共查询到20条相似文献,搜索用时 140 毫秒
1.
A. Kakanejadifard L. Mahmodi A. Yari A. Mohajeri 《Journal of heterocyclic chemistry》2006,43(6):1695-1697
3,7‐Di(3‐nitrophenyl)‐1,5‐dioxa‐3,7‐diazacyclooctane was prepared from 3‐nitroaniline and formaldehyde in acetonitrile. Conformational behavior of ring inversion of the molecule was studied so it prefers a crown conformation. The evaluated ΔG* was approximately 58.0 ± 1.0 kJ/mole. The X‐ray structure determination of the compound shows a crown conformation, in line with two‐anomeric effect in N‐C‐O moiety. 相似文献
2.
Sivaperuman Saravanan Arumugam Nithya Shanmugam Muthusubramanian 《Journal of heterocyclic chemistry》2006,43(1):149-155
The synthesis of a new set of selenadiazoles, 4‐aryl‐5‐(1‐aryl‐2‐methyl‐2‐nitropropyl)‐1,2,3‐selenadiazoles ( 4 ) derived from 2‐[4‐methyl‐4‐nitro‐1,3‐diarylpentylidene]‐1‐hydrazinecarboxamide ( 3 ) has been reported. THF has been found to be the solvent of choice for this reaction. Structural features of 3 and 4 have been analyzed by NMR and X‐ray techniques. 相似文献
3.
Shujiang Tu Jinpeng Zhang Xiaotong Zhu Yan Zhang Qian Wang Jianing Xu Bo Jiang Runhong Jia Junyong Zhang Feng Shi 《Journal of heterocyclic chemistry》2006,43(4):985-988
Four‐component cyclocondensation of aromatic aldehydes, malononitrile, dimedone and ammonium acetate proceeds under microwave irradiation in solvent free conditions to give highly functionalized hexahydroquinolines in excellent yields. 相似文献
4.
Bobby N. Brewer Keith T. Mead Charles U. Pittman Kaitao Lu Peter C. Zhu 《Journal of heterocyclic chemistry》2006,43(2):361-363
The oxidation of ortho‐phthalaldehyde to phthalic acid in aqueous solutions can be remedied by the addition of various cyclic acetals, which, when reacted with phthalic acid, yields ortho‐phthalaldehyde, thus prolonging the lifetime of the ortho‐phthalaldehyde disinfection solution. 相似文献
5.
Xinglong Jiang Guang‐Pei Chen Kapa Prasad Oljan Repi
Thomas J. Blacklock 《Journal of heterocyclic chemistry》2006,43(6):1725-1728
A general method for the synthesis of 8‐hydroxy‐6‐substituted‐1,7‐naphthyridines is described using acylation of the dianion derived from tert‐butylamide 1 , followed by cyclization of the resulting intermediate ketones 2 with ammonium acetate. 相似文献
6.
Síria A. Barros M. Sameiro T. Gonçalves Ana M. F. Oliveira‐Campos Fernanda R. P. Proença 《Journal of heterocyclic chemistry》2007,44(1):13-19
A simple and efficient method was developped for the synthesis of 3‐(5‐amino‐4‐cyano‐1H‐imidazol‐1‐yl)‐4‐substituted benzoic acids 3 . These compounds were isolated by intramolecular cyclisation of the corresponding 3‐{[(Z)‐2‐amino‐1,2‐dicyano‐vinyl]amino}methyleneaminobenzoic acids in the presence of base. 相似文献
7.
I. Philipova G. Dobrikov K. Krumova J. Kaneti 《Journal of heterocyclic chemistry》2006,43(4):1057-1063
A series of 2‐substituted‐4(3H)‐quinazolinones 13‐20 has been synthesized in good yields using the reaction of double lithiated 2‐methylquinazolinone‐4 with a variety of aromatic aldehydes. They have been easily transformed in high yields into the corresponding 2‐substituted conjugated derivatives 21‐28 bearing terminal aryl groups by F3CCOOH mediated dehydration. 相似文献
8.
A. K. El‐Shafie A. M. Soliman A. A. Sultan E. Abd‐Alla 《Journal of heterocyclic chemistry》2006,43(1):133-137
2(1‐Acetyl‐2‐oxopropylidene)naphtho[2,3‐d][1,3]dithiole‐4,9‐dione 1 reacts with a variety of bidentates reagents to give some new functionally substituted spiro naphthodithiole‐4,9‐dione derivatives. 相似文献
9.
Zhang‐Gao Le Jian‐Ping Xu Huo‐Yu Rao Min Ying 《Journal of heterocyclic chemistry》2006,43(4):1123-1124
The one‐pot direct synthesis of 2‐aminobenzothiazoles from phenyl isothiocyanate and amines using a new reagent of 1‐butyl‐3‐methylimidazolium tribromide ([Bmim]Br3) in ionic liquid 1‐butyl‐3‐methylimidazolium tetraflouoroborate ([Bmim]BF4) is described. 相似文献
10.
Giuseppe Granata Salvatore Barbagallo Antonio Perdicaro Agostino Marrazzo Andrea Santagati Laura Lombardo Venera Cardile 《Journal of heterocyclic chemistry》2006,43(4):1099-1104
Methane sulfonamide derivatives of 3‐amino‐2‐thioxo‐2,3‐dihydrothieno[2,3‐d]pyimidin‐4(1H)‐one, potential selective COX‐2 inhibitors, were synthesized and their structural elucidation is here reported. Some derivatives, at 10 μM concentration, showed a significant percentage of inhibition in some in vitro experiments. 相似文献
11.
Tricyclic dihydropyridines like ZM244085 are potential KATP channel openers. In this study 3‐cyanophenyl ring of ZM244085 was replaced with imidazolyl ring. So, 9‐[1‐benzyl‐5‐(alkylsulfonyl)‐1H‐2‐imidazolyl]perhydro‐1,8‐acridinediones ( 5d‐f ) were synthesized from 2‐alkylsulfonyl‐1‐benzyl‐5‐formylimidazole ( 4d‐f ) and cyclohexane‐1,3‐dione according to classical Hantzch synthesis as potential potassium channel modulators. 相似文献
12.
Romualdas Smičius Milda Malvina Burbuliene Virginija Jakubkienė Emilija Udrwėnaitė Povilas Vainilavičius 《Journal of heterocyclic chemistry》2007,44(2):279-284
Various 4‐amino‐2,3‐dihydro‐4H‐triazoles with aromatic, aliphatic and heterocyclic substituents at the C(5) position were synthesized from corresponding esters and thiocarbohydrazide. This method allows the synthesis these heterocycles in a short time and at reduced expenses. 相似文献
13.
Vinodkumar Ramanatham Murugulla Adharvana Chari Pramod Kumar Dubey 《Journal of heterocyclic chemistry》2007,44(6):1537-1541
An alternate method for the convenient preparation of the imidazo[4,5‐b]pyridines from 2,3‐pyridinediamine and 2‐aryl‐3(1)‐benzoxazine‐4H‐one has been illustrated. The mechanistic pathway for the formation of the product 4 has been proposed. All the compounds prepared herein were screened for their anti‐ bacterial properties. 相似文献
14.
(Un)substituted benzaldehyde (5‐aryl‐1,3,4‐thiadiazol‐2‐yl)hydrazones were efficiently synthesized by reactions of (un)substituted benzaldehyde thiocarbohydrazones with aromatic carboxylic acids by using silica‐supported dichlorophosphate as a recoverable dehydrant under microwave irradiation. The protocol has advantages of short reaction time, high yield, easy work‐up procedure and no environmental pollution. 相似文献
15.
Avijit Banerji Pizush Kanti Biswas Debasish Bandyopadhyay Maya Gupta Thierry Prangé Alain Neuman 《Journal of heterocyclic chemistry》2007,44(1):137-143
Investigation of cycloadditions of C‐aryl‐N‐(4‐chlorophenyl)nitrones to N‐cinnamoyl piperidines was carried out. Two diastereoisomeric and one regioisomeric cycloadducts, and in some cases ring‐opened compounds were characterized by spectroscopic and X‐ray data. Molecular modelling was carried out for conformational studies. 相似文献
16.
Khodabakhsh Niknam Seyed Mehdi Razavian Mohammah Ali Zolfigol Iraj Mohammahpoor‐Baltork 《Journal of heterocyclic chemistry》2006,43(1):199-202
A combination of methanesulfonic acid and sodium nitrite in the presence of wet SiO2 was used as an effective oxidizing agent for the oxidation of 1,4‐dihydropyridines to the corresponding pyridine derivatives under mild and heterogeneous conditions in excellent yields. 相似文献
17.
Malek Taher Maghsoodlou Sayyed Mostafa Habibi Khorassani Lotfali Saghatforoush Farhad Maghfuri Ghasem Marandi Roya Kabiri 《Journal of heterocyclic chemistry》2008,45(1):289-293
High hindrance Hexa tert‐butoxy carbonyl dipyrrolophenanthroline and helical dihydropyrrolophen‐anthroline compounds were prepared from reactions between di tert‐butyl acetylenedicarboxylate and 1,10‐phenanthroline in polar solvents media. 相似文献
18.
Karel D. Klika Kalevi Pihlaja Jn Imrich Mria Vilkov Juraj Bernt 《Journal of heterocyclic chemistry》2006,43(3):739-743
N‐Acridin‐9‐yl methyl N′‐acridin‐9‐yl thiourea spontaneously spiro cyclises via nucleophilic attack of the methylene carbon onto the C‐9 of the other acridine moiety. The thiourea, upon reaction with bromoacetonitrile, provided a spiro fused‐bicyclic product displaying unusual dynamic behavior. 相似文献
19.
Malose J. Mphahlele Mutshinyalo S. Nwamadi Peace Mabeta 《Journal of heterocyclic chemistry》2006,43(2):255-260
The C‐3 brominated and iodinated derivatives were prepared from the corresponding 2‐arylquinolin‐4(1H)‐ones and their NMe‐4‐oxo derivatives using pyridinium tribromide in acetic acid or iodine‐Na2CO3 mixture in THF. The results of further studies of chemical transformation of the prepared α‐haloenones and preliminary antitumour activity of the 3‐bromo NH‐4‐oxo and NMe‐4‐oxo derivatives are also described. 相似文献
20.
Ganesabaskaran Sivaprasad Radhakrishnan Sridhar Paramasivan T. Perumal 《Journal of heterocyclic chemistry》2006,43(2):389-394
A selective and easy method is described for the synthesis of 4,5‐dihydro‐2H‐benzo[g]indazoles and 8,9‐dihydro‐2H‐benzo[e]indazoles by the Vilsmeier‐Haack reaction of various tetralone phenylhydrazones under thermal and microwave irradiation conditions. 相似文献