 Title/Abstract Full Text View citing articles Show Details
Multi-step reaction with 2 steps 1.1: tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; C69H56N2O2*BF4(1-)*H(1+) / tetrahydrofuran / 0.17 h / 20 °C / |Inert atmosphere 1.2: 0.5 h / 20 °C / |Inert atmosphere 2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 20 °C / |Inert atmosphere View Scheme
Miller, Zachary D.; Montgomery, John
Organic Letters, 2014 , vol. 16, # 20 p. 5486 - 5489 Title/Abstract Full Text View citing articles Show Details
Multi-step reaction with 2 steps 1.1: tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; 1,3-bis{2,6-bis(diphenylmethyl)-4-methylphenyl}-imidazolin-2-ylidene / tetrahydrofuran / 0.17 h / 20 °C / |Inert atmosphere 1.2: 2 h / 20 °C / |Inert atmosphere 2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 20 °C / |Inert atmosphere View Scheme
Miller, Zachary D.; Montgomery, John
Organic Letters, 2014 , vol. 16, # 20 p. 5486 - 5489 Title/Abstract Full Text View citing articles Show Details
5
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Rx-ID: 39062508 Find similar reactions
With tetrabutyl ammonium fluoride in tetrahydrofuran
T=20°C; 0.25 h; Inert atmosphere; regioselective reaction;
Miller, Zachary D.; Montgomery, John
Organic Letters, 2014 , vol. 16, # 20 p. 5486 - 5489 Title/Abstract Full Text View citing articles Show Details
6
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T=20°C; 0.25 h; Inert atmosphere; regioselective reaction;
7
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Rx-ID: 39062575 Find similar reactions
Miller, Zachary D.; Montgomery, John
Organic Letters, 2014 , vol. 16, # 20 p. 5486 - 5489 Title/Abstract Full Text View citing articles Show Details
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Rx-ID: 30188390 Find similar reactions
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5%
With C20H14Cl5FeN2O2 in diethyl ether
T=20°C;
Reckling, Amy M.; Martin, Dana; Dawe, Louise N.; Decken, Andreas; Kozak, Christopher M.
Journal of Organometallic Chemistry, 2011 , vol. 696, # 3 p. 787 - 794 Title/Abstract Full Text View citing articles Show Details
5%
With N-dodecane; C20H14Cl5FeN2O2 in diethyl ether
T=20°C; 0.5 h; Schlenk technique; Catalytic behavior; Hide Experimental Procedure
UNIVERSITY OF PRINCE EDWARD ISLAND; GENESIS GROUP INC.; SHAVER, Michael, P.; KOZAK, Christopher, M.
Patent: WO2013/53046 A1, 2013 ; Location in patent: Paragraph 00193-00195 ; Title/Abstract Full Text Show Details
4.5.9:Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes
General procedure: [00193] Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes[001 4] Grignard cross-coupling reactions were carried out using tetradentate amine (bisphenolate) iron complexes. The synthesis and characterization of the tetradentate amine- bis(phenolate) iron complexes employed in the following cross-coupling reactions are described in Example 2 above.[00195] Catalyst (iron complex) (0.1 mmol, 5.0 molpercent) in CH2C12 (3 L) was added to a Schlenk flask followed by removal of the solvent in vacuo. To the catalyst were added Et20 (5 mL), alkyl halide (2.0 mmol) and dodecane (2.0 mmol as internal standard) and the solution was stirred at room temperature. Grignard (4.0 mmol) was added and the resulting mixture was stirred for 30 minutes. The reaction was quenched with HC1 (aq., 2 M, 5 mL) and the organic phase was extracted with Et20 (1 x 5 mL) and dried over MgS04. The mixture was analyzed by GC-MS and quantified using lH NMR and/or GC. NMR samples were prepared by careful removal of solvent under vacuum and dissolving the residue in CDC13.Table 5: Cross-coupling catalysis data
8
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Rx-ID: 30188391 Find similar reactions
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7%
With C20H14Cl5FeN2O2 in diethyl ether
T=20°C;
Reckling, Amy M.; Martin, Dana; Dawe, Louise N.; Decken, Andreas; Kozak, Christopher M.
Journal of Organometallic Chemistry, 2011 , vol. 696, # 3 p. 787 - 794 Title/Abstract Full Text View citing articles Show Details
7%
With N-dodecane; C20H14Cl5FeN2O2 in diethyl ether
T=20°C; 0.5 h; Schlenk technique; Catalytic behavior; Hide Experimental Procedure
UNIVERSITY OF PRINCE EDWARD ISLAND; GENESIS GROUP INC.; SHAVER, Michael, P.; KOZAK, Christopher, M.
Patent: WO2013/53046 A1, 2013 ; Location in patent: Paragraph 00193-00195 ; Title/Abstract Full Text Show Details
4.5.10:Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes
General procedure: [00193] Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes[001 4] Grignard cross-coupling reactions were carried out using tetradentate amine (bisphenolate) iron complexes. The synthesis and characterization of the tetradentate amine- bis(phenolate) iron complexes employed in the following cross-coupling reactions are described in Example 2 above.[00195] Catalyst (iron complex) (0.1 mmol, 5.0 molpercent) in CH2C12 (3 L) was added to a Schlenk flask followed by removal of the solvent in vacuo. To the catalyst were added Et20 (5 mL), alkyl halide (2.0 mmol) and dodecane (2.0 mmol as internal standard) and the solution was stirred at room temperature. Grignard (4.0 mmol) was added and the resulting mixture was stirred for 30 minutes. The reaction was quenched with HC1 (aq., 2 M, 5 mL) and the organic phase was extracted with Et20 (1 x 5 mL) and dried over MgS04. The mixture was analyzed by GC-MS and quantified using lH NMR and/or GC. NMR samples were prepared by careful removal of solvent under vacuum and dissolving the residue in CDC13.Table 5: Cross-coupling catalysis data
9
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Rx-ID: 35372020 Find similar reactions
3%
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With N-dodecane; C20H14Cl5FeN2O2 in diethyl ether
T=20°C; 0.5 h; Schlenk technique; Catalytic behavior; Hide Experimental Procedure
UNIVERSITY OF PRINCE EDWARD ISLAND; GENESIS GROUP INC.; SHAVER, Michael, P.; KOZAK, Christopher, M.
Patent: WO2013/53046 A1, 2013 ; Location in patent: Paragraph 00193-00195 ; Title/Abstract Full Text Show Details
4.5.8:Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes
General procedure: [00193] Example 4: Cross-coupling catalysis with tetradentate amine ('bisphenolate') iron complexes[001 4] Grignard cross-coupling reactions were carried out using tetradentate amine (bisphenolate) iron complexes. The synthesis and characterization of the tetradentate amine- bis(phenolate) iron complexes employed in the following cross-coupling reactions are described in Example 2 above.[00195] Catalyst (iron complex) (0.1 mmol, 5.0 molpercent) in CH2C12 (3 L) was added to a Schlenk flask followed by removal of the solvent in vacuo. To the catalyst were added Et20 (5 mL), alkyl halide (2.0 mmol) and dodecane (2.0 mmol as internal standard) and the solution was stirred at room temperature. Grignard (4.0 mmol) was added and the resulting mixture was stirred for 30 minutes. The reaction was quenched with HC1 (aq., 2 M, 5 mL) and the organic phase was extracted with Et20 (1 x 5 mL) and dried over MgS04. The mixture was analyzed by GC-MS and quantified using lH NMR and/or GC. NMR samples were prepared by careful removal of solvent under vacuum and dissolving the residue in CDC13.Table 5: Cross-coupling catalysis data
10
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Rx-ID: 35646412 Find similar reactions
70%
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With titanium tetrachloride in dichloromethane
T=50°C; 0.25 h;
Hassner, Alfred; Bandi, Chennakesava Reddy
Synlett, 2013 , vol. 24, # 10 art. no. ST-2013-B0058-L, p. 1275 - 1279 Title/Abstract Full Text View citing articles Show Details
11
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Rx-ID: 31936010 Find similar reactions
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85 %Chromat.
Stage #1: ethylene,methyl acetate With manganese; trifluoroacetic acid; cobalt(II) dibromide in acetonitrile
T=20°C; 0.0833333 h; Stage #2: 1-trans-IODO-4-CYCLOHEXYL With pyridine in acetonitrile
T=80°C;
Qian, Xin; Auffrant, Audrey; Felouat, Abdellah; Gosmini, Corinne
Angewandte Chemie - International Edition, 2011 , vol. 50, # 44 p. 10402 - 10405 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
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12
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Ouchi, Akihiko; Liu, Suyou; Li, Zhong; Kumar, S. Ajaya; Suzuki, Toshiaki; Hyugano, Takeshi; Kitahara, Haruo
Journal of Organic Chemistry, 2007 , vol. 72, # 23 p. 8700 - 8706 Title/Abstract Full Text View citing articles Show Details
in cyclohexane
T=20°C; Photolysis; Product distribution; Further Variations:reaction times;
13
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Rx-ID: 9845647 Find similar reactions
Font, Rafael; Aracil, Ignacio; Fullana, Andres; Conesa, Juan A.
Chemosphere, 2004 , vol. 57, # 7 p. 615 - 627 Title/Abstract Full Text View citing articles Show Details
T=500°C; 0.0277778 h; Formation of xenobiotics;
14
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Rx-ID: 9121340 Find similar reactions
With hydrogen; 1-n-butyl-3-methylimidazolium tetrafluoroborate; [Ru(η6-p-cymene)(η2-TRIPHOS)Cl][PF6] T=90°C; P=45603.1 Torr; 1 h;
Boxwell, Clive J.; Dyson, Paul J.; Ellis, David J.; Welton, Thomas
Journal of the American Chemical Society, 2002 , vol. 124, # 32 p. 9334 - 9335 Title/Abstract Full Text View citing articles Show Details
15
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Rx-ID: 8644221 Find similar reactions
With potassium hydride in tetrahydrofuran
T=20°C; Elimination; Petersen reaction;
Anderson, James C.; Flaherty, Alice
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 18 p. 3025 - 3027 Title/Abstract Full Text View citing articles Show Details
16
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Rx-ID: 15690949 Find similar reactions
Multi-step reaction with 2 steps 1.1: 9-BBN / tetrahydrofuran 1.2: H2O2; aq. NaOH / tetrahydrofuran; ethanol 2.1: KH / tetrahydrofuran / 20 °C View Scheme
Anderson, James C.; Flaherty, Alice
Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 18 p. 3025 - 3027 Title/Abstract Full Text View citing articles Show Details
17
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Rx-ID: 1615196 Find similar reactions
80%
With zinc; Co-complex 3 in N,N-dimethyl-formamide
T=20°C;
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Giese, Bernd; Erdmann, Peter; Goebel, Thomas; Springer, Ronald
Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4545 - 4548 Title/Abstract Full Text View citing articles Show Details
18
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Rx-ID: 1615198 Find similar reactions
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85%
With zinc; Co-complex 3 in N,N-dimethyl-formamide
T=20°C; other alkyl halides, different allyl compounds; MechanismProduct distribution;
Giese, Bernd; Erdmann, Peter; Goebel, Thomas; Springer, Ronald
Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4545 - 4548 Title/Abstract Full Text View citing articles Show Details
85%
With zinc; Co-complex 3 in N,N-dimethyl-formamide
T=20°C;
Giese, Bernd; Erdmann, Peter; Goebel, Thomas; Springer, Ronald
Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4545 - 4548 Title/Abstract Full Text View citing articles Show Details
19
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Rx-ID: 1615215 Find similar reactions
74%
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Giese, Bernd; Erdmann, Peter; Goebel, Thomas; Springer, Ronald
Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4545 - 4548 Title/Abstract Full Text View citing articles Show Details
With zinc; Co-complex 3 in N,N-dimethyl-formamide
T=20°C;
20
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Rx-ID: 1615216 Find similar reactions
52%
With zinc; Co-complex 3 in N,N-dimethyl-formamide
T=20°C;
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Giese, Bernd; Erdmann, Peter; Goebel, Thomas; Springer, Ronald
Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4545 - 4548
Title/Abstract Full Text View citing articles Show Details
A
B
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21
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Rx-ID: 1615690 Find similar reactions
With tri-n-butyl-tin hydride; 2,2'-azo-bisisobutyronitrile in benzene
T=80°C; Yields of byproduct given;
Curran; Van Elburg
Tetrahedron Letters, 1990 , vol. 31, # 20 p. 2861 - 2864 Title/Abstract Full Text View citing articles Show Details
With tri-n-butyl-tin hydride; 2,2'-azo-bisisobutyronitrile in benzene
T=80°C; Yield given;
Curran; Van Elburg
Tetrahedron Letters, 1990 , vol. 31, # 20 p. 2861 - 2864 Title/Abstract Full Text View citing articles Show Details
22
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Rx-ID: 2212974 Find similar reactions
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Brown, Herbert C.; Rangaishenvi, Milind V.
Tetrahedron Letters, 1990 , vol. 31, # 45 p. 7115 - 7118 Title/Abstract Full Text View citing articles Show Details
Yield given. Multistep reaction;
23
Rx-ID: 1853408
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49 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation; Mechanism;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
49 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
24
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Rx-ID: 1982255 Find similar reactions
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57 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation; Mechanism;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
57 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
25
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Rx-ID: 1986732 Find similar reactions
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42 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation; Mechanism;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
42 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
26
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Rx-ID: 3325357 Find similar reactions
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40 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation; Mechanism;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
40 % Chromat.
in dimethyl sulfoxide
T=35 - 45°C; 24 h; Irradiation;
Russell, Glen A.; Ngoviwatchai, Preecha; Wu, Yuh Wern
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4921 - 4927 Title/Abstract Full Text View citing articles Show Details
27
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Rx-ID: 1650191 Find similar reactions
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Kuchar, Miroslav; Brunova, Bohumila; Grimova, Jaroslava; Vanecek, Stanislav; Holubek, Jiri
Collection of Czechoslovak Chemical Communications, 1986 , vol. 51, # 12 p. 2896 - 2908 Title/Abstract Full Text Show Details
1)dioxane, reflux, 2) water; Yield given. Multistep reaction;
28
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With n-butyllithium in diethyl ether
T=-30 - -25°C;
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Rx-ID: 2811853 Find similar reactions
Villieras, J.; Rambaud, M.; Kirschleger, B.; Tarhouni, R.
Bulletin de la Societe Chimique de France, 1985 , # 5 p. 837 - 843 Title/Abstract Full Text Show Details
29
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Rx-ID: 7242232 Find similar reactions
With 2,2'-azo-bisisobutyronitrile in toluene
T=80°C;
Keck, Gary E.; Enholm, Eric J.; Yates, John B.; Wiley, Michael R.
Tetrahedron, 1985 , vol. 41, # 19 p. 4079 - 4094 Title/Abstract Full Text View citing articles Show Details
30
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Rx-ID: 20753529 Find similar reactions
Multi-step reaction with 2 steps 1: 92.5 percent / HMPA / tetrahydrofuran; diethyl ether; H2O / -100 - -60 °C 2: 76 percent / nBuLi / diethyl ether / -30 - -25 °C View Scheme
Villieras, J.; Rambaud, M.; Kirschleger, B.; Tarhouni, R.
Bulletin de la Societe Chimique de France, 1985 , # 5 p. 837 - 843 Title/Abstract Full Text Show Details
A
B
C
D
E
F
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31
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Rx-ID: 1915238 Find similar reactions
A: 0.7% B: 4.2% C: 200 % D: 0.6% E: 2.5% F: 13%
T=440°C; 0.00111111 h; Heatingother temp.; Product distribution;
Ondruschka, B.; Zimmermann, G.; Anders, G.
Journal fuer Praktische Chemie (Leipzig), 1984 , vol. 326, # 6 p. 853 - 862 Title/Abstract Full Text Show Details
32
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Rx-ID: 1986762 Find similar reactions
22%
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With dilithium tetrachlorocuprate; triphenylphosphine in octane
T=50°C; 5 h;
Dzhemilev, U. M.; Ibragimov, A. G.; Minsker, D. L.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1984 , vol. 33, p. 625 - 627 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1984 , # 3 p. 675 - 677 Title/Abstract Full Text View citing articles Show Details
33
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Rx-ID: 1615229 Find similar reactions
88%
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Keck, Gary E.; Yates, John B.
Journal of the American Chemical Society, 1982 , vol. 104, # 21 p. 5829 - 5831 Title/Abstract Full Text View citing articles Show Details
With 2,2'-azo-bisisobutyronitrile in toluene
T=80°C; 8 h;
34
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Rx-ID: 7242230 Find similar reactions
Korte,W.D. et al.
Journal of Organic Chemistry, 1974 , vol. 39, p. 1168 - 1170 Full Text View citing articles Show Details
Buechi; Wueest
Tetrahedron Letters, 1977 , p. 4305 Full Text Show Details
Pabiot; Pallaud
Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1970 , vol. 271, p. 150 Full Text Show Details
Aso et al.
Kogyo Kagaku Zasshi, 1967 , vol. 70, p. 1001,1002, 1005 Full Text Show Details
Cristol et al.
Journal of the American Chemical Society, 1973 , vol. 95, p. 7067,7068,7069,7072,7073 Full Text View citing articles Show Details
Toptschiew et al.
Doklady Chemistry, 1962 , vol. 147, p. 1064 Doklady Akademii Nauk SSSR, 1962 , vol. 147, p. 857 Full Text Show Details
Gelli et al.
Annali di Chimica (Rome, Italy), 1964 , vol. 54, p. 1143,1146 Full Text Show Details
Schichmamedbekowa et al.
Azerbaidzhanskii Khimicheskii Zhurnal, 1975 , vol. 3, p. 28,32 Chem.Abstr., 1976 , vol. 84, # 89675 Full Text Show Details
35
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Rx-ID: 694357 Find similar reactions
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With diethyl ether
v. Braun; Deutsch; Schmatloch Chemische Berichte, 1912 , vol. 45, p. 1255 Full Text Show Details de Resseguier Bulletin de la Societe Chimique de France, 1910 , vol. <4> 7, p. 433 Full Text Show Details
Beckwith,A.L.J.; Moad,G.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1975 , p. 1726 - 1733 Full Text View citing articles Show Details
36
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Rx-ID: 1231005 Find similar reactions
Multistep reaction;
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Zweifel,G.; Horng,A.
Synthesis, 1973 , p. 672 - 674 Full Text View citing articles Show Details
37
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Rx-ID: 1352880 Find similar reactions
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Benkeser,R.A. et al.
Journal of the American Chemical Society, 1968 , vol. 90, p. 1871 - 1875 Full Text View citing articles Show Details
38
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Rx-ID: 1352798 Find similar reactions
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With di-tert-butyl peroxide
Freidlin,L.Kh. et al.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1967 , p. 1524 - 1528 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1967 , p. 1585 - 1590 Full Text View citing articles Show Details
A
B
C
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39
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T=360°C; P=139746 Torr;
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Mark; Pines
Journal of the American Chemical Society, 1956 , vol. 78, p. 5946,5947 Full Text Show Details
Mark; Pines
Journal of the American Chemical Society, 1956 , vol. 78, p. 5946,5947 Full Text Show Details
T=355°C; P=137540 Torr;
40
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Rx-ID: 7046956 Find similar reactions
Bourguel
Bulletin de la Societe Chimique de France, 1927 , vol. <4> 41, p. 1476 Full Text Show Details
Bourguel
Bulletin de la Societe Chimique de France, 1927 , vol. <4> 41, p. 1447 Bulletin de la Societe Chimique de France, 1928 , vol. <4> 43, p. 231 Full Text Show Details
Kinetics;
41
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Hydrogenation;
Rx-ID: 7242231 Find similar reactions
Bourguel
Bulletin de la Societe Chimique de France, 1927 , vol. <4> 41, p. 1476 Full Text Show Details