共查询到20条相似文献,搜索用时 15 毫秒
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Kurkutov E. O. Potapov V. A. Musalov M. V. Amosova S. V. 《Russian Journal of General Chemistry》2017,87(2):357-358
The reaction of selenium dihalides with 2-vinyloxyethanol has been performed for the first time, and the method of preparation of bis(1,3-dioxolan-2-ylmethyl)selenide in quantitative yield has been proposed.
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Ikram Chehidi Abaccar Ould Amanetoullah Ahmed Baklouti 《Journal of fluorine chemistry》2010,131(1):66-69
Acid catalysed condensation of F-alkyl α-hydroxy acids with simple aldehydes or ketones gave F-alkyl 1,3-dioxolan-4-ones. When BF3,OEt2 was used as the catalyst, the condensation products were obtained in moderate to good yields and the “cis” isomers are largely favoured, while with HOTs/H2SO4 as catalyst, poor yields and lower stereoselectivities were observed. 相似文献
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The condensation of fluoroacetones with oxalyl fluoride in the presence of potassium fluoride has been shown to yield 2,2-di(fluoroalkyl)-5,5-difluoro-1,3-dioxolan-4-ones. 相似文献
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J. G. Rodriguez N. Martinez-Lopez J. Lopez De Lerma A. Perales 《Journal of heterocyclic chemistry》1989,26(1):135-139
The reduction of the n-(1,3-dioxolan-2-yl)-1-methylpyridinium ions with sodium borohydride has been studied to prepare N-methylformylpiperidines. Deuterium oxide was used as the solvent in order to assign the protons in the nmr spectra. As a product of the reaction, the 4-(1,3-dioxolan-2-yl)-1-methyl-1,2,3,6-tetrahy-dropyridine-borane complex, was isolated and crystallized. A X-ray study of this borane complex has been carried out. 相似文献
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5-HT3 receptor antagonists, such as Ondansetron, are used for anti-emesis after chemotherapy, radiotherapy and operations. Some
Ondansetron analogs possessing piperazine ring as side chains were synthesized in our lab. Thus, one of the two carbonyl groups
of starting material 1,3-cyclohexandione (1) was condensed with phenylhydrazine hydrochloride to form monophenylhydrazone (2). 1,2,3,9-Tetrahydro-4H-carbazol-4-one (3) was prepared from 2
via cyclization and rearranged in the presence of ZnCl2. Through a methylation reaction, compound 3 was converted to 1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one (4). 3-Dimethylaminomethyl substituted compound (5) was synthesized from 4 by a Mannich reaction in glacial acetic acid. Nine novel 1,2,3,9-tetrahydro-9-methyl-3-(4-substituted-piperazin-1-ylmethyl)-4H-carbazol-4-one derivatives (6a–6i) were synthesized through nucleophilic substitution reaction of 5 with piperazines. The structures of all the target compounds were determined by elemental analysis, IR, MS, 1H NMR and 13C NMR spectra. The results of preliminary pharmacological test show that part of the novel compounds have antiemetic activity
comparable to that of the control Ondansetron.
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Translated from Chinese Journal of Organic Chemistry, 2008, 28(2) (in Chinese) 相似文献
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Masoud Sadeghzadeh Fariba Johari Daha Shahab Sheibani Mostafa Erfani 《Journal of Radioanalytical and Nuclear Chemistry》2014,302(3):1119-1125
A mild and simple technique for preparing of 4-benzyl-1-(3-[125I]iodobenzylsulfonyl)piperidine, 4-(3-[125I]iodobenzyl)-1-(benzylsulfonyl)piperazine and their derivatives, as sigma-1 receptor ligands, with relatively high radiochemical yields via nucleophilic substitution reaction by means of isotopic and non-isotopic exchange reactions is described. Some factors affecting the radiochemical yield were commonly studied in presence of acidic medium at elevated temperature. Unfortunately, the radiochemical yields were weak. Some attempts were carried out in presence of polar aprotic solvents to enhance the radiochemical yield. N,N-Dimethylformamide was proved highly efficient for preparing of radioiodinated 4-benzyl-1-(3-iodobenzylsulfonyl)piperidine (4-B-[125I]-IBSP, 70 ± 5.7 %) and 4-(3-iodobenzyl)-1-(benzylsulfonyl)piperazine (4-[125I]-IBBSPz, 72 ± 6.0 %) at moderate temperature (100–105 °C) within 8 h. The specific activities of 4-B-[125I]-IBSP and 4-[125I]-IBBSPz (6,534.2 and 5,927.4 MBq/mmol) were obtained respectively. 相似文献
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Guan-Yeow Yeap Wan-Sinn Yam Masato M. Ito Yumika Takahashi Yoshiyuki Nakamura Wan Ahmad Kamil Mahmood Peng-Lim Boey Shafida Abd Hamid Ewa Gorecka 《Liquid crystals》2007,34(5):649-654
A new homologous series of 7-acyloxy-3-(4-acyloxyphenyl)-4H-1-benzopyran-4-ones was synthesized and characterized by elemental analysis and spectroscopic techniques along with thermal behaviour study using differential scanning calorimetry. Texture observation was performed under the polarizing optical microscope from which the derivatives were found to exhibit different molecular organizations as exemplified by various mesophases. Whilst the compounds containing butanoyloxy and hexanoyloxy groups behave as nematogens, the other compounds with heptanoyloxy and longer side chains show a SmC phase. The octadecanoyloxy derivative was the only member showing a monotropic SmC phase. The difference in phase behaviour is discussed based on the molecular structure and the presence of a lateral dipole which can be associated with the intermolecular interaction within the mesophase. 相似文献
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以L-抗坏血酸(1)为原料,经3步反应制得(S)-缩异丙氧叉甘油醛(4).该手性醛与苄胺缩合制得相应的手性亚胺(5).甘氨酸经保护后制成酰氯,在有机碱作用下首先生成不稳定的烯酮(8),继与手性亚胺5迅速进行[2+2]环加成反应,合成标题化合物N-苄基-3(S)-邻苯二甲酰亚胺基-4(S)-[4(S)-2,2-二甲基-1,3-二氧环戊-4-基]-2-氧吖丁啶.由于环加成的面向立体选择性容易控制,由此所得产物的光学纯度和化学收率均较高 相似文献
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K. A. Volkova A. N. Nikol'skaya E. P. Levanova A. N. Volkov B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1979,15(12):1296-1298
Alkylthio-substituted dienic 1,3-dioxolan-2-ones and bis(4,4-diorganyl-5-methyli-dene-1,3-dioxolan-2-ones) were obtained in high yields by the reaction of 2-methyl-6-alkylthio-5-hexen-3-yn-2-ols and tertiary diacetylenic glycols with carbon dioxide under pressure in the presence of catalytic amounts of triethylamine and monovalent copper salts.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1617–1619, December, 1979.Original article submitted January 24, 1979. 相似文献
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Ketalization of benzophenones with epichlorohydrin or 3-chloropropane-1,2-diol gave 2,2-diaryl-4-chloromethyl-1,3-dioxolanes,
which were used to alkylate sodium salts of imid-azole or 1,2,4-triazole. The resulting 1-[(2,2-diaryl-1,3-dioxolan-4-yl)methyl]-1H-azoles exhibit high fungicidal activities.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 940–944, May, 2007. 相似文献
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Reactions of 3-methyl-6-[4-(4-hydroxyphenyl)-1-piperazinyl]-2(3H)-benzoxazolone, 3-methyl-6-[4-(4-hydroxy-phenyl)-1-piperazinyl]-2(3H)-benzothiazolone and 1,3-dimethyl-5-[4-(4-hydroxyphenyl)-1-piperazinyl]-2(3H)-benzimidazolone with cis-{[2-(2,4-dichlorophenyl) -2-(1H-imidazol-1-ylmethyl)]-1,3-dioxolan-4-yl}methyl meth-anesulfonate in the presence of sodium hydride furnish the title compounds. 相似文献
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Golubyatnikova L. G. Anpilogova G. R. Khisamutdinov R. A. Murinov Yu. I. 《Russian Journal of General Chemistry》2012,82(2):310-316
Extraction of hydrochloric and nitric acid with 1-{[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl]-methyl}-1H-1,2,4-triazole (propiconazole) and hydrochloric acid with (RS)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-yl-methyl)-pentan-3-ol (tebuconazole) was studied. It is established that extraction of acids proceeds with the formation of monosolvates as an exothermic process. Effective extraction constants of acids are evaluated. By means of the IR and 1H NMR spectroscopy it was shown that the protonaccepting center of tebuconazole is N4 atom of the triazole ring. 相似文献