2-Naphthaldehyde (β-Naphthaldehyde) by Asch

Reaxys

PubChem

eMolecules

Reactions (187)

Yield

Substances (1)

Citations (319)

Conditions

References

100

Synthesize Find similar Multi-step reaction with 3 steps 1: 1.69 g / SnBr2 / CH2Cl2 / 20 °C 2: 88 percent / Rhodococcus rhodochrous IFO 15564; phosphate buffer / H2O; ethanol; hexane / 24 h / 30 °C / pH 6.0 3: 35 percent / nitrosylsulfuric acid / dimethylformamide / 24 h / 20 °C View Scheme

101

Synthesize Find similar

Rx-ID: 14693035 Find similar reactions

Kimura, Mayumi; Kuboki, Atsuhito; Sugai, Takeshi

Tetrahedron Asymmetry, 2002 , vol. 13, # 10 p. 1059 - 1068 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar Multi-step reaction with 2 steps 1: 75 percent / Rhodococcus rhodochrous IFO 15564; phosphate buffer / H2O; dimethylformamide; hexane / 24 h / 30 °C / pH 6.0 2: 6 percent / nitrosylsulfuric acid / dimethylformamide / 0.5 h / 0 °C View Scheme

Synthesize Find similar

Rx-ID: 14698006 Find similar reactions

Kimura, Mayumi; Kuboki, Atsuhito; Sugai, Takeshi

Tetrahedron Asymmetry, 2002 , vol. 13, # 10 p. 1059 - 1068 Title/Abstract Full Text View citing articles Show Details

102

Synthesize Find similar Multi-step reaction with 2 steps 1: 88 percent / Rhodococcus rhodochrous IFO 15564; phosphate buffer / H2O; ethanol; hexane / 24 h / 30 °C / pH 6.0 2: 35 percent / nitrosylsulfuric acid / dimethylformamide / 24 h / 20 °C View Scheme

Synthesize Find similar

Rx-ID: 14709375 Find similar reactions

Kimura, Mayumi; Kuboki, Atsuhito; Sugai, Takeshi

Tetrahedron Asymmetry, 2002 , vol. 13, # 10 p. 1059 - 1068 Title/Abstract Full Text View citing articles Show Details

103

Synthesize Find similar Multi-step reaction with 3 steps 1: 45 percent / immobilized Burkholderia cepacia lipase; phosphate buffer; NaOH / decane; H2O / 38 h / 30 °C / pH 7.0 2: 75 percent / Rhodococcus rhodochrous IFO 15564;

Synthesize Find similar

Rx-ID: 14710126 Find similar reactions

Kimura, Mayumi; Kuboki, Atsuhito; Sugai, Takeshi

Tetrahedron Asymmetry, 2002 , vol. 13, # 10 p. 1059 - 1068 Title/Abstract Full Text View citing articles Show Details

phosphate buffer / H2O; dimethylformamide; hexane / 24 h / 30 °C / pH 6.0 3: 6 percent / nitrosylsulfuric acid / dimethylformamide / 0.5 h / 0 °C View Scheme

104

Synthesize Find similar

Hide Experimental Procedure

Synthesize Find similar

Rx-ID: 24142464 Find similar reactions

Cai, Sui Xiong; Drewe, John A.; Zhang, Han-Zhong

Patent: US2002/128292 A1, 2002 ; Title/Abstract Full Text Show Details

24:5-Chloro-indole-2-carboxylic Acid (2-Naphthylidene)-hydrazide

From 5-chloro-indole-2-carboxylic acid hydrazide (63 mg, 0.3 mmol), 2-naphthaldehyde (46 mg, 0.3 mmol) was obtained 65 mg (62percent) of the title compound. 1H NMR (DMSO-d6): 12.00 (bs, 1H), 8.60 (s, 1H), 8.18 (s, 1H), 8.10-7.20 (m, 12H). A

Synthesize Find similar

105

Synthesize Find similar Rx-ID: 8988232 Find similar reactions

A: 10 % Chromat. B: 60 % Spectr.

106

With hydrogen; trimethylacetic anhydride; tetrakis(triphenylphosphine) palladium(0) in tetrahydrofuran

T=80°C; P=45003.6 Torr; 24 h;

Nagayama; Shimizu; Yamamoto

Bulletin of the Chemical Society of Japan, 2001 , vol. 74, # 10 p. 1803 - 1815 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar Herstellung von <α-14C><2>Naphthaldehyd;

Rx-ID: 5855801 Find similar reactions

Catch; Evans

Journal of the Chemical Society, 1957 , p. 2796,2799 Full Text View citing articles Show Details

Olah,G.A.; Kuhn,S.J.

Journal of the American Chemical Society, 1960 , vol. 82, p. 2380 - 2382 Full Text View citing articles Show Details

Lightner,D.A. et al.

Journal of the American Chemical Society, 1972 , vol. 94, # 10 p. 3492 - 3497 Full Text View citing articles Show Details

Yasuhara,A. et al.

Bulletin of the Chemical Society of Japan, 1972 , vol. 45, p. 3638 - 3645 Full Text View citing articles Show Details

Rigaudy,J.; Maumy,M.

Bulletin de la Societe Chimique de France, 1972 , p. 3936 - 3941 Full Text View citing articles Show Details

Mamalis,P. et al.

Journal of the Chemical Society, 1960 , p. 229 - 238 Full Text View citing articles Show Details

Ando,W.; Sekiguchi,A.

Journal of Organometallic Chemistry, 1977 , vol. 133, p. 219 - 230 Full Text View citing articles Show Details

Paquette; Birnberg

Journal of Organic Chemistry, 1975 , vol. 40, p. 1709,1711 Full Text Show Details

Backeberg; Staskun

Journal of the Chemical Society, 1962 , p. 3961 Full Text Show Details

Muxfeldt et al.

Chemische Berichte, 1965 , vol. 98, p. 3040 Full Text Show Details

Sisti et al.

Journal of Chemical and Engineering Data, 1964 , vol. 9, p. 108 Full Text View citing articles Show Details

Chatterjea; Prasad

Journal of the Indian Chemical Society, 1960 , vol. 37, p. 357,359 Full Text Show Details

Degani; Fochi

Synthesis, 1976 , p. 757 Full Text Show Details

Ertel; Friedrich

Chemische Berichte, 1977 , vol. 110, p. 86,95 Full Text Show Details

van Es; Staskun

Journal of the Chemical Society, 1965 , p. 5775 Full Text Show Details

Staskun; Backeberg

Journal of the Chemical Society, 1964 , p. 5880 Full Text Show Details

Brown; Tsukamoto

Journal of the American Chemical Society, 1964 , vol. 86, p. 1089,1092 Full Text Show Details

Syper

Tetrahedron Letters, 1967 , p. 4193 Full Text View citing articles Show Details

Horner; Roeder

Chemische Berichte, 1970 , vol. 103, p. 2984 Full Text Show Details

Lee; Spitzer

Journal of Organic Chemistry, 1970 , vol. 35, p. 3589 Full Text View citing articles Show Details

Kaberia; Vickery

Journal of the Chemical Society, Chemical Communications, 1978 , p. 459 Full Text View citing articles Show Details

Costa et al.

Journal of Heterocyclic Chemistry, 1974 , vol. 11, p. 943,947,948 Full Text Show Details

Sekine; Kamiya

Kogyo Kagaku Zasshi, 1967 , vol. 70, p. 59,60,61 Full Text Show Details

Sarbhai; Mathur

Indian Journal of Applied Chemistry, 1969 , vol. 32, p. 393 Full Text Show Details

Rus'janowa; Muljaewa

Neftekhimiya, 1971 , vol. 11, p. 537 Chem.Abstr., 1971 , vol. 75, # 129151 Full Text Show Details

Sitkin et al.

Zhurnal Organicheskoi Khimii, 1975 , vol. 11, p. 452,443 Full Text Show Details

Georgiew; Sheljaskow

Doklady Chemistry, 1964 , vol. 154, p. 4 Doklady Akademii Nauk SSSR, 1964 , vol. 154, p. 132 Full Text Show Details

Kremlev et al.

Zhurnal Organicheskoi Khimii, 1970 , vol. 6, p. 793,795 Full Text Show Details

Hide Experimental Procedure

Basu; Amaresh; Gahman; Timothy C.; Girten; Beverly E.; Griffith; Michael C.; Hecht; Curtis C.; Kiely; John S.; Slivka; Sandra R.

Patent: US6127381 A1, 2000 ; Title/Abstract Full Text Show Details

The remaining teabags of amino acid on resin were each reacted as above in separate reactions with the following 94 aldehydes such that all combinations of 4-carboxy disubstituted dihydroisoquinolones were formed as indicated in the following (R2) list: ... 2,6-difluorobenzaldehyde, 2-bromobenzaldehyde, 2-chloro-5-nitrobenzaldehyde, 2-chloro-6-fluorobenzaldehyde, 2-cyanobenzaldehyde, 2-fluorobenzaldehyde, 2-furaldehyde, 2-imidazolecarboxaldehyde, 2-methoxybenzaldehyde (o-anisaldehyde), 2-naphthaldehyde, 2-pyridinecarboxaldehyde, 2-quinolinecarboxaldehyde, 2-thiophenecarboxaldehyde, 3,4-(methylenedioxy)benzaldehyde (piperonal), ...

Hide Experimental Procedure

Petrolite Corporation

Patent: US4311841 A1, 1982 ; Title/Abstract Full Text Show Details

Typical examples of aldehyde and polyamines employed in preparing these Schiff bases include the following: ALDEHYDES Benzaldehyde ... 4-methylbenzaldehyde 2-methoxybenzaldehyde 4-methoxybenzaldehyde 2-naphthaldehyde 1-naphthaldehyde 4-phenylbenzaldehyde Propionaldehyde ...

Hide Experimental Procedure

Schering Corporation

Patent: US4376769 A1, 1983 ; Title/Abstract Full Text Show Details

These aldehydes and ketones are set forth for exemplification and are not to be construed as limiting the scope of this invention. benzaldehyde, ... 2-methylbenzaldehyde, 4-methylbenzaldehyde, 3-trifluoromethylbenzaldehyde, 1,1-biphenyl-4-carboxaldehyde, 2-naphthylaldehyde, 6-methoxy-2-naphthaldehyde, 1,1-biphenylacetaldehyde, 2-methyl-3-chlorobenzaldehyde, ...

Hide Experimental Procedure

Ethyl Corporation

Patent: US4837327 A1, 1989 ; Title/Abstract Full Text Show Details

A few illustrative examples of preferred aldehydes include ...

4-methoxy-1-naphthaldehyde 3-methyl-p-anisaldehyde 10-methylanthracene-9-carboxaldehyde 1-naphthaldehyde 2-naphthaldehyde pentafluorobenzaldehyde phenanthrene-9-carboxaldehyde o-phthalicdicarboxaldehyde ...

Hide Experimental Procedure

Smith Kline and French Laboratories Limited

Patent: US4185103 A1, 1980 ; Title/Abstract Full Text Show Details

Substitution of the following aldehydes: (a) Naphthalene-1-carboxaldehyde (b) Naphthalene-2-carboxaldehyde (c) 2,3-Dihydro-1,4-benzodioxin-6-carboxaldehyde (d) 1,3-Benzodioxole-5-carboxaldehyde (e) 3-Methylbenzaldehyde ... A

Synthesize Find similar

107

Synthesize Find similar Rx-ID: 8636934 Find similar reactions

A: 32% B: 38%

With silica FSM-16 in acetone

T=20°C; Oxidation; UV-irradiation;

Itoh, Akichika; Kodama, Tomohiro; Inagaki, Shinji; Masaki, Yukio

Organic Letters, 2000 , vol. 2, # 16 p. 2455 - 2457 Title/Abstract Full Text View citing articles Show Details

108

Synthesize Find similar 96%

With triethylene diamine nickel thiosulfate; water in chloroform

T=20°C; Hydrolysis; 0.0833333 h;

Synthesize Find similar

Rx-ID: 8680804 Find similar reactions

Kamal; Arifuddin; Rao

Synlett, 2000 , # 10 p. 1482 - 1484 Title/Abstract Full Text View citing articles Show Details

109

Synthesize Find similar

Rx-ID: 2296125 Find similar reactions

100%

With ammonium cerium(IV) nitrate in methanol; water

T=20°C; Ring cleavage; 0.166667 h;

Nair, Vijay; Nair, Latha G.; Balagopal, Lakshmi; Rajan, Roshini

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999 , vol. 38, # 11 p. 1234 - 1236 Title/Abstract Full Text View citing articles Show Details

95%

With dimethylboron bromide in dichloromethane; 1,2dichloro-ethane

T=-78°C; 1 h;

Quindon, Yvan; Morton, Howard E.; Yoakim, Christiane

Tetrahedron Letters, 1983 , vol. 24, # 37 p. 3969 - 3972 Title/Abstract Full Text View citing articles Show Details

With dimethylboron bromide; sodium hydrogencarbonate

1) CH2Cl2, -78 deg C, 1h, 2) THF, 5 min; Yield given. Multistep reaction;

Guindon, Yvan; Yoakim, Christiane; Morton, Howard E.

Journal of Organic Chemistry, 1984 , vol. 49, # 21 p. 3912 - 3920 Title/Abstract Full Text View citing articles Show Details

110

Synthesize Find similar 84%

Synthesize Find similar

With ammonium cerium(IV) nitrate in water; acetonitrile

T=20°C; Oxidation; 70 h;

Rx-ID: 5268853 Find similar reactions

Giurg, Miroslaw; Mlochowski, Jacek

Synthetic Communications, 1999 , vol. 29, # 24 p. 4307 - 4313 Title/Abstract Full Text View citing articles Show Details

111

Synthesize Find similar 85%

Rx-ID: 8501356 Find similar reactions

With potassium hydroxide in tetrahydrofuran; water

48 h; Ambient temperature;

Nakamura, Hiroyuki; Aoyagi, Kouichi; Yamamoto, Yoshinori

Journal of Organometallic Chemistry, 1999 , vol. 574, # 1 p. 107 - 115

Title/Abstract Full Text View citing articles Show Details

112

Synthesize Find similar With sodium hydroxide; diisobutylaluminium hydride

1.) toluene, CH2Cl2, 0 deg C, 10 min; 2.) MeOH, room temp.; Yield given. Multistep reaction;

Synthesize Find similar

Rx-ID: 4891373 Find similar reactions

Arai, Eri; Tokuyama, Hidetoshi; Linsell, Martin S.; Fukuyama, Tohru

Tetrahedron Letters, 1998 , vol. 39, # 1-2 p. 71 - 74 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

113

Synthesize Find similar Rx-ID: 4854168 Find similar reactions

With oxygen; vanadium pentaoxide; antimony trioxide; Titanium(IV) oxide in water

T=390°C; P=750.06 Torr; other temperatures; Product distribution;

Antol, Marcel; Cvengrosova, Zuzana; Vrabel, Imrich; Lesko, Jan; Hronec, Milan

Collection of Czechoslovak Chemical Communications, 1997 , vol. 62, # 9 p. 1481 - 1490 Title/Abstract Full Text View citing articles Show Details

114

Synthesize Find similar 64%

With toluene-4-sulfonic acid in acetonitrile

T=90°C; 0.333333 h;

Synthesize Find similar

Rx-ID: 4902471 Find similar reactions

Naka, Hiroyuki; Sato, Soichi; Horn, Ernst; Furukawa, Naomichi

Heterocycles, 1997 , vol. 46, # 1 p. 177 - 184 Title/Abstract Full Text View citing articles Show Details

115

Synthesize Find similar

Rx-ID: 4343145 Find similar reactions

63%

Synthesize Find similar

With aluminium trichloride in dichloromethane

T=-78°C; 4 h;

Synthesize Find similar

Niestroj, Michael; Neumann, Wilhelm P.

Chemische Berichte, 1996 , vol. 129, # 1 p. 45 - 51 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

116

Synthesize Find similar Rx-ID: 4423273 Find similar reactions

A: 4% B: 2% C: 2%

With methyltrioxorhenium (VII) in benzene

48 h; Ambient temperature;

Zhu, Zuolin; Espenson, James H.

Journal of Organic Chemistry, 1996 , vol. 61, # 1 p. 324 - 328 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

117

Synthesize Find similar Rx-ID: 4453090 Find similar reactions

T=15°C; 24 h; Irradiationother wavelength upon irradiation; also in solution (MeCN); Product distributionQuantum yield;

Koshima, Hideko; Ding, Kuiling; Chisaka, Yosuke; Matsuura, Teruo; Ohashi, Yuji; Mukasa, Manabu

Journal of Organic Chemistry, 1996 , vol. 61, # 7 p. 2352 - 2357 Title/Abstract Full Text View citing articles Show Details

118

Synthesize Find similar With 2-Bromo-1,3,5-trimethylbenzene; triphenylphosphine in water; N,N-dimethylformamide; acetone

T=120°C; 4 h; Yield given;

Synthesize Find similar

Rx-ID: 4471642 Find similar reactions

Wilson, Noel S.; Keay, Brian A.

Journal of Organic Chemistry, 1996 , vol. 61, # 9 p. 2918 - 2919 Title/Abstract Full Text View citing articles Show Details

119

Synthesize Find similar With 2,2,2-trifluoroethanol

T=20°C; other nucleophiles; Rate constant;

Synthesize Find similar

Rx-ID: 4585910 Find similar reactions

Kirmse, Wolfgang; Guth, Michael; Steenken, Steen

Journal of the American Chemical Society, 1996 , vol. 118, # 44 p. 10838 - 10849 Title/Abstract Full Text View citing articles Show Details

120

Synthesize Find similar Multi-step reaction with 2 steps 1: 73 percent / PdCl2(CH3CN)2 / acetone; H2O / 16 h / 75 °C 2: Ph3P, 2-bromomesitylene / acetone; dimethylformamide; H2O / 4 h / 120 °C View Scheme

Synthesize Find similar

Rx-ID: 17825241 Find similar reactions

Wilson, Noel S.; Keay, Brian A.

Journal of Organic Chemistry, 1996 , vol. 61, # 9 p. 2918 - 2919 Title/Abstract Full Text View citing articles Show Details

121

Synthesize Find similar Rx-ID: 4158953 Find similar reactions

With sodium carbonate; adogen 464; palladium dichloride in 1,2-dichloro-ethane

22 h; Heating; Yield given. Yields of byproduct given. Title compound not separated from byproducts;

Synthesize Find similar

Ait-Mohand; Henin; Muzart

Tetrahedron Letters, 1995 , vol. 36, # 14 p. 2473 - 2476 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

122

Synthesize Find similar

Rx-ID: 4177676 Find similar reactions

With sodium carbonate; adogen 464; palladium dichloride

22 h; Heating; Yield given. Yields of byproduct given;

Ait-Mohand; Henin; Muzart

Tetrahedron Letters, 1995 , vol. 36, # 14 p. 2473 - 2476 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

123

Synthesize Find similar Rx-ID: 4295653 Find similar reactions

A: 2% B: 8% C: 51%

With sodium percarbonate; adogen 464; bis-(tributyltin oxide) dioxochromium(VI); toluene-4-sulfonic acid in acetonitrile

20 h; Heating;

Muzart, Jacques; Aiet-Mohand, Samia

Tetrahedron Letters, 1995 , vol. 36, # 32 p. 5735 - 5736 Title/Abstract Full Text View citing articles Show Details

A: 2% B: 8% C: 51%

With sodium percarbonate; adogen 464; bis-(tributyltin oxide) dioxochromium(VI); toluene-4-sulfonic acid in acetonitrile

20 h; Heating;

Muzart, Jacques; Aiet-Mohand, Samia

Tetrahedron Letters, 1995 , vol. 36, # 32 p. 5735 - 5736 Title/Abstract Full Text View citing articles Show Details

A: 2% B: 8% C: 51%

With sodium percarbonate; adogen 464; bis-(tributyltin oxide) dioxochromium(VI); toluene-4-sulfonic acid in acetonitrile

20 h; Heating;

Muzart, Jacques; Aiet-Mohand, Samia

Tetrahedron Letters, 1995 , vol. 36, # 32 p. 5735 - 5736 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

124

Synthesize Find similar Rx-ID: 4344354 Find similar reactions

With Co(acetylacetonate)3; oxygen in tetrahydrofuran

T=70°C; 24 h; Yield given. Yields of byproduct given;

Reetz, Manfred T.; Toellner, Karl

Tetrahedron Letters, 1995 , vol. 36, # 52 p. 9461 - 9464 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

125

Synthesize Find similar Rx-ID: 2204896 Find similar reactions

in acetonitrile

17 h; Irradiationradiolysis by 1.4 mR of radiation from a 60Co source; with/without Et3N reagent; Product distributionRate constant;

Guthrie, Robert D.; Patwardhan, Manjiri; Chateauneuf, John E.

Journal of Physical Organic Chemistry, 1994 , vol. 7, # 3 p. 147 - 152 Title/Abstract Full Text Show Details

126

Synthesize Find similar Rx-ID: 3680365 Find similar reactions

Synthesize Find similar

With 3-chloro-benzenecarboperoxoic acid in dichloromethane

T=25°C; Yield given. Yields of byproduct given;

Sakanishi, Katsumasa; Nugroho, Mohamed Bambang; Kato, Yoshiyuki; Yamazaki, Natsuki

Tetrahedron Letters, 1994 , vol. 35, # 21 p. 3559 - 3562 Title/Abstract Full Text View citing articles Show Details

With 3,3-dimethyldioxirane in dichloromethane; acetone

T=25°C; ΔG(excit.); ΔH(excit.); ΔS(excit.); different reagents and temperatures; Rate constantThermodynamic data;

Sakanishi, Katsumasa; Kato, Yoshiyuki; Mizukoshi, Emi; Shimizu, Kazufumi

Tetrahedron Letters, 1994 , vol. 35, # 27 p. 4789 - 4792 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

127

Synthesize Find similar Rx-ID: 8492389 Find similar reactions

128

With 3-chloro-benzenecarboperoxoic acid in dichloromethane

T=25°C; ΔG(excit), ΔH(excit), ΔS(excit); reactions of derivatives under var. conditions; KineticsRate constantThermodynamic data;

Sakanishi, Katsumasa; Nugroho, Mohamed Bambang; Kato, Yoshiyuki; Yamazaki, Natsuki

Tetrahedron Letters, 1994 , vol. 35, # 21 p. 3559 - 3562 Title/Abstract Full Text View citing articles Show Details

With 3-chloro-benzenecarboperoxoic acid in dichloromethane

T=25°C; reactions of derivatives under var. conditions; Mechanism;

Sakanishi, Katsumasa; Nugroho, Mohamed Bambang; Kato, Yoshiyuki; Yamazaki, Natsuki

Tetrahedron Letters, 1994 , vol. 35, # 21 p. 3559 - 3562 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar Multi-step reaction with 2 steps 1: N-bromosuccinimide, benzoyl peroxide / benzene / 2 h / Heating 2: MeONa, 2-nitropropane / methanol / 7 h / 20 - 40 °C View Scheme

Synthesize Find similar

Rx-ID: 18380391 Find similar reactions

Hashizume; Ito; Yamada; Nagashima; Kanao; Tomoda; Sunazuka; Kumagai; Omura

Chemical and pharmaceutical bulletin, 1994 , vol. 42, # 3 p. 512 - 520 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

129

Synthesize Find similar Rx-ID: 3454222 Find similar reactions

With sodium carbonate; 3-chloro-benzenecarboperoxoic acid in chloroform

T=-10°C; 5 h; Yield given;

Mlochowski, J.; Abdel-Latif, F. F.; Kubicz, E.; Said, S. B.

Polish Journal of Chemistry, 1993 , vol. 67, # 4 p. 711 - 722 Title/Abstract Full Text Show Details

Synthesize Find similar

130

Synthesize Find similar Rx-ID: 2176366 Find similar reactions

A: 33% B: 34%

With 9,10-anthracenedicarbonitrile; oxygen in acetonitrile

1.5 h; Irradiation;

Tamai, Toshiyuki; Mizuno, Kazuhiko; Hashida, Isao; Otsuji, Yoshio

Chemistry Letters, 1992 , # 5 p. 781 - 784 Title/Abstract Full Text Show Details

A: 33% B: 34%

With 9,10-anthracenedicarbonitrile; oxygen in acetonitrile

1.5 h; Irradiation;

Tamai, Toshiyuki; Mizuno, Kazuhiko; Hashida, Isao; Otsuji, Yoshio

Chemistry Letters, 1992 , # 5 p. 781 - 784 Title/Abstract Full Text Show Details

Synthesize Find similar

131

Synthesize Find similar Rx-ID: 3223862 Find similar reactions

in water

T=25°C; Equilibrium constant;

Stachissini, Antonia Sonia; Amaral, Antonia T. do; Amaral, Luciano do

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1992 , # 11 p. 1929 - 1931 Title/Abstract Full Text View citing articles Show Details

132

Synthesize Find similar With pyridine; lithiumtris(diethylamino)hydridoaluminate in tetrahydrofuran

T=0°C; Reduction; 0.5 h;

Synthesize Find similar

Rx-ID: 5253196 Find similar reactions

Cha, Jin Soon; Lee, Jae Cheol Lee; Lee, Sung Eun

Organic Preparations and Procedures International, 1992 , vol. 24, # 3 p. 327 - 330 Title/Abstract Full Text Show Details

133

Synthesize Find similar Multi-step reaction with 2 steps 1: tetrahydrofuran / 20 °C 2: Li(Et2N)3AlH; pyridine / tetrahydrofuran / 0.5 h / 0 °C View Scheme

Synthesize Find similar

Rx-ID: 16209591 Find similar reactions

Cha, Jin Soon; Lee, Jae Cheol Lee; Lee, Sung Eun

Organic Preparations and Procedures International, 1992 , vol. 24, # 3 p. 327 - 330 Title/Abstract Full Text Show Details

Synthesize Find similar

134

Synthesize Find similar

Rx-ID: 1784018 Find similar reactions

With hydrogen fluoride; SbF5

T=0°C; P=15200 Torr; 3 h; other polynuclear aromatic compounds; var reaction conditions; Product distribution;

Tanaka; Souma

Journal of the Chemical Society - Series Chemical Communications, 1991 , # 21 p. 1551 - 1553 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

135

Synthesize Find similar Rx-ID: 3864276 Find similar reactions

A: 3.5% B: 61%

With hydrogen; triethylamine; HRhCl2(tricyclohexylphosphine)2 in benzene

T=50°C; P=760 Torr; 65 h;

Grushin, Vladimir V.; Alper, Howard

Journal of Organic Chemistry, 1991 , vol. 56, # 17 p. 5159 - 5161 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

136

Synthesize Find similar Rx-ID: 3613389 Find similar reactions

in chloroform-d1

T=50°C; 45 h; further times, half life time; Rate

Doepp, Dietrich; Memarian, Hamid Reza; Krueger, Carl; Raabe, Eleonore

Chemische Berichte, 1989 , vol. 122, p. 585 - 588

constantProduct distribution;

Title/Abstract Full Text Show Details

Synthesize Find similar

137

Synthesize Find similar Rx-ID: 3624083 Find similar reactions

Seal, B. K.; Mukherjee, A. K.

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1986 , vol. 25, # 5 p. 413 - 415 Title/Abstract Full Text Show Details

T=37°C; Equilibrium constant;

Synthesize Find similar

138

Synthesize Find similar Rx-ID: 3861670 Find similar reactions

With oxygen; 2,6,9,10-tetracyanoanthracene in acetonitrile T=22°C; Irradiationphotooxidation, other sensitizers, solvents and products; Product distributionMechanismQuantum yield;

Albini, Angelo; Spreti, Silvia

Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1986 , vol. 41, # 10 p. 1286 - 1292 Title/Abstract Full Text Show Details

Synthesize Find similar

139

Synthesize Find similar Rx-ID: 1999415 Find similar reactions

Synthesize Find similar

A: 11% B: 10% C: 41% D: 11%

T=24°C; 9 h; Irradiation; Further byproducts given;

Horn, Keith A.; Chateauneuf, John E.

Tetrahedron, 1985 , vol. 41, # 8 p. 1465 - 1470 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

140

Synthesize Find similar Rx-ID: 2549623 Find similar reactions

A: 11% B: 10% C: 41% D: 11%

in cyclohexane

T=24°C; 9 h; Irradiation; Further byproducts given;

Horn, Keith A.; Chateauneuf, John E.

Tetrahedron, 1985 , vol. 41, # 8 p. 1465 - 1470 Title/Abstract Full Text View citing articles Show Details

A: 11% B: 10% C: 41% D: 11%

in cyclohexane

T=24°C; 9 h; Irradiation; Further byproducts given;

Horn, Keith A.; Chateauneuf, John E.

Tetrahedron, 1985 , vol. 41, # 8 p. 1465 - 1470 Title/Abstract Full Text View citing articles Show Details

A: 11% B: 10% C: 41% D: 11%

in cyclohexane

T=24°C; 9 h; Irradiation; Further byproducts given;

Horn, Keith A.; Chateauneuf, John E.

Tetrahedron, 1985 , vol. 41, # 8 p. 1465 - 1470 Title/Abstract Full Text View citing articles Show Details

141

Synthesize Find similar

Rx-ID: 2885159 Find similar reactions

A: 27% B: 4% C: 37%

With ammonium cerium(IV) nitrate in water

T=85°C; 2 h;

Sydnes, Leiv K.; Burkow, Ivan C.; Hansen, Sissel H.

Tetrahedron, 1985 , vol. 41, # 23 p. 5703 - 5706 Title/Abstract Full Text View citing articles Show Details

142

Synthesize Find similar Rx-ID: 3861671 Find similar reactions

Synthesize Find similar

A: 27% B: 4% C: 37%

With ammonium cerium(IV) nitrate in water; acetic acid

T=85°C; 2 h;

Sydnes, Leiv K.; Burkow, Ivan C.; Hansen, Sissel H.

Tetrahedron, 1985 , vol. 41, # 23 p. 5703 - 5706 Title/Abstract Full Text View citing articles Show Details

A: 27% B: 4% C: 37%

With ammonium cerium(IV) nitrate in water; acetic acid

T=85°C; 2 h;

Sydnes, Leiv K.; Burkow, Ivan C.; Hansen, Sissel H.

Tetrahedron, 1985 , vol. 41, # 23 p. 5703 - 5706 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

143

Synthesize Find similar

Rx-ID: 2506714 Find similar reactions

100%

With tetrafluoroboric acid; mercury(II) oxide in tetrahydrofuran

Ambient temperature;

Degani, Iacopo; Fochi, Rita; Regondi, Valeria

Synthesis, 1981 , # 1 p. 51 - 53 Title/Abstract Full Text Show Details

100%

With tetrafluoroboric acid; mercury(II) oxide in tetrahydrofuran

Ambient temperaturevarious 1,3-dithiolanes; Product distribution;

Degani, Iacopo; Fochi, Rita; Regondi, Valeria

Synthesis, 1981 , # 1 p. 51 - 53 Title/Abstract Full Text Show Details

99.6%

With K-10 clay supported copper(II) nitrate trihydrate in dichloromethane

6 h; Ambient temperaturewith K-10 clay-supported iron(III) nitrate nonahydrate;

Balogh, Maria; Cornelis, Andre; Laszlo, Pierre

Tetrahedron Letters, 1984 , vol. 25, # 31 p. 3313 - 3316 Title/Abstract Full Text View citing articles Show Details

99.6%

With K-10 clay supported copper(II) nitrate trihydrate in dichloromethane

6 h; Ambient temperatureK-10 clay supported iron(III) nitrate nonahydrate;

Balogh, Maria; Cornelis, Andre; Laszlo, Pierre

Tetrahedron Letters, 1984 , vol. 25, # 31 p. 3313 - 3316 Title/Abstract Full Text View citing articles Show Details

144

Synthesize Find similar

Rx-ID: 3861672 Find similar reactions

A: 19 % Chromat. C: 54 % Chromat.

With 9,10-anthracenedicarbonitrile; oxygen in acetonitrile

Irradiation;

Synthesize Find similar

Santamaria, J.; Gabillet, P.; Bokobza, L.

Tetrahedron Letters, 1984 , vol. 25, # 20 p. 2139 - 2142 Title/Abstract Full Text View citing articles Show Details

145

Synthesize Find similar

Rx-ID: 1538228 Find similar reactions

34 % Chromat.

in acetonitrile

T=80°C; 3 h; Irradiation;

Synthesize Find similar

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Pierre

Bulletin de la Societe Chimique de France, 1982 , vol. 2, # 7-8 p. 262 - 264 Title/Abstract Full Text Show Details

Synthesize Find similar

146

Synthesize Find similar Rx-ID: 1538229 Find similar reactions

A: 34 % Chromat. B: 16 % Chromat.

in acetonitrile

T=80°C; 3 h; Irradiation;

Synthesize Find similar

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Pierre

Bulletin de la Societe Chimique de France, 1982 , vol. 2, # 7-8 p. 262 - 264 Title/Abstract Full Text Show Details

Synthesize Find similar

147

Synthesize Find similar

Rx-ID: 1538240 Find similar reactions

A: 34 % Chromat. B: 38 % Chromat.

in acetonitrile

2 h; Irradiation;

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Pierre

Bulletin de la Societe Chimique de France, 1982 , vol. 2, # 7-8 p. 262 - 264 Title/Abstract Full Text Show Details

A: 34 % Chromat. B: 38 % Chromat.

in acetonitrile

2 h; Irradiation;

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Pierre

Bulletin de la Societe Chimique de France, 1982 , vol. 2, # 7-8 p. 262 - 264 Title/Abstract Full Text Show Details

Synthesize Find similar

148

Synthesize Find similar Rx-ID: 2627866 Find similar reactions

A: 2% B: 13% C: 11% D: 17%

With dihydrogen peroxide in tetrahydrofuran

Further byproducts given;

Pomerantz, Martin; Swei, Gwo-Shin

Tetrahedron Letters, 1982 , vol. 23, # 30 p. 3027 - 3030 Title/Abstract Full Text View citing articles Show Details

Synthesize

149

Synthesize Find similar

Rx-ID: 2627867 Find similar reactions

A: 2% B: 11% C: 17% D: 4%

With dihydrogen peroxide in tetrahydrofuran

Further byproducts given;

Find similar

Synthesize Find similar

Pomerantz, Martin; Swei, Gwo-Shin

Tetrahedron Letters, 1982 , vol. 23, # 30 p. 3027 - 3030 Title/Abstract Full Text View citing articles Show Details

150

Synthesize Find similar

Rx-ID: 6217786 Find similar reactions

With cobalt acetate tetrahydrate

T=60°C; 1 h; other temperature; MechanismProduct distribution;

Baciocchi, Enrico; Rol, Cesare; Sebastiani, Giovanni V.

Gazzetta Chimica Italiana, 1982 , vol. 112, # 11/12 p. 513 - 518 Title/Abstract Full Text Show Details

Synthesize Find similar

151

Synthesize Find similar Rx-ID: 1751775 Find similar reactions

A: 3.5 % Chromat. B: 1 % Chromat. C: 0.7%

in cyclohexane

T=20°C; 8 h; Irradiation;

Zander, Maximilian

Chemische Berichte, 1981 , vol. 114, # 7 p. 2665 - 2667 Title/Abstract Full Text Show Details

152

Synthesize Find similar Rx-ID: 1821788 Find similar reactions

B: 20%

in acetonitrile

4 h; Ambient temperatureIrradiation; Product distributionMechanism;

Synthesize Find similar

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Piere

Journal of Organic Chemistry, 1981 , vol. 46, # 21 p. 4275 - 4279 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

153

Synthesize Find similar Rx-ID: 1828498 Find similar reactions

A: 9% B: 13%

in cyclohexane

1.5 h; Ambient temperatureIrradiationother solvents; Product distributionMechanism;

Hallet, Philippe; Muzart, Jacques; Pete, Jean-Piere

Journal of Organic Chemistry, 1981 , vol. 46, # 21 p. 4275 - 4279 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

154

Synthesize Find similar Rx-ID: 3556860 Find similar reactions

A: 5% B: 6% C: 44%

With sodium hydroxide; cobalt trricarbonyl nitrosyl; ndodecyltrimethylammonium chloride in benzene

P=760 Torr; Ambient temperature;

Synthesize Find similar

Gambarotta, Sandro; Alper, Howard

Journal of Organometallic Chemistry, 1981 , vol. 212, # 1 p. C23 - C26 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

155

Synthesize Find similar Rx-ID: 3556929 Find similar reactions

A: 5% B: 6% C: 44%

With sodium hydroxide; cobalt trricarbonyl nitrosyl; carbon monoxide; n-dodecyltrimethylammonium chloride in benzene

P=760 Torr; Ambient temperature;

Gambarotta, Sandro; Alper, Howard

Journal of Organometallic Chemistry, 1981 , vol. 212, # 1 p. C23 - C26 Title/Abstract Full Text View citing articles Show Details

A: 5% B: 6% C: 44%

With sodium hydroxide; cobalt trricarbonyl nitrosyl; carbon monoxide; n-dodecyltrimethylammonium chloride in benzene

P=760 Torr; Ambient temperature;

Gambarotta, Sandro; Alper, Howard

Journal of Organometallic Chemistry, 1981 , vol. 212, # 1 p. C23 - C26 Title/Abstract Full Text View citing articles Show Details

156

Synthesize Find similar 87%

With benzeneseleninic anhydride in tetrahydrofuran

T=40 - 50°C; 0.5 h;

Synthesize Find similar

Rx-ID: 1453687 Find similar reactions

Barton, Derek H. R.; Lester, David J.; Ley, Steven V.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 1212 - 1217 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

157

Synthesize Find similar Rx-ID: 2824039 Find similar reactions

A: 0.09 g

in cyclohexane

3 h; Irradiation;

Veierov, Dan; Mazur, Yehuda; Fischer, Ernst

Journal of the Chemical Society, Perkin Transactions 2, 1980 , # 11 p. 1659 - 1664 Title/Abstract Full Text View citing articles Show Details

in hexane

T=0°C; Irradiationseveral concentrations, solvents, irradiation intensities, reaction times, wavelenghts; Quantum yieldMechanismProduct distribution;

Veierov, Dan; Mazur, Yehuda; Fischer, Ernst

Journal of the Chemical Society, Perkin Transactions 2, 1980 , # 11 p. 1659 - 1664 Title/Abstract Full Text View citing articles Show Details

Synthesize Find similar

158

Synthesize Find similar Rx-ID: 3002397 Find similar reactions

A: 30 mg B: 25 mg C: 15 mg D: 250 mg

in hexane

T=0°C; Irradiationvariation of wavelenght, concentration, solvent, irradiation intensity, reaction time; Quantum yieldMechanismProduct distribution;

Veierov, Dan; Mazur, Yehuda; Fischer, Ernst

Journal of the Chemical Society, Perkin Transactions 2, 1980 , # 11 p. 1659 - 1664 Title/Abstract Full Text View citing articles Show Details

in cyclohexane

2 h; Irradiation;

Veierov, Dan; Mazur, Yehuda; Fischer, Ernst

Journal of the Chemical Society, Perkin Transactions 2, 1980 , # 11 p. 1659 - 1664 Title/Abstract Full Text View citing articles Show Details

159

Synthesize Find similar

Rx-ID: 132246 Find similar reactions

With hydrogenchloride; diethyl ether; tin(ll) chloride

Erhitzen des Reaktionsprodukts mit Wasserdampf;

Fulton; Robinson

Journal of the Chemical Society, 1939 , p. 200 Full Text Show Details

Sah

Recueil des Travaux Chimiques des Pays-Bas, 1940 , vol. 59, p. 461,468, 1021, 1026 Full Text View citing articles Show Details

Williams

Journal of the American Chemical Society, 1939 , vol. 61, p. 2248 Organic Syntheses, 1955 , vol. Coll. Vol. III, p. 626 Full Text View citing articles Show Details

With ethanol; water; nickel

Hydrogenation.weiteres Reagens: Essigester;

Rupe; Becherer

Helvetica Chimica Acta, 1923 , vol. 6, p. 882 Full Text View citing articles Show Details

With lithium aluminium tetrahydride

Braude; Gore

Journal of the Chemical Society, 1959 , p. 41,46 Full Text View citing articles Show Details

With sodium triethoxyalanate

Hesse; Schroedel

Justus Liebigs Annalen der Chemie, 1957 , vol. 607, p. 24,30 Full Text Show Details

160

Synthesize Find similar

Rx-ID: 5855807 Find similar reactions

Evans

Chemistry and Industry (London, United Kingdom), 1957 , p. 1596 Full Text View citing articles Show Details

161

Synthesize Find similar With 4-(N,N-diethylamino)-toluene

Synthesize Find similar

Rx-ID: 398537 Find similar reactions

Cymerman-Craig et al.

Australian Journal of Chemistry, 1956 , vol. 9, p. 222,226 Full Text Show Details

162

Synthesize

Find similar Rx-ID: 724801 Find similar reactions

With copper(II) sulfate; sodium sulfite

Diazotization;

Find similar

Beech

Journal of the Chemical Society, 1954 , p. 1297,1300 Full Text View citing articles Show Details

163

Synthesize Find similar

Rx-ID: 5855808 Find similar reactions

Sah; Bruell; Holzen

Chemische Berichte, 1940 , vol. 73, p. 762 Full Text View citing articles Show Details

164

Synthesize Find similar

Rx-ID: 5855813 Find similar reactions

Sah

Recueil des Travaux Chimiques des Pays-Bas, 1940 , vol. 59, p. 1029,1034 Full Text View citing articles Show Details

165

Synthesize Find similar With water

T=140 - 150°C;

Synthesize Find similar

Rx-ID: 456899 Find similar reactions

Achmatowicz; Lindenfeld

Roczniki Chemii, 1938 , vol. 18, p. 69,72 Chem. Zentralbl., 1939 , vol. 110, # II p. 389

Full Text View citing articles Show Details

166

Synthesize Find similar

Rx-ID: 8255536 Find similar reactions

T=140 - 145°C;

Synthesize Find similar

Achmatowicz; Lindenfeld

Roczniki Chemii, 1938 , vol. 18, p. 69,72 Chem. Zentralbl., 1939 , vol. 110, # II p. 389 Full Text View citing articles Show Details

167

Synthesize Find similar With hydrogenchloride

Rx-ID: 5855812 Find similar reactions

Wuyts; Berman; Lacourt

Bulletin des Societes Chimiques Belges, 1931 , vol. 40, p. 665,669 Full Text View citing articles Show Details

168

Synthesize Find similar With ammonium hydroxide; potassium hexacyanoferrate(III)

Synthesize Find similar

Rx-ID: 291321 Find similar reactions

Kalb; Gross

Chemische Berichte, 1926 , vol. 59, p. 733 Full Text View citing articles Show Details

169

Synthesize Find similar

Rx-ID: 291322 Find similar reactions

With ammonium hydroxide; potassium hexacyanoferrate(III)

Synthesize Find similar

Kalb; Gross

Chemische Berichte, 1926 , vol. 59, p. 733 Full Text View citing articles Show Details

170

Synthesize Find similar

With phosphorus pentachloride; tetrachloroethane, 1,1,2,2T=140 - 150°C; Eintragen des Reaktionsprodukts in eine mit Chlorwasserstoff gesaettigte aetherische Loesung von Zinn(II)-chlorid und Destillieren mit Wasserdampf;

Rx-ID: 395551 Find similar reactions

Gibson et al.

Journal of the Chemical Society, 1926 , p. 2253 Full Text View citing articles Show Details

Synthesize Find similar

171

Synthesize Find similar

Rx-ID: 7445154 Find similar reactions

Kalb; Gross

Chemische Berichte, 1926 , vol. 59, p. 733 Full Text View citing articles Show Details

172

Synthesize Find similar

Rx-ID: 6726436 Find similar reactions

Hydrogenation;

Synthesize Find similar

Rupe; Becherer

Helvetica Chimica Acta, 1923 , vol. 6, p. 882 Full Text View citing articles Show Details

Rupe

Patent: DE429042 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 15, p. 328 Full Text Show Details

173

Synthesize Find similar Multi-step reaction with 2 steps 1: durch Destillation 2: nickel; water; alcohol / Hydrogenation.weiteres Reagens: Essigester View Scheme

Synthesize Find similar

Rx-ID: 22059585 Find similar reactions

Rupe; Becherer

Helvetica Chimica Acta, 1923 , vol. 6, p. 882 Full Text View citing articles Show Details

174

Synthesize Find similar

Rx-ID: 301073 Find similar reactions

Synthesize Find similar

Mayer,F.; Sieglitz

Chemische Berichte, 1922 , vol. 55, p. 1854 Full Text View citing articles Show Details

Synthesize Find similar

175

Synthesize Find similar

Rx-ID: 6681948 Find similar reactions

Synthesize Find similar

Weil; Ostermeier

Chemische Berichte, 1921 , vol. 54, p. 3218 Full Text View citing articles Show Details

Weil

Chemische Berichte, 1911 , vol. 44, p. 3060 Full Text Show Details

176

Synthesize Find similar

Rx-ID: 796089 Find similar reactions

Synthesize Find similar

Gattermann

Justus Liebigs Annalen der Chemie, 1912 , vol. 393, p. 224 Full Text View citing articles Show Details

Monier-Williams

Journal of the Chemical Society, 1906 , vol. 89, p. 275 Full Text View citing articles Show Details

Zersetzung des Reaktionsproduktes mit verd. Salzsaeure;

177

Monier-Williams

Journal of the Chemical Society, 1906 , vol. 89, p. 275 Full Text View citing articles Show Details

Synthesize Find similar

Rx-ID: 699725 Find similar reactions

With diethyl ether

Synthesize Find similar

Tschitschibabin

Chemische Berichte, 1911 , vol. 44, p. 442 Full Text View citing articles Show Details

178

Synthesize Find similar With lead (II) nitrate

Rx-ID: 5855805 Find similar reactions

Kikkoji

Biochemische Zeitschrift, 1911 , vol. 35, p. 67 Full Text View citing articles Show Details

Schulze

Chemische Berichte, 1884 , vol. 17, p. 1530 Full Text View citing articles Show Details

179

Synthesize Find similar durch Destillation;

180

Synthesize Find similar

Rx-ID: 5855806 Find similar reactions

Behrend; Ludewig

Justus Liebigs Annalen der Chemie, 1911 , vol. 379, p. 355 Full Text View citing articles Show Details

Battershall

Justus Liebigs Annalen der Chemie, 1873 , vol. 168, p. 116 Full Text View citing articles Show Details

Synthesize Find similar

Rx-ID: 5855804 Find similar reactions

durch Verseifung, Erhitzen der Saeure mit Anilin und Zersetzen des entstandenen Anils durch verd. Schwefelsaeure;

Rousset

Bulletin de la Societe Chimique de France, 1897 , vol. <3> 17, p. 309 Full Text View citing articles Show Details

181

Synthesize Find similar With lead (II) nitrate

Rx-ID: 5855802 Find similar reactions

Schulze

Chemische Berichte, 1884 , vol. 17, p. 1530 Full Text View citing articles Show Details

182

Synthesize Find similar With lead (II) nitrate

Rx-ID: 5855803 Find similar reactions

Schulze

Chemische Berichte, 1884 , vol. 17, p. 1530 Full Text View citing articles Show Details

183

Synthesize Find similar

Rx-ID: 5855810 Find similar reactions

Schulze

Chemische Berichte, 1884 , vol. 17, p. 1530 Full Text View citing articles Show Details

184

Synthesize Find similar

Rx-ID: 5855811 Find similar reactions

Schulze

Chemische Berichte, 1884 , vol. 17, p. 1530 Full Text View citing articles Show Details

185

Synthesize Find similar

durch Destillation;

Rx-ID: 5855809 Find similar reactions

Battershall

Justus Liebigs Annalen der Chemie, 1873 , vol. 168, p. 116 Full Text View citing articles Show Details

Synthesize Find similar

186

Synthesize Find similar Rx-ID: 8255537 Find similar reactions

Synthesize Find similar

Battershall

Justus Liebigs Annalen der Chemie, 1873 , vol. 168, p. 116 Full Text View citing articles Show Details

187

Synthesize Find similar Rx-ID: 8255538 Find similar reactions

Synthesize Find similar

Battershall

Justus Liebigs Annalen der Chemie, 1873 , vol. 168, p. 116 Full Text View citing articles Show Details

Synthesize Find similar