共查询到20条相似文献,搜索用时 15 毫秒
1.
Ramin Ghorbani-Vaghei Zahra Toghraei-Semiromi Rahman Karimi-Nami 《Comptes Rendus Chimie》2013,16(12):1111-1117
A series of 2-amino-3-cyanopyridines were obtained from aryl aldehydes, substituted acetophenones, malononitrile and ammonium acetate in good to excellent yields by proceeding through a simple, mild and efficient procedure utilizing N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide [TBBDA] and poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) [PBBS] as catalysts. 相似文献
2.
Takumi Mizuno Manabu Matsumoto Ikuzo Nishiguchi Tsuneaki Hirashima 《Heteroatom Chemistry》1993,4(5):455-458
Urea derivatives were readily synthesized in good yields under quite mild conditions, i.e., at ambient pressure and room temperature by sulfur-assisted carbonylation of primary amines with carbon monoxide followed by oxidation of the resulting ammonium thiocarbamates with molecular oxygen. 相似文献
3.
One-pot synthesis of aryl-14H-dibenzo[a,j]xanthene and 1,8-dioxo-octahydroxanthene derivatives using montmorillonite K10 as reusable eco-friendly catalyst under solvent-free
conditions is described. 相似文献
4.
R. Ranjbar-Karimi S. Hashemi-Uderji M. Mousavi 《Journal of the Iranian Chemical Society》2011,8(1):193-197
A simple, clean and benign route to the synthesis of 2H-chromen-2-ones derivatives through one-pot condensation of ??-ketoesters and substituted phenols in the presence of 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bistetrafluoroborateis (Selectfluor? F-TEDA-BF4) as catalyst under solvent free reaction conditions was experimented. The application of ultrasonic irradiation improved the yields and reduced the reaction times. The use of selectfluor catalyst is feasible because of its stability, commercial value, easy handling, easy recovery and good activity. To extend our research, the ability of selectfluor for the synthesis of 2-aminochromene derivatives was also examined. 相似文献
5.
Brnsted acidic ionic liquids, namely 2-pyrrolidonium hydrogen sulfate, N-methyl-2-pyrrolidonium hydrogen sulfate, N-methyl-2-pyrrolidonium dihydrogen phosphate, (4-sulfobutyl)tris(4-sulfophenyl)phosphonium hydrogen sulfate, and triphenyl(propyl-3-sulfonyl)phosphonium toluenesulfonate, catalyzed efficient Pechmann condensation of phloroglucinol with β-keto ethyl/ methyl esters. 5,7-Dihydroxy-4-methylcoumarin and 5,7-dihydroxy-4-phenylcoumarin were prepared in good to excellent yields under mild, ambient, and solvent-free conditions. Pyrano[2,3-h] coumarins were then prepared by one-pot three-component reactions of 5,7-dihydroxy-4-subsituted coumarin, malononitrile, and aldehydes in the presence of catalytic amounts of Br nsted basic ionic liquids, namely 2-hydroxyethylammonium formate, 3-hydroxypropanaminium acetate, 1-butyl-3-methylimidazolium hydroxide, pyrrolidinium formate, and pyrrolidinium acetate, under thermal solvent-free conditions. The catalysts are environmentally benign and can be easily prepared, stored, and recovered without significant loss of activity. 相似文献
6.
Yan Chen Shanshan Wu Shujiang Tu Chunmei Li Feng Shi 《Journal of heterocyclic chemistry》2008,45(3):931-934
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8.
Hideaki Fujii 《Tetrahedron letters》2008,49(44):6293-6296
A dealkylation reaction of tertiary amines using chloroformate was a useful method for synthesizing morphinan derivatives without 17-substituents; however, the reaction has been applied to only the 14-hydromorphinans. In the course of the investigation of the 17-dealkylation reaction in 14-hydroxymorphinan, the novel cleavage reaction of the C16-N17 bond in the naltrexone derivative was found. A plausible reaction mechanism based on the stereoelectronic effect is presented. The examinations of dealkylation reactions in general tertiary amines ranked the tendency of cleavage as follows: benzyl > cyclopropylmethyl (CPM) ≈ allyl > methyl, ethyl. The preferable cleavage of the CPM group may be explained by the polarization of CPM-N17 bond due to a postulation of extreme stability of the cyclopropylcarbinyl cation. 相似文献
9.
El?bieta Hejchman Dorota Maciejewska Irena Wolska 《Monatshefte für Chemie / Chemical Monthly》2008,18(3):1337-1348
The microwave-assisted synthesis of four new 5-acetyl-4,7-dimethoxy-6-hydroxybenzofuran (khellinone) analogs is described.
The structures of the obtained derivatives in the solid state are evaluated on the basis of 13C CP/MAS NMR spectra and theoretical calculations at DFT level. A single crystal X-ray diffraction structure is presented
for 8-acetyl-7-hydroxy-4-methylcoumarin. 1,4-Bis(5-acetyl-4,7-dimethoxybenzofuran-6-yloxy)butane was evaluated for potential
anticancer activity in an in vitro screening panel of 60 human tumor cell lines. Selected leukemia, non-small cell lung cancer, CNS, melanoma, ovarian, and
breast cancer cell lines were sensitive to this compound. 相似文献
10.
Jin ZhangXiao Wang Meipan YangKerou Wan Bing YinYunxia Wang Jianli Li Zhen Shi 《Tetrahedron letters》2011,52(14):1578-1582
A rapid and efficient method for the synthesis of 2-imidazolines and their N-hydroxyethyl derivatives from the reaction of aromatic nitriles with ethylenediamine (EDA) or N-(2-aminoethyl)ethanolamine (AEEA) using cupric indole-3-acetate (Cu(II)-(IAA)2) as a reusable catalyst under reflux and microwave conditions is reported. And seven new N-hydroxyethyl-imidazolines were reported for the first time. 相似文献
11.
Elżbieta Hejchman Dorota Maciejewska Irena Wolska 《Monatshefte für Chemie / Chemical Monthly》2008,139(11):1337-1348
The microwave-assisted synthesis of four new 5-acetyl-4,7-dimethoxy-6-hydroxybenzofuran (khellinone) analogs is described.
The structures of the obtained derivatives in the solid state are evaluated on the basis of 13C CP/MAS NMR spectra and theoretical calculations at DFT level. A single crystal X-ray diffraction structure is presented
for 8-acetyl-7-hydroxy-4-methylcoumarin. 1,4-Bis(5-acetyl-4,7-dimethoxybenzofuran-6-yloxy)butane was evaluated for potential
anticancer activity in an in vitro screening panel of 60 human tumor cell lines. Selected leukemia, non-small cell lung cancer, CNS, melanoma, ovarian, and
breast cancer cell lines were sensitive to this compound.
Correspondence: Elżbieta Hejchman, Department of Organic Chemistry, Faculty of Pharmacy, Medical University of Warsaw, Banacha
1, 02-097 Warsaw, Poland. 相似文献
12.
Behrooz Maleki Shahram Barzegar Zeinalabedin Sepehr Mina Kermanian Reza Tayebee 《Journal of the Iranian Chemical Society》2012,9(5):757-765
A simple, efficient, and environmentally benign route was developed for the preparation of 14-aryl or alkyl-14H-dibenzo[a,j]xanthene, 1,8-dioxo-octahydroxanthene and 12-aryl??8,9,10,12-tetrahydrobenzo[a]xanthene-11-ones from condensation of various aldehydes with (i) ??-naphthol, (ii) cyclic 1,3-dicarbonyl compounds and (iii) ??-naphthol and cyclic 1,3-dicarbonyl compounds, using novel polymeric catalyst [poly(AMPS-co-AA)] under solvent-free conditions. Use of easily available catalyst, shorter reaction times, better yields, simplicity of the reaction, heterogeneous system, and easy work-up are the advantages of the present method. 相似文献
13.
2,4,6-Trichloro-1,3,5-triazine (TCT) efficiently catalyzed the condensation reactions between 1,2-diamines and various enolizable ketones to afford 1,5-benzodiazepines in good to excellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy workup and isolation are notable features of this method. 相似文献
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15.
Silica gel-supported polyphosphoric acid(PPA-SiO2) was found to be an efficient catalyst for the one-pot four-component Hantzsch condensation reaction of aryl aldehydes,dimedone,ethyl acetoacetate and ammonium acetate to afford the corresponding polyhydroquinoline derivatives in high yields.The main advantages of the present approach are short reaction times,clean reaction profiles,simple experimental and workup procedures. 相似文献
16.
Chun-Wei Kuo 《Tetrahedron letters》2006,47(48):8523-8528
Various biologically important 1,5-benzodiazepine derivatives were efficiently synthesized in excellent yields using catalytic amounts of NBS (10 mol %). This inexpensive, nontoxic, and readily available catalyst efficiently catalyzes the condensation of several aromatic as well as aliphatic ketones with substituted o-phenylenediamines. 相似文献
17.
Lijiu Gao Rui Liu Chenxia Yu Changsheng Yao Tuanjie Li Zhaoxin Xiao 《Research on Chemical Intermediates》2014,40(5):2131-2138
2,3-Diaryl quinoxaline derivatives have been efficiently synthesized by cascade, metal-free, and solvent-free reaction of aryl aldehydes with aryl 1,2-diamines initiated by N-heterocyclic carbene. Compared with reported methods, this procedure has the advantages of easy work-up, reduced energy consumption, and elimination of solvent waste, hazards, and toxicity. A group of potentially bioactive compounds has been prepared for biomedical screening. 相似文献
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19.
Prof. Dr. José Luis García Ruano Dr. José Alemán Leyre Marzo Dr. Cuauhtémoc Alvarado Dr. Mariola Tortosa Dr. Sergio Díaz‐Tendero Dr. Alberto Fraile 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(27):8414-8422
We describe the unexpected behavior of the arylsulfonylacetylenes, which suffer an “anti‐Michael” addition of organolithiums producing their alkynylation under very mild conditions. The broad scope, excellent yields, and simplicity of the experimental procedure are the main features of this methodology. A rational explanation of all these results can be achieved by theoretical calculations, which suggest that the association of the organolithiums to the electrophile is a previous step of their intramolecular attack and is responsible for the unexpected “anti‐Michael” reactions observed for substituted sulfonylacetylenes. 相似文献
20.
B. Vigante J. Ozols A. Mishnev G. Duburs B. Chekavichus 《Chemistry of Heterocyclic Compounds》2000,36(7):862-869
Derivatives of 2H-5,6-dihydro-1,3-thiazine are formed by the reaction of acetothioacetic acid ethyl ester with aromatic aldehydes on heating in ethanol in the presence of aqueous ammonia.Latvian Institute of Organic Chemistry, Riga LV-1006, Latvia; e-amil: arcady@osi.lv. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 978–985, July, 2000. 相似文献