68523-24-0 = 86-79-3 反应条件:1.1 Catalysts: Tripotassium Phosphate Solvents: Methanol; 10 H,30 °C 标题:A Photochemical Synthesis Of 2-Hydroxycarbazole 作者:Liu,Rui; Et Al 参考文献:Zhejiang Gongye Daxue Xuebao 日期:2012 卷标:40(4) 页码:405-407]
76834-74-7 = 86-79-3 [标题:Reaction Conditions 标题:Flash-Vacuum Pyrolysis Of 5-(Indol-2- And -3-Ylmethylene)-2,2-Dimethyl-1,3-Dioxane-4,6-Diones 作者:Banzies,David W. M.; Et Al 参考文献:Journal Of The Chemical Society 日期:1986 卷标:(9) 页码:1651-4]
16098-16-1 = 86-79-3 反应条件:1.1 Reagents: Boron Tribromide Solvents: Dichloromethane; 5 H,Rt2.1 Catalysts: 1,10-Phenanthroline,Disodium Tetrachloropalladate Solvents: Dimethylformamide; 10 Min,Rt2.2 Reagents: Phenyl Formate,Trisodium Phosphate; 5 H,170 °C2.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47]
2033-24-1 + 5416-80-8 = 86-79-3 反应条件:1.1 Reagents: Benzene,Piperidine Solvents: Benzene2.1 - 标题:Flash-Vacuum Pyrolysis Of 5-(Indol-2- And -3-Ylmethylene)-2,2-Dimethyl-1,3-Dioxane-4,6-Diones 作者:Banzies,David W. M.; Et Al 参考文献:Journal Of The Chemical Society 日期:1986 卷标:(9) 页码:1651-4]
99847-12-8 = 86-79-3 反应条件:1.1 Catalysts: 1,10-Phenanthroline,Disodium Tetrachloropalladate Solvents: Dimethylformamide; 10 Min,Rt1.2 Reagents: Phenyl Formate,Trisodium Phosphate; 5 H,170 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Reflux2.1 Reagents: Sodium Hydroxide Solvents: Ethanol,Water; 16 H,Reflux; Reflux -> Rt2.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Rt 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47]
51264-59-6 = 86-79-3 + 65975-66-8 反应条件:1.1 Reagents: Triphenylphosphine Catalysts: Dichlorobis(N,N-Dimethylformamide-Ko)Dioxomolybdenum Solvents: Toluene; 16 H,Reflux 标题:Dioxomolybdenum(Vi)-Catalyzed Reductive Cyclization Of Nitroaromatics. Synthesis Of Carbazoles And Indoles 作者:Sanz,Roberto; Et Al 参考文献:Advanced Synthesis & Catalysis 日期:2007 卷标:349 页码:713-718]
13314-79-9 = 86-79-3 反应条件:1.1 Catalysts: Palladium Solvents: 2-Ethylhexanol; 4 H,180 °C; 180 °C -> 50 °C; 50 °C -> Rt1.2 Solvents: Dichloromethane; Rt; 5 H,Rt 标题:Process For Obtaining High-Purity 2-Hydroxycarbazole By Treating The Impure Compound With Oxygen-Containing Solvents And/or Halogenated Solvents 参考文献:Poland]
51094-28-1 = 86-79-3 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Ethanol,Water; 16 H,Reflux; Reflux -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Rt 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47]
51264-59-6 = 86-79-3 反应条件:1.1 Catalysts: 1,10-Phenanthroline,Disodium Tetrachloropalladate Solvents: Dimethylformamide; 10 Min,Rt1.2 Reagents: Phenyl Formate,Trisodium Phosphate; 5 H,170 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47]
= 86-79-3 反应条件:1.1 Reagents: P-Toluenesulfonic Acid Solvents: 1,4-Dioxane; Reflux 标题:The Pummerer Reaction Of Sulfinyl Compounds 作者:De Lucchi,Ottorino; Et Al 参考文献:Organic Reactions (Hoboken 日期:1991 卷标:40]
1429337-46-1 = 86-79-3 反应条件:1.1 Reagents: Sodium Azide Catalysts: Cuprous Iodide (Amberlyst A21-Supported),Amberlyst A 21 Solvents: Dimethylformamide; 48 H,150 °C 标题:Recyclable Copper Catalyzed Nitrogenation Of Biphenyl Halides: A Direct Approach To Carbazoles 作者:Ou,Yang; Et Al 参考文献:Chemical Communications (Cambridge 日期:2013 卷标:49(33) 页码:3473-3475]
103628-66-6 = 86-79-3 [标题:Reaction Conditions 标题:Procedure For Preparing 2-Hydroxy-5,6,7,8-Tetrahydrocarbazole And Its Alkali And Alkaline Earth Salts And Their Use 参考文献:Federal Republic Of Germany]
99970-47-5 = 86-79-3 [标题:Reaction Conditions 标题:Product Class 15: Carbazoles 作者:Gallagher,P. T. 参考文献:Science Of Synthesis 日期:2001 卷标:10 页码:693-744]
39180-36-4 = 86-79-3 反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Methanol; 16 H,Rt2.1 Catalysts: 1,10-Phenanthroline,Disodium Tetrachloropalladate Solvents: Dimethylformamide; 10 Min,Rt2.2 Reagents: Phenyl Formate,Trisodium Phosphate; 5 H,170 °C2.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Reflux3.1 Reagents: Sodium Hydroxide Solvents: Ethanol,Water; 16 H,Reflux; Reflux -> Rt3.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Rt 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47]
98-80-6 = 86-79-3 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Tetrakis(Triphenylphosphine)Palladium Solvents: Toluene,Water; 18 H,Reflux2.1 Reagents: Boron Tribromide Solvents: Dichloromethane; 5 H,Rt3.1 Catalysts: 1,10-Phenanthroline,Disodium Tetrachloropalladate Solvents: Dimethylformamide; 10 Min,Rt3.2 Reagents: Phenyl Formate,Trisodium Phosphate; 5 H,170 °C3.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified 标题:Catalytic Reductive Cyclization Of 2-Nitrobiphenyls Using Phenyl Formate As Co Surrogate: A Robust Synthesis Of 9H-Carbazoles 作者:Ramadan,Doaa R.; Et Al 参考文献:Journal Of Catalysis 日期:2022 卷标:409 页码:41-47
3-乙氧基苯基肼置于乙醇,Aniline Hydrochloride,钯,肉桂酸体系中,化学反应生成 2-羟基咔唑 参考文献:über Die Synthese Von Alkoxy-Und Oxy-Carbazole 标题:über Die Synthese Von Alkoxy-Und Oxy-Carbazole 摘要: DOI:10.1246/bcsj.11.218
专利号:US-2007197797-A1 优先权日:2005-12-30 标 题 :Compounds and methods for carbazole synthesis 发明人:HARRINGTON PETER J 权利人:HARRINGTON PETER J 摘要:Compounds having bi-cyclic structure comprising a partially unsaturated 6-carbon first cyclic moiety interconnected to a 6-carbon second cyclic moiety second via a divalent linking moiety are provided. The compounds can be used as intermediates compounds in methods for the synthesis of carbazoles and derviatives thereof, including carvedilol, and tricyclic alkylhydroxamates, which do not require Fischer indole synthetic steps. Methods of preparing the compounds having bi-cyclic structures are also provided.