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Pachiappa N. Shanmugam Kalv I. Hemanth Kumar Paramasiva N. T. Perumal 《Journal of heterocyclic chemistry》2007,44(4):827-830
A diastereoselective synthesis of 4,5‐dihydrofurans by oxidative addition of 1,3‐dicarbonyl compounds with chalcones mediated by Mn(OAc)3 in moderate to good yields is reported. 相似文献
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Venkatapuram Padmavathi Konda Mahesh Pinnu Thriveni Tippireddy Venkata Ramana Reddy 《Journal of heterocyclic chemistry》2007,44(5):1165-1169
A new class of 1,2,3‐selena/thiadiazoles and 2H‐diazaphospholes were synthesized by exploiting α‐ketomethylene group in phenacylsulfonylacetic acid methyl ester. 相似文献
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Siddheshwar D. Jadhav Nagnnath D. Kokare Sunil D. Jadhav 《Journal of heterocyclic chemistry》2008,45(5):1461-1464
A facile one‐pot synthesis of 2,4,5‐triaryl‐1H‐imidazoles with better yields and shorter reaction time from the condensation of benzil, ammonium acetate and aromatic aldehydes using the catalyst phosphomolybdic acid is described 相似文献
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Zhan‐Hui Zhang Jian‐Jiong Li Yuan‐Zhe Gao Yu‐Heng Liu 《Journal of heterocyclic chemistry》2007,44(6):1509-1512
Iodine was found to be an efficient catalyst for the synthesis of 2‐substituted benzimidazoles by the condensation of orthoesters and 1,2‐phenylenediamines in good to excellent yields under mild reaction conditions. 相似文献
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The reaction of potassium cyanoacetohydroxamate 1 with ethyl 2‐aryl‐hydrazono‐3‐oxobutyrates 2 gave the unexpected pyrazolo[3,4‐c]pyridazines 7 and isoxazolo[5,4‐b]pyridines 10 via a one‐pot reaction. A mechanistic proof is suggested to account for the products. 相似文献
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Hong‐Kui Zhang Wing‐Hong Chan Albert W. M. Leeb Wai‐Yeung Wong 《Journal of heterocyclic chemistry》2008,45(4):957-962
Asymmetric 1,3‐dipolar cycloadditions of chiral nitrones to 1‐propene‐1,3‐sultone ( 1 ) were investigated. Chiral nitrones 6a‐e reacted with sultone 1 in toluene at 90 °C for 24‐36 h to give the corresponding isoxazolidines in moderate yields with high regioselectivities and stereoselectivities. The diastereoselectivity of this reaction varied with the choice of dipolarophile and the steric demands of nitrones. When sultone 1 was allowed to react chiral nitrone 6e , a much better diastereoselectivity of up to 5.1:1 was observed. 相似文献
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Fathi A. Abu‐Shanab A. M. Hessen S. A. S. Mousa 《Journal of heterocyclic chemistry》2007,44(4):787-791
Polysubstituted pyridines 11a,c and 12 were prepared by the reaction of benzoylacetone with dimethylformamide dimethyl acetal followed by treatment with cyanothioacetamide 9a , cyanoacetamide 9b and the anion of malononitrile dimmer 9c in dry DMF. When the reaction was carried out in ethanol as a solvent and piperidine as a base afforded 14a,b . Thienopyridines 16a,b were prepared by the reaction of pyridinethiones 11a and 14a with 2‐chloro‐N‐p‐tolyl‐acetamide ( 15 ). Further reaction of thienopyridines 16a,b with either DMFDMA or nitrous acid to gave 17a,b and 18a,b respectively. The reaction of pyridine derivative 11c with hydrazine and phenylhydrazine afforded the tricyclic compounds 19a,b . 相似文献
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Nicholas A. Jones James W. Antoon Alfred L. Bowie Jr. J. Brian Borak Erland P. Stevens 《Journal of heterocyclic chemistry》2007,44(2):363-367
2,2′‐Bipyridyl‐type compounds may be prepared by Suzuki‐Miyaura coupling of a 2‐pyridylboronic ester with 2‐haloazines and ‐azoles. Ten examples are presented with yields of 47 to 84%. Both arylbromides and arylchlorides undergo the coupling, but the reaction is sensitive to ring substitution adjacent to the halogen. 相似文献