Phenylmethanol (BnOH) to Benzaldehyde

Page 1

Bioactivities (22175)

Yield

Reactions (435)

Substances (517)

Targets (1261)

Citations (2617)

Conditions

References A

B

Synthesize Find similar

Synthesize Find similar

298

Synthesize Find similar Rx-ID: 26906653

Find similar reactions

Synthesize Find similar

A: >99

in dichloromethane

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A: >99

With NaNO3/HNO3 buffer in water

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2, pH = 2.00; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A

299

B


Synthesize Find similar

Synthesize Find similar

Rx-ID: 26906654

Find similar reactions

Synthesize Find similar

Synthesize Find similar

A: >99

in dichloromethane

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A: >99

With NaNO3/HNO3 buffer in water

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2, pH = 2.00; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

300

Synthesize Find similar Rx-ID: 26906655

Find similar reactions

Synthesize Find similar

A: >99

in dichloromethane

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A: >99

With NaNO3/HNO3 buffer in water

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2, pH = 2.00; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A

301

B


Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26906656

Find similar reactions

Synthesize Find similar

A: >99

in dichloromethane

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

A: >99

With NaNO3/HNO3 buffer in water

Kinetics; ratio Ru-complex : alc.= 1 : 50, at 25°C under N2, pH = 2.00; sepn. by gas chromy. (FID), yield of benzaldehyde 80-95 percent;

Muller, James G.; Acquaye, John Henry; Takeuchi, Kenneth J.

Inorganic Chemistry, 1992 , vol. 31, p. 4552 - 4557 Full Text View citing articles Show Details

302

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2063920

Find similar reactions

With lt;Ru(VI)(dmbipy)2O2gt;lt;ClO4gt;2 in acetonitrile

T=298°C; 4 h; Rate constant;

Che, Chi-Ming; Leung, Wai-Ho; Li, Chi-Keung; Poon, Chung-Kwong

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1991 , # 3 p. 379 - 384 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

303

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2897155

Find similar reactions

A: 92% B: 3%

With N,N,N,N,N,N-hexamethylphosphoric triamide; bromine; sodium hydrogencarbonate in dichloromethane; water

A

Al Neirabeyeh, Mamdouh; Pujol, M. Dolors

Tetrahedron Letters, 1990 , vol. 31, # 16 p. 2273 - 2276 Title/Abstract Full Text View citing articles Show Details

B

C

D

E

F


304

Synthesize Find similar Rx-ID: 3840154

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

With hydrogen; iron(II,III) oxide; vanadia

T=250°C; P=405.03 Torr; Product distribution;

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Glebov, L. S.; Shuikin, A. N.; Kliger, G. A.; Mikaya, A. I.; Zaikin, V. G.; et al.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1990 , vol. 39, # 4.2 p. 814 - 817 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1990 , # 4 p. 907 - 910 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

305

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26812563

Find similar reactions

A: 0% B: 0%

Lee, Gyu-Hwan; Larson, James L.; Perkins, Thomas A.; Schanze, Kirk S.

Inorganic Chemistry, 1990 , vol. 29, p. 2015 - 2017 Full Text View citing articles Show Details

in benzyl alcohol

Irradiation (UV/VIS); photolysis of Co-complex in benzylalcohol; HPLC;

A

B

Synthesize Find similar

Synthesize Find similar

306

Synthesize Find similar Rx-ID: 3838530

Find similar reactions

B: 68%

in acetonitrile

T=17°C; Irradiation;

Synthesize Find similar

Sulpizio, Ada; Albini, Angelo; d'Alessandro, Nicola; Fasani, Elisa; Pietra, Silvio

Journal of the American Chemical Society, 1989 , vol. 111, # 15 p. 5773 - 5777 Title/Abstract Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

307

Synthesize Find similar Rx-ID: 3840155

Find similar reactions

With 7,8-dimethyl-10-(tetra-O-acetyl-D-arabinitol-1-yl)-10H-benzo[g]pteridine-2,4-dione; perchloric acid in acetonitrile

T=24.9°C; Irradiation;

Fukuzumi, Shunichi; Tanii, Kumiko; Tanaka, Toshio

Chemistry Letters, 1989 , p. 35 - 38 Title/Abstract Full Text Show Details

A

B

C

D

E

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

308

Synthesize Find similar Rx-ID: 3840157

Find similar reactions

Hansen, Sissel H.; Sydnes, Leiv K.

Acta Chemica Scandinavica, 1989 , vol. 43, # 4 p. 395 - 398 Title/Abstract Full Text Show Details

T=20°C; 12 h; Irradiationeffect of irradiation time; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

309

Synthesize Find similar Rx-ID: 26374791

Find similar reactions

A: 4% B: 75%

Synthesize Find similar

With dimethyl terephthalate in chlorobenzene

in a thickwall glass ampule, after filled with the substances evacuated, filled with argon three times, sealed under vacuum, shaked in a oil bath at 150°C for 17 h, cooled; gas chromatography;

Sumner, Charles E. Jr.; Steinmetz, Guy R.

Inorganic Chemistry, 1989 , vol. 28, p. 4290 - 4294 Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

310

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26381898

Find similar reactions

A: 4% B: 82%

With dimethyl terephthalate in chlorobenzene

in a thickwall glass ampule, after filled with the substances evacuated, filled with argon three times, sealed under vacuum, shaked in a oil bath at 150°C for 17 h, cooled; gas chromatography;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Sumner, Charles E. Jr.; Steinmetz, Guy R.

Inorganic Chemistry, 1989 , vol. 28, p. 4290 - 4294 Full Text View citing articles Show Details

311

Synthesize Find similar Rx-ID: 30673672

Find similar reactions

Multi-step reaction with 2 steps 1: acetonitrile 2: dimethyl terephthalate / chlorobenzene View Scheme

Sumner, Charles E. Jr.; Steinmetz, Guy R.

Inorganic Chemistry, 1989 , vol. 28, p. 4290 - 4294 Full Text View citing articles Show Details

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

312

Synthesize Find similar Rx-ID: 1736027

Find similar reactions

Synthesize Find similar


Brown, Jonathan W.; Clack, Dennis W.; Wilson, David A.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1988 , p. 117 - 122 Title/Abstract Full Text View citing articles Show Details

T=200°C; 3 h; Further byproducts given;

A

B

C

D

E

F

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

313

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3298733

Find similar reactions

With sodium hydroxide in water

T=75 - 80°C; catalytically active organic phase analysis; Product distribution;

Shavanov, S. S.; Tolstikov, G. A.; Shutenkova, T. V.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1988 , vol. 37, p. 1612 - 1616 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1988 , # 8 p. 1806 - 1811 Title/Abstract Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

314

Synthesize Find similar Rx-ID: 6218224

Find similar reactions

With (C6H5)3Bilt;OOC(CH3)3gt;2

Yield given. Yields of byproduct given;

Dodonov, V. A.; Zinov'eva, T. I.; Osadchaya, N. N.

J. Gen. Chem. USSR (Engl. Transl.), 1988 , vol. 58, # 3 p. 712,630 - 631 Title/Abstract Full Text Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

315

Synthesize Find similar Rx-ID: 26487292

Synthesize Find similar


Find similar reactions

Leising, Randolph A.; Takeuchi, Kenneth J.

Journal of the American Chemical Society, 1988 , vol. 110, # 12 p. 4079 - 4080 Title/Abstract Full Text View citing articles Show Details

in water

Kinetics; pH = 6.8; kinetics measured by UV-Vis spectrophotometry, product distribution determined by GC;

A

B

Synthesize Find similar

Synthesize Find similar

316

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26487294

Find similar reactions

A: >99

Marmion, Mary E.; Takeuchi, Kenneth J.

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1988 , p. 2385 - 2392 Title/Abstract Full Text Show Details

in water

Kinetics; 25°C, 3 h, pH 2, reaction monitored by UV-spectroscopy;; separation by addn of pentane, complex identified by UV-spectroscopy, organic product by g.c.-m.s.;

A

B

Synthesize Find similar

Synthesize Find similar

317

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26487295

Find similar reactions

A: >99

Marmion, Mary E.; Takeuchi, Kenneth J.

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1988 , p. 2385 - 2392 Title/Abstract Full Text Show Details

in dichloromethane; acetonitrile

Kinetics; 25°C, 3 h, reaction monitored by UV-spectroscopy;; separation by addn of pentane, complex identified by UV-spectroscopy, organic product by g.c.-m.s.;

A

B

Synthesize

Synthesize

318

Synthesize Find similar

Synthesize Find similar


Find similar

Rx-ID: 26487296

Find similar reactions

A: >99

Find similar

Marmion, Mary E.; Takeuchi, Kenneth J.

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1988 , p. 2385 - 2392 Title/Abstract Full Text Show Details

in water

Kinetics; 25°C, pH 2.0, 3 h, reaction monitored by UV-spectroscopy;; extn. of organic product with pentane, complex identified by UV-spectroscopy, organic product by g.c.-m.s.;

A

B

Synthesize Find similar

Synthesize Find similar

319

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26487297

Find similar reactions

A: >99

Marmion, Mary E.; Takeuchi, Kenneth J.

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1988 , p. 2385 - 2392 Title/Abstract Full Text Show Details

in dichloromethane; acetonitrile

Kinetics; 25°C, 2.0, 3 h, reaction monitored by UV-spectroscopy;; separation by addn. of pentane, complex identified by UV-spectroscopy, organic product by g.c.-m.s.;

A

B

Synthesize Find similar

Synthesize Find similar

320

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26487300

Find similar reactions

A: >99

A

321

Marmion, Mary E.; Takeuchi, Kenneth J.

Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1988 , p. 2385 - 2392 Title/Abstract Full Text Show Details

in dichloromethane; acetonitrile

Kinetics; 25°C, 3 h, reaction monitored by UV-spectroscopy;; separation by addn. of pentane, complex identified by UV-spectroscopy, organic product by g.c.-m.s.;

B


Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838448

Find similar reactions

A: 20 % Chromat. B: 60 % Chromat.

Synthesize Find similar

Synthesize Find similar

With dihydridotetrakis(triphenylphosphine)ruthenium in toluene

10 h; Heating;

Minami, Ichiro; Tsuji, Jiro

Tetrahedron, 1987 , vol. 43, # 17 p. 3903 - 3916 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

322

Synthesize Find similar Rx-ID: 3840143

Find similar reactions

A: 20 % Chromat. B: 60 % Chromat.

With allyl methyl carbonate; dihydridotetrakis(triphenylphosphine)ruthenium in toluene

10 h; Heating;

Minami, Ichiro; Tsuji, Jiro

Tetrahedron, 1987 , vol. 43, # 17 p. 3903 - 3916 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

323

Synthesize Find similar

Synthesize Find similar

Rx-ID: 26152903

Find similar reactions

A: 85% B: 40%

in acetonitrile

Irradiation (UV/VIS); under argon; FcPF6 and benzylalcohol are dissolved in MeCN and irradiated (>300 nm) for 1 h; detn. of ferrocene by UV-Vis spectroscopy;

Divisia-Blohorn, B.; Paltrier, M.

Inorganica Chimica Acta, 1987 , vol. 131, p. 65 - 68 Full Text View citing articles Show Details

A: 75%

in acetonitrile

Irradiation (UV/VIS); under argon; FcPF6 and benzylalcohol are dissolved in MeCN and irradiated (>300 nm) for 21 h; detn. of ferrocene by UV-Vis spectroscopy;

Divisia-Blohorn, B.; Paltrier, M.

Inorganica Chimica Acta, 1987 , vol. 131, p. 65 - 68 Full Text View citing articles Show Details

A

B


324

Synthesize Find similar Rx-ID: 3840151

Find similar reactions

Synthesize Find similar

Synthesize Find similar

A: 14% B: 70%

With periodic acid in 1,4-dioxane; water

T=100°C; other substrates; Mechanism;

Bhatt, M. V.; Hosur, B. M.

Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1986 , vol. 25, p. 1004 - 1005 Title/Abstract Full Text Show Details

A: 14% B: 70%

With periodic acid in 1,4-dioxane; water

T=100°C;

Bhatt, M. V.; Hosur, B. M.

Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1986 , vol. 25, p. 1004 - 1005 Title/Abstract Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

325

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838950

Find similar reactions

A: 7 % Spectr. B: 72 % Spectr.

With diethyl ether; iodosylbenzene; boron trifluoride in 1,4-dioxane

0.5 h; Ambient temperature;

Ochiai, Masahito; Fujita, Eiichi; Arimoto, Masao; Yamaguchi, Hideo

Chemical and Pharmaceutical Bulletin, 1985 , vol. 33, # 1 p. 41 - 47 Title/Abstract Full Text Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

326

Synthesize Find similar Rx-ID: 3839218

Find similar reactions

Synthesize Find similar


Dodonov, V. A.; Gushchin, A. V.; Brilkina, T. G.

J. Gen. Chem. USSR (Engl. Transl.), 1985 , vol. 55, # 1 p. 73 - 80,63 - 68 Title/Abstract Full Text Show Details

in toluene

T=80°C; 22 h; Yield given. Yields of byproduct given;

A

B

Synthesize Find similar

Synthesize Find similar

327

Synthesize Find similar Rx-ID: 3840144

Find similar reactions

B: 57.4%

With air; antimonypentachloride; dimethyl sulfoxide in nitromethane

T=60°C; 3 h; Product distribution;

Yamamoto, Jiro; Ito, Satoshi; Tsuboi, Takashi; Tsuboi, Toshiaki; Tsukihara, Kumiko

Bulletin of the Chemical Society of Japan, 1985 , vol. 58, # 2 p. 470 - 472 Title/Abstract Full Text Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

328

Synthesize Find similar Rx-ID: 3840160

Find similar reactions

With triphenylbismuth(V) diacetate in toluene

T=80°C; 22 h; Yield given. Yields of byproduct given;

Dodonov, V. A.; Gushchin, A. V.; Brilkina, T. G.

J. Gen. Chem. USSR (Engl. Transl.), 1985 , vol. 55, # 1 p. 73 - 80,63 - 68 Title/Abstract Full Text Show Details

329

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2818063

Find similar reactions


With silver carbonate

Smith, John R. Lindsay; Nee, Michael W.; Noar, J. Barry; Bruice, Thomas C.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984 , # 2 p. 255 - 260 Title/Abstract Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

330

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3537475

Find similar reactions

With dipotassium peroxodisulfate in water

T=80°C; 0.5 h; var. ratio of reac. partners; Product distributionMechanism;

Eberhardt, Manfred K.

Tetrahedron Letters, 1984 , vol. 25, # 34 p. 3663 - 3666 Title/Abstract Full Text View citing articles Show Details

331

Synthesize Find similar

Rx-ID: 3838185

Find similar reactions

98%

Synthesize Find similar

Synthesize Find similar

Kanemoto, Sigekazu; Saimoto, Hiroyuki; Oshima, Koichiro; Nozaki, Hitosi

Tetrahedron Letters, 1984 , vol. 25, # 31 p. 3317 - 3320 Title/Abstract Full Text View citing articles Show Details

With Cr(OAc)3 impregnated NafionR 511 in chlorobenzene; benzene

T=85°C; 6 h;

332

Synthesize Find similar

Multi-step reaction with 2 steps 1: Fe(II), H2O / acetonitrile

Synthesize Find similar

Rx-ID: 19144777

Find similar reactions

Sugimoto, Hiroshi; Sawyer, Donald T.

Journal of the American Chemical Society, 1984 , vol. 106, # 15 p. 4283 - 4285


Title/Abstract Full Text View citing articles Show Details

2: Fe(II), H2O2 / acetonitrile View Scheme

A

B

Synthesize Find similar

Synthesize Find similar

333

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838211

Find similar reactions

With chromium(VI) oxide

Multistep reaction, var. alcohols, oximes and disulfides; Product distribution;

Aizpurua, J. M.; Palomo, Claudio

Tetrahedron Letters, 1983 , vol. 24, # 40 p. 4367 - 4370 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

334

Synthesize Find similar Rx-ID: 3838363

Find similar reactions

A: 28 % Turnov. B: 18 % Turnov. C: 46 % Turnov. D: 11 % Turnov.

Synthesize Find similar

Haszeldine, Robert N.; Raynor, Clive M.; Tipping, Anthony E.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 11 p. 2801 - 2806 Title/Abstract Full Text Show Details

T=240°C; 72 h;

A

335

B

C

D


Synthesize Find similar

Synthesize Find similar

Rx-ID: 3840109

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Tomioka, Hideo; Nakamura, Hiroyuki; Izawa, Yasuji

Journal of the Chemical Society, Chemical Communications, 1983 , # 19 p. 1070 - 1071 Title/Abstract Full Text View citing articles Show Details

T=10°C; 0.333333 h; Irradiation; Yield given. Yields of byproduct given;

A

B

Synthesize Find similar

Synthesize Find similar

336

Synthesize Find similar Rx-ID: 6221071

Find similar reactions

A: 6% B: 6 % Turnov.

Haszeldine, Robert N.; Raynor, Clive M.; Tipping, Anthony E.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 11 p. 2801 - 2806 Title/Abstract Full Text Show Details

T=240°C; 72 h;

A

B

Synthesize Find similar

Synthesize Find similar

337

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3480667

Find similar reactions

With cesium hydroxide; 2,4-dimethyl-6-tert-butylphenol in water; N,N-dimethyl-formamide

Rate constant;

Shinkai, Seiji; Kuroda, Hideo; Manabe, Osamu

Tetrahedron Letters, 1982 , vol. 23, # 13 p. 1357 - 1360 Title/Abstract Full Text View citing articles Show Details

A

338

B

C

D

E

F


Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838546

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

With lt;Ru(CO)3gt;2; hydrogen iodide; hydrogen

T=220°C; 3 h; var. benzyl compounds; or benzaldehyd; other reagents, temp.,times; Product distributionMechanism;

Synthesize Find similar

Synthesize Find similar

Hardin, Simon G.; Turney, Terence W.

Australian Journal of Chemistry, 1982 , vol. 35, # 8 p. 1599 - 1608 Title/Abstract Full Text Show Details

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

339

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838593

Find similar reactions

in dichloromethane

T=60 - 70°C; 18 h; Yield given. Yields of byproduct given;

Balsells, R. Erra; Frasca, A. R.

Tetrahedron, 1982 , vol. 38, # 16 p. 2525 - 2538 Title/Abstract Full Text View citing articles Show Details

in dichloromethane

T=60 - 70°C; 18 h; thermal stability;

Balsells, R. Erra; Frasca, A. R.

Tetrahedron, 1982 , vol. 38, # 16 p. 2525 - 2538 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

340

Synthesize Find similar Rx-ID: 3838857

Find similar reactions

Synthesize Find similar

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar


341

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838860

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

342

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838862

Find similar reactions

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

343

Synthesize Find similar Rx-ID: 3839074

Find similar reactions

T=90°C; 10 h; Product distribution;

Synthesize Find similar

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details


A

B

Synthesize Find similar

Synthesize Find similar

344

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839075

Find similar reactions

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

345

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839080

Find similar reactions

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

346

Synthesize Find similar Rx-ID: 3839085

Find similar reactions

T=90°C; 10 h; Product distribution;

Synthesize Find similar

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details


A

B

Synthesize Find similar

Synthesize Find similar

347

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839094

Find similar reactions

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

348

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839095

Find similar reactions

Yoneda, Fumio; Hirayama, Ryiochi; Yamashita, Machiko

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 301 - 304 Title/Abstract Full Text Show Details

T=90°C; 10 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

349

Synthesize Find similar Rx-ID: 3840146

Find similar reactions

With ethenetetracarbonitrile in ethyl acetate

Heating; Product distribution;

Nasakin, O. E.; Petrov, G. N.; Alekseev, V. V.; Promonenkov, V. K.; Sukhobokov, A. v.

J. Appl. Chem. USSR (Engl. Transl.), 1982 , vol. 55, # 6 p. 1399 - 1402,1286 - 1289 Title/Abstract Full Text Show Details


A

B

C

D

E

F

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

350

Synthesize Find similar Rx-ID: 3840149

Find similar reactions

Balsells, R. Erra; Frasca, A. R.

Tetrahedron, 1982 , vol. 38, # 16 p. 2525 - 2538 Title/Abstract Full Text View citing articles Show Details

in dichloromethane

T=60 - 70°C; 18 h; Irradiationwithout solvent, other reaction time and further light sources; Product distributionMechanism;

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

351

Synthesize Find similar Rx-ID: 3840150

Find similar reactions

Balsells, R. Erra; Frasca, A. R.

Tetrahedron, 1982 , vol. 38, # 16 p. 2525 - 2538 Title/Abstract Full Text View citing articles Show Details

in dichloromethane

T=60 - 70°C; 18 h; Irradiation; Yield given. Further byproducts given. Yields of byproduct given;

A

B

Synthesize Find similar

Synthesize Find similar

352

Synthesize Find similar Rx-ID: 3840153

Find similar reactions

A: 82%

With N,N-dichloro-t-butylamine in tetrachloromethane

Ogata, Yoshiro; Kimura, Makoto


B: 20 % Chromat.

T=20°C; 1 h; Irradiation; Product distribution;

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 947 - 950 Title/Abstract Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

353

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2987189

Find similar reactions

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

354

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2988987

Find similar reactions

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

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

355

Synthesize Find similar Rx-ID: 3744744

Find similar reactions

Synthesize Find similar


Moreno-Manas, M.; Trius, A.

Tetrahedron, 1981 , vol. 37, # 17 p. 3009 - 3016 Title/Abstract Full Text View citing articles Show Details

T=140°C;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

356

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3744745

Find similar reactions

A: 8% B: 10% C: 32%

With palladium(II) acetylacetonate; triphenylphosphine

T=140°C; 48 h;

Moreno-Manas, M.; Trius, A.

Tetrahedron, 1981 , vol. 37, # 17 p. 3009 - 3016 Title/Abstract Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

357

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838563

Find similar reactions

A: 59% B: 64% C: 35%

Banks, Ronald E.; Birchall, J. Michael; Haszeldine, Robert N.; Hughes, Raymond A.; Nona, Shmaiel N.; Stephens, Christopher W.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 455 - 456 Title/Abstract Full Text View citing articles Show Details

T=20°C; 0.0333333 h; analogous reactions of other benzyl derivatives (PhCH2CN, PhCH2Cl, and PhCH2N3); various reactant ratio; MechanismProduct distribution;

A

B

Synthesize Find similar

Synthesize Find similar

358

Synthesize Find similar Rx-ID: 3839131

Synthesize Find similar


Find similar reactions

With potassium tert-butylate

T=80°C; 8 h; other alcohol; Product distributionMechanism;

Shinkai, Seiji; Hamada, Hisatake; Kuroda, Hideo; Manabe, Osamu

Journal of Organic Chemistry, 1981 , vol. 46, # 11 p. 2333 - 2338 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

359

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3840113

Find similar reactions

A: 90%

With potassium tert-butylate

T=80°C; 2 h; in the dark; Product distribution;

Yoneda, Fumio; Tsukuda, Kinshiro; Kawazoe, Michiko; Sone, Atsuko; Koshiro, Akira

Journal of Heterocyclic Chemistry, 1981 , vol. 18, p. 1329 - 1334 Title/Abstract Full Text Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

360

Synthesize Find similar Rx-ID: 3840147

Find similar reactions

A: 59% B: 64% C: 35%

With bis-trifluoromethyl-aminooxyl

T=20°C; 0.0333333 h;

Banks, Ronald E.; Birchall, J. Michael; Haszeldine, Robert N.; Hughes, Raymond A.; Nona, Shmaiel N.; Stephens, Christopher W.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 455 - 456 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize

Synthesize

361

Synthesize Find similar

Synthesize Find similar


Find similar

Rx-ID: 4293139

Find similar reactions

Find similar

With tris(triphenylphosphine)ruthenium(II) chloride in various solvent(s) T=170 - 190°C; var. reactants and reaction partner; KineticsMechanism;

Speier, Gabor; Marko, Laszlo

Journal of Organometallic Chemistry, 1981 , vol. 210, # 2 p. 253 - 262 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

362

Synthesize Find similar Rx-ID: 7453117

Find similar reactions

With d,oxyde de cuivre

T=176°C; 6 h; Heatingin liquid phase;

Berthon, Bruno; Forestiere, Alain; Leleu, Gerard; Sillion, Bernard

Tetrahedron Letters, 1981 , vol. 22, # 41 p. 4073 - 4076 Title/Abstract Full Text View citing articles Show Details

With copper(II) oxide

T=176°C; 6 h;

Berthon, Bruno; Forestiere, Alain; Leleu, Gerard; Sillion, Bernard

Tetrahedron Letters, 1981 , vol. 22, # 41 p. 4073 - 4076 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

363

Synthesize Find similar Rx-ID: 1797297

Find similar reactions

Synthesize Find similar

Packer, John E.; Heigway, Christopher J.; Miller, Helen M.; Dobson, Brian C.

Australian Journal of Chemistry, 1980 , vol. 33, # 5 p. 965 - 977 Title/Abstract Full Text Show Details

in water

Rate constant;

A

B


364

Synthesize Find similar

Synthesize Find similar

Rx-ID: 1834986

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Packer, John E.; Heigway, Christopher J.; Miller, Helen M.; Dobson, Brian C.

Australian Journal of Chemistry, 1980 , vol. 33, # 5 p. 965 - 977 Title/Abstract Full Text Show Details

in water

Rate constant;

A

B

Synthesize Find similar

Synthesize Find similar

365

Synthesize Find similar

Synthesize Find similar

Rx-ID: 1842106

Find similar reactions

Packer, John E.; Heigway, Christopher J.; Miller, Helen M.; Dobson, Brian C.

Australian Journal of Chemistry, 1980 , vol. 33, # 5 p. 965 - 977 Title/Abstract Full Text Show Details

in water

Rate constant;

A

B

Synthesize Find similar

Synthesize Find similar

366

Synthesize Find similar Rx-ID: 1975149

Find similar reactions

in water

Rate constant;

Synthesize Find similar

Packer, John E.; Heigway, Christopher J.; Miller, Helen M.; Dobson, Brian C.

Australian Journal of Chemistry, 1980 , vol. 33, # 5 p. 965 - 977 Title/Abstract Full Text Show Details


A

B

Synthesize Find similar

Synthesize Find similar

367

Synthesize Find similar

Synthesize Find similar

Rx-ID: 1975314

Find similar reactions

Packer, John E.; Heigway, Christopher J.; Miller, Helen M.; Dobson, Brian C.

Australian Journal of Chemistry, 1980 , vol. 33, # 5 p. 965 - 977 Title/Abstract Full Text Show Details

in water

Rate constant;

A

B

Synthesize Find similar

Synthesize Find similar

368

Synthesize Find similar

Synthesize Find similar

Rx-ID: 2343179

Find similar reactions

B: 76 % Chromat.

With tin(IV) ethoxide in toluene

T=110°C; 20 h;

Casiraghi, Giovanni; Casnati, Giuseppe; Sartori, Giovanni; Zanafredi, Girolamo T.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1980 , p. 407 - 411 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

369

Synthesize Find similar Rx-ID: 3127441

Find similar reactions

A: 296 %

With potassium carbonate

T=90°C; 5 h; Product distribution;

Synthesize Find similar

Yoneda, Fumio; Tsukuda, Kinshiro; Shinozuka, Kazuo; Hirayama, Fumitoshi; Uekama, Kaneto; Koshiro, Akira

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3049 - 3056 Title/Abstract Full Text Show Details


A

B

Synthesize Find similar

Synthesize Find similar

370

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3135468

Find similar reactions

B: 128 % Chromat.

With potassium carbonate

T=90°C; 10 h; oxidation of benzyl alcohol and benzylamine by various 5-deazaflavins as oxido-reductive catalyst;

Yoneda; Mori; Ono; et al.

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 12 p. 3514 - 3520 Title/Abstract Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

371

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3150970

Find similar reactions

A: 199 %

Yoneda, Fumio; Tsukuda, Kinshiro; Shinozuka, Kazuo; Hirayama, Fumitoshi; Uekama, Kaneto; Koshiro, Akira

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3049 - 3056 Title/Abstract Full Text Show Details

T=90°C; 5 h; Rate constant;

A

B

Synthesize Find similar

Synthesize Find similar

372

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3838609

Find similar reactions

With lithium perchlorate in acetonitrile

competitive anodic oxidation; isotope effect; Product distribution;

Boyd, Jean W.; Schmalzl, Paul W.; Miller, Larry L.

Journal of the American Chemical Society, 1980 , vol. 102, # 11 p. 3856 - 3862 Title/Abstract Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

373

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839421

Find similar reactions

A: 51%

With air; potassium carbonate

T=90°C; 10 h; further alcohol or amine, further 2H-pyrido<1',2':1,6>pyrido<2,3-d>pyrimidine-2,4(3H)dione ("bent 5-deazaflavin"); Product distribution;

Yoneda, Fumio; Ono, Masami; Kira, Keiko; Tanaka, Hisako; Sakuma, Yoshiharu

Chemistry Letters, 1980 , p. 817 - 820 Title/Abstract Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

374

Synthesize Find similar

Synthesize Find similar

Rx-ID: 3839502

Find similar reactions

A: 399 %

Yoneda, Fumio; Tsukuda, Kinshiro; Shinozuka, Kazuo; Hirayama, Fumitoshi; Uekama, Kaneto; Koshiro, Akira

Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3049 - 3056 Title/Abstract Full Text Show Details

T=90°C; 5 h; Product distribution;

A

B

Synthesize Find similar

Synthesize Find similar

375

Synthesize Find similar Rx-ID: 3839633

Find similar reactions

A: 214 %

T=90°C; 5 h; Product distribution;

Synthesize Find similar

Yoneda, Fumio; Tsukuda, Kinshiro; Shinozuka, Kazuo; Hirayama, Fumitoshi; Uekama, Kaneto; Koshiro, Akira


Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3049 - 3056 Title/Abstract Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

376

Synthesize Find similar Rx-ID: 5819711

Find similar reactions

Mastagli; de Fournas

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1959 , vol. 248, p. 1352 Full Text View citing articles Show Details

T=140°C;

A

B

C

D

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

377

Synthesize Find similar

Synthesize Find similar

Rx-ID: 642903

Find similar reactions

Jakowlew; Popa

Zhurnal Obshchei Khimii, 1958 , vol. 28, p. 2475; engl. Ausg. S. 2510 Full Text View citing articles Show Details

T=450°C; Leiten ueber einen Chrom-Mangan-Katalysator;

378

Synthesize Find similar

T=229 - 236°C; Rate constant;

Synthesize Find similar

Rx-ID: 5819624

Find similar reactions

Balandin; Teteni

Doklady Akademii Nauk SSSR, 1957 , vol. 113, p. 1090


Doklady Physical Chemistry, 112-117<1957>235 Full Text View citing articles Show Details

379

Synthesize Find similar

Rx-ID: 146477

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Orazi; Corral

Anales de la Asociacion Quimica Argentina (1921-2001), 1954 , vol. 42, p. 139,145 Full Text Show Details

T=25°C; Rate constant;

380

Synthesize Find similar

Rx-ID: 154499

Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Orazi; Corral

Anales de la Asociacion Quimica Argentina (1921-2001), 1954 , vol. 42, p. 139,145 Full Text Show Details

T=25°C; Kinetics;

381

Synthesize Find similar

Rx-ID: 5819630

Find similar reactions

T=25°C; UV-Licht (λ: 365 nm).Irradiation; Kinetics;

Synthesize Find similar

Synthesize Find similar

Bates; Uri

Journal of the American Chemical Society, 1953 , vol. 75, p. 2754,2756


Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

382

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5673499

Find similar reactions

BARAKAT; MOUSA

The Journal of pharmacy and pharmacology, 1952 , vol. 4, # 2 p. 115 - 117 Title/Abstract Full Text Show Details

T=90°C;

A

B

Synthesize Find similar

Synthesize Find similar

383

Synthesize Find similar Rx-ID: 5819709

Find similar reactions

Mastagli et al.

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1951 , vol. 232, p. 1848 Full Text Show Details

T=150°C;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

384

Synthesize Find similar Rx-ID: 5957242

Find similar reactions


Mastagli et al.

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1951 , vol. 232, p. 1848 Full Text Show Details

T=275 - 290°C;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

385

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5958068

Find similar reactions

Farkas; Schaechter

Journal of the American Chemical Society, 1949 , vol. 71, p. 2828 Chem.Abstr., 1948 , p. 7313 Full Text View citing articles Show Details

T=50 - 80°C;

386

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5819616

Find similar reactions

Metayer; Roumens

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1947 , vol. 225, p. 1324 Full Text View citing articles Show Details

387

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5819617

Find similar reactions

Palfray; Metayer; Panouse

Bulletin de la Societe Chimique de France, 1947 , p. 766,770 Full Text View citing articles Show Details


Panouse

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1946 , vol. 223, p. 745 Full Text View citing articles Show Details

388

Synthesize Find similar

Synthesize Find similar

Rx-ID: 6214137

Find similar reactions

Cubberley; Mueller

Journal of the American Chemical Society, 1946 , vol. 68, p. 1150 Full Text View citing articles Show Details

T=200 - 300°C; Equilibrium constant;

A

B

Synthesize Find similar

Synthesize Find similar

389

Synthesize Find similar Rx-ID: 5958026

Find similar reactions

Davies; Hodgson

Journal of the Chemical Society, 1943 , p. 281 Full Text View citing articles Show Details

T=300 - 350°C; Leiten ueber einen Kupfer-Silber-Bimsstein-Katalysator;

390

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5819688

Find similar reactions

Fisher; Eisner

Journal of Organic Chemistry, 1941 , vol. 6, p. 169,172 Full Text View citing articles Show Details


A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

391

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5958737

Find similar reactions

Meerwein

Journal fuer Praktische Chemie (Leipzig), 1936 , vol. <2> 147, p. 211,225 Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

392

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5958738

Find similar reactions

Meerwein

Journal fuer Praktische Chemie (Leipzig), 1936 , vol. <2> 147, p. 211,225 Full Text View citing articles Show Details

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

393

Synthesize Find similar Rx-ID: 5958739

Find similar reactions

Synthesize Find similar

Meerwein

Journal fuer Praktische Chemie (Leipzig), 1936 , vol. <2> 147, p. 211,225 Full Text View citing articles Show Details


A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

394

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5958740

Find similar reactions

Meerwein

Journal fuer Praktische Chemie (Leipzig), 1936 , vol. <2> 147, p. 211,225 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

395

Synthesize Find similar

Synthesize Find similar

Rx-ID: 6211162

Find similar reactions

Rubinschtein; Lukaschina

Uc. Zap. Moskovsk. Univ., 1936 , # 6 p. 299,303 Chem. Zentralbl., 1938 , vol. 109, # I p. 3608 Full Text Show Details

T=400°C; Leiten ueber MoO3/Bimsstein;

A

B

Synthesize Find similar

Synthesize Find similar

396

Synthesize Find similar Rx-ID: 5958045

Find similar reactions


T=70°C;

McKee; Heard

Trans. electroch. Soc., 1934 , vol. 65, p. 301,316 Full Text Show Details


Turn static files into dynamic content formats.

Create a flipbook
Issuu converts static files into: digital portfolios, online yearbooks, online catalogs, digital photo albums and more. Sign up and create your flipbook.