4-Methylbenzoic acid (p-Toluic acid)

Page 1

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Reactions (774)

Yield

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Substances (1)

Citations (976)

Conditions

References A

B

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496

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A: 61% B: 95%

497

With lithium amalgam in diethyl ether

Horner, Leopold; Dickerhof, Karlheinz

Chemische Berichte, 1983 , vol. 116, # 4 p. 1615 - 1622 Title/Abstract Full Text Show Details


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Rx-ID: 2827371 Find similar reactions

Drozdova, O. A.; Astrat'ev, A. A.; Kuznetsov, L. L.; Selivanov, V. F.

Journal of Organic Chemistry USSR (English Translation), 1983 , vol. 19, # 4 p. 675 - 680 Zhurnal Organicheskoi Khimii, 1983 , vol. 19, # 4 p. 766 - 771 Title/Abstract Full Text Show Details

With sulfuric acid in water

T=25 - 55.3°C; Dependence of rate on conc. of H2SO4; Rate constantKinetics;

A

B

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498

Synthesize Find similar Rx-ID: 2931246 Find similar reactions

Rodriguez, H.; Pavez, H.; Marquez, A.; Navarrete, P.

Tetrahedron, 1983 , vol. 39, # 1 p. 23 - 27 Title/Abstract Full Text View citing articles Show Details

With sodium hydroxide in methanol

A

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C

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499

Synthesize Find similar Rx-ID: 3156359 Find similar reactions

With tert.-butyl lithium; lithium perchlorate; ammonium chloride

1) THF, pentane, -100 deg C, 2) THF, pentane, r.t.; Yield given. Multistep reaction. Yields of byproduct given;

500

Hellwinkel, Dieter; Laemmerzahl, Frank; Hofmann, Gunter

Chemische Berichte, 1983 , vol. 116, # 10 p. 3375 - 3405 Title/Abstract Full Text Show Details


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Rx-ID: 3537021 Find similar reactions

68%

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With aluminium trichloride

2 h;

Martynov, I. V.; Degtyarev, A. N.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1983 , vol. 32, # 3 p. 588 - 589 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1983 , # 3 p. 650 - 652 Title/Abstract Full Text View citing articles Show Details

501

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Rx-ID: 1937796 Find similar reactions

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With samarium diiodide in tetrahydrofuran

72 h; Ambient temperature;

Souppe, J.; Namy, J. L.; Kagan, H. B.

Tetrahedron Letters, 1982 , vol. 23, # 34 p. 3497 - 3500 Title/Abstract Full Text View citing articles Show Details

A

B

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502

Synthesize Find similar Rx-ID: 2036275 Find similar reactions

With water

T=25°C; MechanismRate constant;

Cox, Robin A.; Yates, Keith

Canadian Journal of Chemistry, 1982 , vol. 60, p. 3061 - 3070 Title/Abstract Full Text Show Details

A

503

B


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With sulfuric acid in water

T=25°C; Mechanism;

Cox, Robin A.; Yates, Keith

Canadian Journal of Chemistry, 1982 , vol. 60, p. 3061 - 3070 Title/Abstract Full Text Show Details

With sulfuric acid in water

T=25°C; Rate constantMechanism;

Cox, Robin A.; Yates, Keith

Canadian Journal of Chemistry, 1982 , vol. 60, p. 3061 - 3070 Title/Abstract Full Text Show Details

A

B

C

D

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504

Synthesize Find similar Rx-ID: 3285602 Find similar reactions

A: 30% B: 15% C: 60% D: 40%

With sodium methylate in methanol

35 deg C -> 20 deg C, 2 h;

Katritzky, Alan R.; Patel, Ranjan C.; Zia, Abid

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1982 , p. 137 - 142 Title/Abstract Full Text View citing articles Show Details

505

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Rx-ID: 7454276 Find similar reactions

With water

T=50°C; Mechanism;

Cox, Robin A.; Yates, Keith

Canadian Journal of Chemistry, 1982 , vol. 60, p. 3061 - 3070 Title/Abstract Full Text Show Details

With sulfuric acid; water

Rate constant;

Cox, Robin A.; Yates, Keith

Canadian Journal of Chemistry, 1982 , vol. 60, p. 3061 - 3070 Title/Abstract Full Text Show Details

A

B

C


506

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A: 12.5% B: 47% C: 26%

With K2S2O8; copper(II) sulfate in acetic acid

T=80 - 85°C; 4 h;

Perumal, P. Thirumalai; Bhatt, M. Vivekananda

Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1981 , vol. 20, # 2 p. 153 - 155 Title/Abstract Full Text Show Details

A: 12.5% B: 47% C: 26%

With K2S2O8; copper(II) sulfate in acetic acid

T=80 - 85°C; 4 h;

Perumal, P. Thirumalai; Bhatt, M. Vivekananda

Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1981 , vol. 20, # 2 p. 153 - 155 Title/Abstract Full Text Show Details

A

B

C

D

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507

Synthesize Find similar Rx-ID: 2005661 Find similar reactions

508

A: 34% B: 8% C: 13% D: 28%

With copper diacetate; anhydrous cobalt diacetate; acetic acid; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A: 34% B: 8% C: 13% D: 28%

With copper diacetate; anhydrous cobalt diacetate; acetic acid; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details


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81%

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Rx-ID: 2064385 Find similar reactions

With sodium hydroxide

1 h;

Olah, George A.; Bruce, Mark R.; Clouet, Francoise L.

Journal of Organic Chemistry, 1981 , vol. 46, # 2 p. 438 - 442 Title/Abstract Full Text View citing articles Show Details

A

B

C

D

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509

Synthesize Find similar Rx-ID: 2068363 Find similar reactions

A: 44% B: 17% C: 16% D: 10%

With copper diacetate; anhydrous cobalt diacetate; acetic acid; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A: 44% B: 17% C: 16% D: 10%

With copper diacetate; anhydrous cobalt diacetate; acetic acid; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A: 44% B: 17% C: 16% D: 10%

With air; copper diacetate; anhydrous cobalt diacetate; acetic acid; sodium bromide

T=150°C; P=30400 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A

B

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510

Synthesize Find similar Rx-ID: 2189098 Find similar reactions

With sodium hydroxide in methanol; water

T=65.5°C; other concentrations of methanol; Rate constant;

Broxton, Trevor J.; Fernando, Denise R.; Rowe, Jeffrey E.

Journal of Organic Chemistry, 1981 , vol. 46, # 17 p. 3522 - 3525 Title/Abstract Full Text View citing articles Show Details

With barium dihydroxide; N-hexadecyl-N,N,N-trimethylammonium bromide in water

T=30°C; dependence of rate constant on concentration of cetyltrimethylammonium bromide; Rate constantMechanism;

Broxton, Trevor J.; Duddy, Neil W.

Australian Journal of Chemistry, 1980 , vol. 33, # 7 p. 1771 - 1781


Title/Abstract Full Text Show Details

A

B

C

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511

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A: 2% B: 6% C: 38%

With potassium superoxide; 18-crown-6 ether in benzene

168 h; Ambient temperature;

Galliani, Guido; Rindone, Bruno

Tetrahedron, 1981 , vol. 37, p. 2313 - 2318 Title/Abstract Full Text View citing articles Show Details

A: 2% B: 6% C: 38%

With potassium superoxide; 18-crown-6 ether in benzene

168 h; Ambient temperature;

Galliani, Guido; Rindone, Bruno

Tetrahedron, 1981 , vol. 37, p. 2313 - 2318 Title/Abstract Full Text View citing articles Show Details

A

B

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512

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Rx-ID: 2258921 Find similar reactions

B: 74%

With palladium diacetate in acetonitrile

P=6619.6 Torr; 0.5 h; Ambient temperature; Yields of byproduct given. Title compound not separated from byproducts;

Kikukawa, Kiyoshi; Kono, Kiyoshi; Nagira, Kazuhiko; Wada, Fumio; Matsuda, Tsutomu

Journal of Organic Chemistry, 1981 , vol. 46, p. 4413 - 4416 Title/Abstract Full Text View citing articles Show Details

A

B

C

D

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513

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Rx-ID: 2392532 Find similar reactions

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Cocco, Maria Teresa; Plumitallo, Antonio; Secci, Mario

Gazzetta Chimica Italiana, 1981 , vol. 111, # 11/12 p. 519 - 520 Title/Abstract Full Text Show Details

With ethylmagnesium bromide

1.) Et2O, 2.) C6H6, 25 h, reflux; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given;

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B

C

D

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514

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Rx-ID: 2880444 Find similar reactions

A: 34% B: 8% C: 13% D: 28%

With copper diacetate; anhydrous cobalt diacetate; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A: 34% B: 8% C: 13% D: 28%

With air; copper diacetate; anhydrous cobalt diacetate; sodium bromide

T=150°C; P=30400 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A

B

C

D

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515

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Rx-ID: 2880445 Find similar reactions

A: 34% B: 4% C: 13% D: 28%

With copper diacetate; anhydrous cobalt diacetate; sodium bromide

T=150°C; P=29420.3 Torr; 1 h; Further byproducts given;

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

A

B

C

D


516

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Rx-ID: 2880737 Find similar reactions

A: 44% B: 17% C: 16% D: 10%

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With air; copper diacetate; anhydrous cobalt diacetate; sodium bromide

T=150°C; P=30400 Torr; 1 h; Further byproducts given;

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Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

517

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20%

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Rx-ID: 3042477 Find similar reactions

Ranganathan, D.; Ranganathan, S.; Rao, C. B.

Tetrahedron, 1981 , vol. 37, p. 637 - 641 Title/Abstract Full Text View citing articles Show Details

in xylene

Heating; MechanismProduct distribution;

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B

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518

Synthesize Find similar Rx-ID: 3278464 Find similar reactions

A: 60% B: 65%

Oida, Tatsuo; Shimizu, Tomio; Hayashi, Yoshiyuki; Teramura, Kazuhiro

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 5 p. 1429 - 1433 Title/Abstract Full Text Show Details

T=200°C; 0.166667 h;

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B

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519

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Rx-ID: 3917723 Find similar reactions

A: 0.734 % Turnov. B: 0.910 % Turnov.

With iron(III) benzoate

T=80°C; without reagent;

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Bolton, Roger; Dailly, Bryce N.; Hirakubo, Kazuko; Lee, Kong Hung; Williams, Gareth H.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1981 , p. 1109 - 1120 Title/Abstract Full Text View citing articles Show Details

520

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Rx-ID: 19400196 Find similar reactions

Multi-step reaction with 2 steps 1: 34 percent / cobalt(II) acetate, copper(II) acetate, sodium bromide, acetic acid / 1 h / 150 °C / 29420.3 Torr 2: 10 percent / cobalt(II) acetate, copper(II) acetate, sodium bromide, acetic acid, air / 1 h / 150 °C / 30400 Torr View Scheme

Okada, Toshihiko; Kamiya, Yoshio

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2724 - 2727 Title/Abstract Full Text Show Details

521

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Multi-step reaction with 2 steps 1: 70 percent / triethylamine / benzene / 48 h 2: 60 percent / 0.17 h / 200 °C View Scheme

A

Rx-ID: 19406568 Find similar reactions

Oida, Tatsuo; Shimizu, Tomio; Hayashi, Yoshiyuki; Teramura, Kazuhiro

Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 5 p. 1429 - 1433 Title/Abstract Full Text Show Details

B


522

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Rx-ID: 25002599 Find similar reactions

Mitsubishi Gas Chemical Company, Inc.

Patent: US4255592 A1, 1981 ;

Hide Experimental Procedure

Title/Abstract Full Text Show Details

C.1:COMPARATIVE EXAMPLE 1

COMPARATIVE EXAMPLE 1 Oxidation was carried out in the same manner as in Example 1, except that 100 g of D-t-BPO (purity: 98percent) was used in place of the t-BHPO solution, whereby 302.2 g of reaction product solution was obtained. As a result of analysis, it was found that p-xylene consumed amounted to 19.7 g, PX-HPO formed 12.1 g, p-tolualdehyde formed 2.4 g, p-methylbenzyl alcohol formed 0.8 g, and p-toluic acid formed 1.51 g.

523

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Rx-ID: 2002613 Find similar reactions

84%

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With sodium acetate; palladium diacetate in acetonitrile

P=6619.6 Torr; 1 h; Ambient temperature;

Nagira, Kazuhiko; Kikukawa, Kiyoshi; Wada, Fumio; Matsuda, Tsutomu

Journal of Organic Chemistry, 1980 , vol. 45, # 12 p. 2365 - 2368 Title/Abstract Full Text View citing articles Show Details

A

B

C

D

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524

Synthesize Find similar Rx-ID: 2007983 Find similar reactions

A: 5.1 % Chromat.

With oxygen; cobalt(II) dibromide in acetic acid

T=140°C; P=7500.6 Torr; 2.41667 h; other time, other catalysator; Product distribution;

Hronec, Milan; Holotik, Stefan; Ilavsky, Jan

Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 3 p. 880 - 887


B: 26.9 % Chromat. C: 42.7 % Chromat. D: 0.8 % Chromat.

Title/Abstract Full Text Show Details

A

B

C

D

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525

Synthesize Find similar Rx-ID: 2008507 Find similar reactions

A: 7.8 % Chromat. B: 1.4 % Chromat. C: 50.2 % Chromat. D: 3.1 % Chromat.

Hronec, Milan; Holotik, Stefan; Ilavsky, Jan

Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 3 p. 880 - 887 Title/Abstract Full Text Show Details

With oxygen; MnBr2(pyridine)2; dibromobis(pyridine)cobalt(II) in acetic acid

T=140°C; P=7500.6 Torr; 1 h; other time; Product distribution;

A

B

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526

Synthesize Find similar Rx-ID: 2187249 Find similar reactions

With barium dihydroxide; N-hexadecyl-N,N,N-trimethylammonium bromide in water

T=30°C; dependence of rate constant on concentration of cetyltrimethylammonium bromide; Rate constantMechanism;

Broxton, Trevor J.; Duddy, Neil W.

Australian Journal of Chemistry, 1980 , vol. 33, # 7 p. 1771 - 1781 Title/Abstract Full Text Show Details

A

B


527

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Rx-ID: 2392945 Find similar reactions

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With potassium hydride

1) THF, 20-30 deg C, 1 h; 2) THF, 1 h; Yield given. Multistep reaction. Yields of byproduct given;

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Rathman, Terry L.; Greenwood, Thomas D.; Wolfe, James F.

Journal of Organic Chemistry, 1980 , vol. 45, # 6 p. 1086 - 1091 Title/Abstract Full Text View citing articles Show Details

A

B

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528

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Rx-ID: 2723382 Find similar reactions

A: 40% B: 14%

in N,N-dimethyl acetamide

16 h; Ambient temperature;

Harada; Kaji; Zen

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 11 p. 3296 - 3303 Title/Abstract Full Text View citing articles Show Details

A: 40% B: 14%

in N,N-dimethyl acetamide

16 h; Ambient temperature;

Harada; Kaji; Zen

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 11 p. 3296 - 3303 Title/Abstract Full Text View citing articles Show Details

529

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89%

With W-7 Raney-Nickel in ethanol

5 h; Heating;

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Rx-ID: 2731011 Find similar reactions

Mitchell, Reginald H.; Lai, Yee-Hing

Tetrahedron Letters, 1980 , vol. 21, # 27 p. 2637 - 2638 Title/Abstract Full Text View citing articles Show Details


A

B

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530

Synthesize Find similar Rx-ID: 2985331 Find similar reactions

A: 64% B: 66%

With sodium hydroxide

1.25 h; Heating;

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

A

B

C

D

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531

Synthesize Find similar Rx-ID: 2985352 Find similar reactions

A: 35% B: 12% C: 10% D: 16%

in acetonitrile

38 h; Irradiation;

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

A: 35% B: 12% C: 10% D: 16%

in acetonitrile

38 h; Irradiation;

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

A

532

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B


Find similar Rx-ID: 2985362 Find similar reactions

A: 70% B: 69%

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With sodium hydroxide

Heating;

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

A

B

C

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533

Synthesize Find similar Rx-ID: 3050758 Find similar reactions

A: 73% B: 30% C: 59%

With antimony(V) pentachloride in dichloromethane

T=20°C; 90 h;

Miura, Masahiro; Nojima, Masamoto; Kusabayashi, Shigekazu

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 1950 - 1954 Title/Abstract Full Text View citing articles Show Details

A: 73% B: 30% C: 59%

With antimony(V) pentachloride in dichloromethane

T=20°C; 90 h;

Miura, Masahiro; Nojima, Masamoto; Kusabayashi, Shigekazu

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 1950 - 1954 Title/Abstract Full Text View citing articles Show Details

A: 73% B: 30% C: 59%

With antimony(V) pentachloride in dichloromethane

T=20°C; 1.5 h; other reagent, time; Product distribution;

Miura, Masahiro; Nojima, Masamoto; Kusabayashi, Shigekazu

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 1950 - 1954 Title/Abstract Full Text View citing articles Show Details

A

B

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534

Synthesize Find similar Rx-ID: 3424367 Find similar reactions

A: 14% B: 86%

A: 14% B: 86%

With copper diacetate; oxygen

With copper diacetate; oxygen

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Tsuji, Jiro; Nagashima, Toshiharu; Qui, Nguyen Thi; Takayanagi, Hiroshi

Tetrahedron, 1980 , vol. 36, p. 1311 - 1315 Title/Abstract Full Text View citing articles Show Details

Tsuji, Jiro; Nagashima, Toshiharu; Qui, Nguyen Thi; Takayanagi, Hiroshi

Tetrahedron, 1980 , vol. 36, p. 1311 - 1315 Title/Abstract Full Text View citing articles Show Details


535

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Rx-ID: 20560613 Find similar reactions

Multi-step reaction with 2 steps 1: 95 percent / acetonitrile / 20 °C 2: 12 percent / acetonitrile / 38 h / Irradiation View Scheme

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

Multi-step reaction with 3 steps 1: 95 percent / acetonitrile / 20 °C 2: 10 percent / acetonitrile / 38 h / Irradiation 3: 66 percent / 20percent NaOH / 1.25 h / Heating View Scheme

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

Multi-step reaction with 3 steps 1: 95 percent / acetonitrile / 20 °C 2: 16 percent / acetonitrile / 38 h / Irradiation 3: 69 percent / 20percent NaOH / Heating View Scheme

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

536

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Rx-ID: 20570266 Find similar reactions

Multi-step reaction with 2 steps 1: 10 percent / acetonitrile / 38 h / Irradiation 2: 66 percent / 20percent NaOH / 1.25 h / Heating View Scheme

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details

Multi-step reaction with 2 steps 1: 16 percent / acetonitrile / 38 h / Irradiation 2: 69 percent / 20percent NaOH / Heating View Scheme

Katritzky, Alan R.; Chapman, Andrew V.; Cook, Michael J.; Millet, George H.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2743 - 2754 Title/Abstract Full Text View citing articles Show Details


537

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Rx-ID: 4047038 Find similar reactions

With sodium hydroxide; silver nitrate in water

Wiemann,J.; Dupayrat,J.

Bulletin de la Societe Chimique de France, 1961 , p. 757 Full Text View citing articles Show Details

A

B

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538

Synthesize Find similar Rx-ID: 7059552 Find similar reactions

Manukowskaja et al.

Zhurnal Obshchei Khimii, 1959 , vol. 29, p. 158; engl. Ausg. S. 162 Full Text View citing articles Show Details

T=135°C;

A

B

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539

Synthesize Find similar Rx-ID: 7059553 Find similar reactions

T=330 - 400°C; Oxydation;

Suworow et al.

Izv. Akad. Kazachsk. S. S. R. Ser. chim.Chem.Abstr., 1959 , # 1 p. 80 Izv. Akad. Kazachsk. S. S. R. Ser. chim.Chem.Abstr., 1961 , p. 2563 Full Text Show Details


540

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Rx-ID: 8255514 Find similar reactions

Miklaschewskaja; Petrow

Zhurnal Obshchei Khimii, 1958 , vol. 28, p. 1125; engl. Ausg. S. 1187 Full Text Show Details

A

B

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541

Synthesize Find similar Rx-ID: 662152 Find similar reactions

With nitric acid

Nasarow; Semenowskii

Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1956 , p. 1487,1490; engl. Ausg. S. 1529, 1531 Full Text View citing articles Show Details

Akiyoshi et al.

Technol. Rep. Kyushu Univ.Chem.Abstr., 1951 , vol. 24, p. 16,19 Technol. Rep. Kyushu Univ.Chem.Abstr., 1953 , p. 4867 Full Text Show Details

542

Synthesize Find similar

Synthesize Find similar

Rx-ID: 750444 Find similar reactions

With acetic acid; zinc(II) chloride; trichlorophosphate

T=105 - 110°C; Behandeln des Reaktionsprodukts mit Wasser;

Frey; Horowitz

Journal fuer Praktische Chemie (Leipzig), 1891 , vol. <2> 43, p. 114 Full Text View citing articles Show Details

Multi-step reaction with 2 steps

Gattermann; Schmidt


1: AlCl3

2: alkaline solution View Scheme

Justus Liebigs Annalen der Chemie, 1888 , vol. 244, p. 52 Chemische Berichte, 1887 , vol. 20, p. 860 Full Text Show Details

Multi-step reaction with 2 steps 1: zinc chloride; hydrogen chloride 2: aqueous HNO3

View Scheme

Nasarow; Semenowskii

Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1956 , p. 1487,1490; engl. Ausg. S. 1529, 1531 Full Text View citing articles Show Details

Hide Details

Multi-step reaction with 2 steps 1: aluminium chloride; hydrogen chloride / Zersetzen des Reaktionsprodukts mit Eis 2: diluted NaOH-solution View Scheme

Houben; Fischer

Journal fuer Praktische Chemie (Leipzig), 1929 , vol. <2> 123, p. 319 Chemische Berichte, 1933 , vol. 66, p. 341 Full Text View citing articles Show Details

543

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059539 Find similar reactions

Ogata et al.

Kogyo Kagaku Zasshi, 1956 , vol. 59, p. 1156 Chem.Abstr., 1958 , p. 14564 Full Text View citing articles Show Details

T=150°C; P=2574.3 Torr;

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

544

Synthesize Find similar Rx-ID: 7061775 Find similar reactions

Kobayashi et al.

Kogyo Kagaku Zasshi, 1956 , vol. 59, p. 654 Chem.Abstr., 1958 , p. 5334 Full Text View citing articles Show Details


545

Synthesize Find similar

Rx-ID: 5855661 Find similar reactions

With sulfuric acid

Babajan

Doklady Akademii Nauk Armyanskoi SSR, 1955 , vol. 21, p. 77 Chem.Abstr., 1956 , p. 5571 Full Text Show Details

546

Synthesize Find similar

Synthesize Find similar

Rx-ID: 6219081 Find similar reactions

With boron trifluoride; acetic acid

T=115 - 120°C; Behandeln des Reaktionsgemisches mit wss. NaOH;

Hauser; Hoffenberg

Journal of Organic Chemistry, 1955 , vol. 20, p. 1448,1449 Full Text Show Details

547

Synthesize Find similar

Rx-ID: 7059531 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Babajan

Doklady Akademii Nauk Armyanskoi SSR, 1955 , vol. 21, p. 77 Chem.Abstr., 1956 , p. 5571 Full Text Show Details

2-taegiges Erwaermen;

A

B

C


548

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059568 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Cullis; Ladbury

Journal of the Chemical Society, 1955 , p. 1407,1411 Full Text View citing articles Show Details

T=50°C; Kinetics;

A

B

C

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Synthesize Find similar

Synthesize Find similar

549

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059569 Find similar reactions

Cullis; Ladbury

Journal of the Chemical Society, 1955 , p. 2850,2854 Full Text Show Details

T=50°C; Kinetics;

A

B

Synthesize Find similar

Synthesize Find similar

550

Synthesize Find similar Rx-ID: 7061770 Find similar reactions

T=170°C;

Chmura et al.

Zhurnal Obshchei Khimii, 1955 , vol. 25, p. 1418,1422; engl. Ausg. S. 1363, 1366 Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

551

Synthesize Find similar Rx-ID: 7061771 Find similar reactions

Chmura et al.

Zhurnal Obshchei Khimii, 1955 , vol. 25, p. 1418,1422; engl. Ausg. S. 1363, 1366 Full Text View citing articles Show Details

T=170°C;

A

B

Synthesize Find similar

Synthesize Find similar

552

Synthesize Find similar Rx-ID: 7061772 Find similar reactions

Chmura et al.

Zhurnal Obshchei Khimii, 1955 , vol. 25, p. 1418,1422; engl. Ausg. S. 1363, 1366 Full Text View citing articles Show Details

T=170°C;

A

B

Synthesize Find similar

Synthesize Find similar

553

Synthesize Find similar Rx-ID: 7061773 Find similar reactions

T=170°C;

Chmura et al.

Zhurnal Obshchei Khimii, 1955 , vol. 25, p. 1418,1422; engl. Ausg. S. 1363, 1366 Full Text View citing articles Show Details


554

Synthesize Find similar

Rx-ID: 7458551 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Lynch; Pausacker

Journal of the Chemical Society, 1955 , p. 1525,1528 Full Text View citing articles Show Details

T=25°C; sowie bei 30grad, 35grad und 40grad; Rate constant;

555

Synthesize Find similar

Synthesize Find similar

Rx-ID: 404696 Find similar reactions

With sulfuric acid

T=140°C;

DEGUSSA

Patent: DE963331 , 1954 ; Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

556

Synthesize Find similar Rx-ID: 7059549 Find similar reactions

Synthesize Find similar

Yen

Chlorine Alkali NewsChem.Abstr., 1953 , # 11 p. 44 Chlorine Alkali NewsChem.Abstr., 1955 , p. 7523 Full Text Show Details

Product distribution;

A

B

C


557

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059558 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Yen

Chlorine Alkali NewsChem.Abstr., 1953 , # 11 p. 44 Chlorine Alkali NewsChem.Abstr., 1955 , p. 7523 Full Text Show Details

Erhitzen des Reaktionsprodukts mit wss. Salpetersaeure;

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

558

Synthesize Find similar Rx-ID: 8262348 Find similar reactions

Suworow; Rafikow

Izv. Akad. Kazachsk. S.S.R. Ser. chim.Chem.Abstr., 1953 , # 7 p. 70 Izv. Akad. Kazachsk. S.S.R. Ser. chim.Chem.Abstr., 1955 , p. 2422 Full Text Show Details

559

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5855672 Find similar reactions

Codington; Mosettig

Journal of Organic Chemistry, 1952 , vol. 17, p. 1035,1040 Full Text View citing articles Show Details

With pyridine

T=195°C; Erhitzen des Reaktionsgemisches mit wss. H2SO4 auf 150grad;

A

B


560

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26837989 Find similar reactions

A: 7-8 B: 26-30

Synthesize Find similar

With n-butyllithium in diethyl ether

after carbonylation and hydrolysis;

Gilman; Yale

Journal of the American Chemical Society, 1950 , vol. 72, p. 8 Full Text View citing articles Show Details

Gmelin Handbook: Bi: Org.Verb., 1.3.3.2.7, page 92 - 93 Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

561

Synthesize Find similar

Synthesize Find similar

Rx-ID: 749579 Find similar reactions

With carbon disulfide; aluminium trichloride

Fahim

Journal of the Chemical Society, 1949 , p. 520 Full Text View citing articles Show Details

562

Synthesize Find similar

Rx-ID: 825713 Find similar reactions

Synthesize Find similar

With oxygen; anhydrous cobalt diacetate; Neutral lead acetate

T=140 - 145°C; weiteres Reagens: Mangan(II)-acetat;

Synthesize Find similar

Emerson; Lucas; Heimsch

Journal of the American Chemical Society, 1949 , vol. 71, p. 1742 Full Text View citing articles Show Details


563

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5855670 Find similar reactions

With dicobalt octacarbonyl; benzene

T=300°C; P=441305 Torr;

Du Pont de Nemours and Co.

Patent: US2565461 , 1949 ;

With hydrogenchloride; pentacarbonyliron(0); toluene

T=300°C; P=441305 Torr;

Du Pont de Nemours and Co.

Patent: US2565461 , 1949 ;

Full Text Show Details

Full Text Show Details

564

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5855677 Find similar reactions

With acetic acid

T=300°C; P=220652 Torr;

Du Pont de Nemours and Co.

Patent: US2565463 , 1949 ; Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

565

Synthesize Find similar Rx-ID: 5855685 Find similar reactions

T=20°C;

Synthesize Find similar

Synthesize Find similar

Fahim


Journal of the Chemical Society, 1949 , p. 520 Full Text View citing articles Show Details

Fahim

Nature (London, United Kingdom), 1948 , vol. 162, p. 526 Journal of the Chemical Society, 1949 , p. 520 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

566

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059551 Find similar reactions

Emerson; Lucas; Heimsch

Journal of the American Chemical Society, 1949 , vol. 71, p. 1742 Full Text View citing articles Show Details

T=140 - 145°C; weitere Verbindung: Mangan(II)-acetat;

567

Synthesize Find similar

Synthesize Find similar

Rx-ID: 8255513 Find similar reactions

Kroehnke

Chemische Berichte, 1949 , vol. 66, p. 441,468 Full Text View citing articles Show Details

568

Synthesize Find similar

Rx-ID: 639670 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar


Hauser; Swamer; Ringler

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

T=38°C;

569

Synthesize Find similar

Rx-ID: 5678918 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Kruber; Rappen

Chemische Berichte, 1948 , vol. 81, p. 483,486 Full Text View citing articles Show Details

T=250°C;

A

B

Synthesize Find similar

Synthesize Find similar

570

Synthesize Find similar Rx-ID: 7059573 Find similar reactions

Wichterle; Prochazka; Hofman

Collection of Czechoslovak Chemical Communications, 1948 , vol. 13, p. 300,309 Full Text View citing articles Show Details

571

Synthesize Find similar

Rx-ID: 7918094 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Wichterle; Prochazka; Hofman


Collection of Czechoslovak Chemical Communications, 1948 , vol. 13, p. 300,309 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

572

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059560 Find similar reactions

Ssultanow; Rodionow; Schemjakin

Zhurnal Obshchei Khimii, 1946 , vol. 16, p. 2072,2075 Chem.Abstr., 1948 , p. 881 Full Text View citing articles Show Details

T=250°C;

573

Synthesize Find similar

Rx-ID: 5855689 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Fuson et al.

Journal of Organic Chemistry, 1945 , vol. 10, p. 121,125 Full Text View citing articles Show Details

574

Synthesize Find similar

Rx-ID: 5855692 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Fuson et al.


Journal of Organic Chemistry, 1945 , vol. 10, p. 121,125 Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

575

Synthesize Find similar Rx-ID: 8255522 Find similar reactions

Iwanow; Iwanow

Chemische Berichte, 1944 , vol. 77/79, p. 173 Full Text View citing articles Show Details

Fedoseew

Zhurnal Obshchei Khimii, 1937 , vol. 7, p. 1364 Chem. Zentralbl., 1938 , vol. 109, # I p. 585 Full Text View citing articles Show Details

T=275 - 285°C;

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

576

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 638900 Find similar reactions

Iwanow; Iwanow

Chemische Berichte, 1943 , vol. 76, p. 1148,1154 Chemische Berichte, 1944 , vol. 77/79, p. 173,179 Full Text Show Details

unter Luftzutritt;

A

B

Synthesize

Synthesize

577

Synthesize

Synthesize

Synthesize


Find similar

Find similar

Find similar

Rx-ID: 8259742 Find similar reactions

Find similar

Find similar

Iwanow; Iwanow

Chemische Berichte, 1943 , vol. 76, p. 1148,1154 Chemische Berichte, 1944 , vol. 77/79, p. 173,179 Full Text Show Details

unter Luftzutritt;

A

B

Synthesize Find similar

Synthesize Find similar

578

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 8259743 Find similar reactions

Iwanow; Iwanow

Chemische Berichte, 1943 , vol. 76, p. 1148,1154 Chemische Berichte, 1944 , vol. 77/79, p. 173,179 Full Text Show Details

unter Luftzutritt;

A

B

Synthesize Find similar

Synthesize Find similar

579

Synthesize Find similar Rx-ID: 5678922 Find similar reactions

Tommila

Annales Academiae Scientiarum Fennicae, Series A, 1942 , vol. 59, # 4 p. 3,4 Chem.Abstr., 1944 , p. 6173 Full Text View citing articles Show Details

T=40 - 129°C; Disproportionierung; Kinetics;

A

580

B

C


Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059566 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Farmer; Narracott

Journal of the Chemical Society, 1942 , p. 185 Full Text View citing articles Show Details

T=75°C;

A

B

Synthesize Find similar

Synthesize Find similar

581

Synthesize Find similar Rx-ID: 7449938 Find similar reactions

Ishimura

Bulletin of the Chemical Society of Japan, 1941 , vol. 16, p. 252,258 Bulletin of the Chemical Society of Japan, 1943 , vol. 18, p. 200 Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

582

Synthesize Find similar Rx-ID: 8265275 Find similar reactions

T=300 - 350°C;

Synthesize Find similar

Ishimura

Bulletin of the Chemical Society of Japan, 1941 , vol. 16, p. 196,199, 203, 254 Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

583

Synthesize Find similar Rx-ID: 278220 Find similar reactions

With diethyl ether; lithium

Behandeln des Reaktionsgemisches mit festem Kohlendioxid;

Gilman; Langham; Jacoby

Journal of the American Chemical Society, 1939 , vol. 61, p. 106,108 Full Text Show Details

With n-butyllithium; diethyl ether

Behandeln des Reaktionsgemisches mit festem Kohlendioxid;

Gilman; Langham; Moore

Journal of the American Chemical Society, 1940 , vol. 62, p. 2327,2333 Full Text View citing articles Show Details

With n-butyllithium; Petroleum ether

Behandeln des Reaktionsgemisches mit festem Kohlendioxid;

Gilman; Langham; Moore

Journal of the American Chemical Society, 1940 , vol. 62, p. 2327,2333 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

584

Synthesize Find similar Rx-ID: 278248 Find similar reactions

With n-butyllithium; diethyl ether

Behandeln des Reaktionsgemisches mit festem Kohlendioxid;

Gilman; Langham; Moore

Journal of the American Chemical Society, 1940 , vol. 62, p. 2327,2333 Full Text View citing articles Show Details

With n-butyllithium; Petroleum ether

Behandeln des Reaktionsgemisches mit festem Kohlendioxid;

Gilman; Langham; Moore

Journal of the American Chemical Society, 1940 , vol. 62, p. 2327,2333 Full Text View citing articles Show Details


585

Synthesize Find similar

Rx-ID: 7059533 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Zukerwanik; Terent'ewa

Zhurnal Obshchei Khimii, 1940 , vol. 10, p. 1405,1407 Chem. Zentralbl., 1942 , vol. 113, # II p. 1899 Full Text Show Details

586

Synthesize Find similar

Synthesize Find similar

Rx-ID: 7059541 Find similar reactions

Farbenfabr. Bayer

Patent: DE767366 , 1940 ; DRP/DRBP Org.Chem. Full Text Show Details

T=130°C;

587

Synthesize Find similar

Rx-ID: 7059546 Find similar reactions

T=35 - 40°C; Leiten von CO2 in das Reaktionsgemisch;

Synthesize Find similar

Synthesize Find similar

Morton; Le Fevre; Hechenbleikner

Journal of the American Chemical Society, 1936 , vol. 58, p. 754 Full Text View citing articles Show Details

Gilman; Pacevitz; Baine

Journal of the American Chemical Society, 1940 , vol. 62, p. 1514,1519 Full Text View citing articles Show Details

Morton; Stevens

Journal of the American Chemical Society, 1931 , vol. 53, p. 4028,4031


Full Text View citing articles Show Details

Ziegler

Angewandte Chemie, 1936 , vol. 49, p. 455,457 Full Text View citing articles Show Details

588

Synthesize Find similar

Rx-ID: 7059547 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Morton; Le Fevre; Hechenbleikner

Journal of the American Chemical Society, 1936 , vol. 58, p. 754 Full Text View citing articles Show Details

Gilman; Pacevitz; Baine

Journal of the American Chemical Society, 1940 , vol. 62, p. 1514,1519 Full Text View citing articles Show Details

Morton; Stevens

Journal of the American Chemical Society, 1931 , vol. 53, p. 4028,4031 Full Text View citing articles Show Details

Ziegler

Angewandte Chemie, 1936 , vol. 49, p. 455,457 Full Text View citing articles Show Details

T=35 - 40°C; Leiten von CO2 in das Reaktionsgemisch;

589

Synthesize Find similar

T=35 - 40°C; Leiten von CO2 in das Reaktionsgemisch;

Synthesize Find similar

Rx-ID: 7059548 Find similar reactions

Morton; Le Fevre; Hechenbleikner

Journal of the American Chemical Society, 1936 , vol. 58, p. 754 Full Text View citing articles Show Details

Gilman; Pacevitz; Baine

Journal of the American Chemical Society, 1940 , vol. 62, p. 1514,1519 Full Text View citing articles Show Details

Morton; Stevens

Journal of the American Chemical Society, 1931 , vol. 53, p. 4028,4031 Full Text View citing articles Show Details

Ziegler

Angewandte Chemie, 1936 , vol. 49, p. 455,457 Full Text View citing articles Show Details


590

Synthesize Find similar

Rx-ID: 7445141 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Noelting

Chimie et Industrie (Paris), vol. 6, p. 732 Chem. Zentralbl., 1922 , vol. 93, # II p. 750 Full Text View citing articles Show Details

Zukerwanik; Terent'ewa

Zhurnal Obshchei Khimii, 1940 , vol. 10, p. 1405,1407 Chem. Zentralbl., 1942 , vol. 113, # II p. 1899 Full Text Show Details

591

Synthesize Find similar

Rx-ID: 8255508 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Yuan; Hua

Journal of the Chinese Chemical Society (Peking), 1940 , vol. 7, p. 76,98 Full Text Show Details

Erwaermen des Reaktionsprodukts mit wss. Kalilauge;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

592

Synthesize Find similar Rx-ID: 266935 Find similar reactions

Synthesize Find similar

Behaghel; Ratz

Chemische Berichte, 1939 , vol. 72, p. 1257,1269


Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

593

Synthesize Find similar

Synthesize Find similar

Rx-ID: 266937 Find similar reactions

Behaghel; Ratz

Chemische Berichte, 1939 , vol. 72, p. 1257,1269 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

594

Synthesize Find similar Rx-ID: 5855687 Find similar reactions

T=200 - 240°C;

Synthesize Find similar

Lock; Schreckeneder

Chemische Berichte, 1939 , vol. 72, p. 511,515 Full Text View citing articles Show Details


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