计算机文献检索报告

外文文献检索报告检索关键词：the Triazene Reagents检索过程：打开校园网，点击“图书馆电子资源”，进入界面后点击“外文电子资源”，并进入“Elsevier Science 电子期刊”，点击“Search”，并在其中输入“the Triazene Reagents”，检索后即可得到大约15页有关氮烯化合物的研究论文，从中选取几篇论文列举如下，检索结果：【1】Synthesis of a new triazene reagent and its application for the determination of silver(I) by the Rayleigh light-scattering ；Analytica Chimica Acta；Received 6 August 1998; accepted 10December 1998，page,45-50;Yunkun Zhaoa, Qiu-E Caoa, Zhide Hua, Qiheng XubISSN: 0003-2670【2】The synthesis and application of1-(o-nitrophenyl)-3-(2-thiazolyl)triazene for the determination of palladium(II) by the resonance enhanced Rayleighlight-scattering technique；Spectrochimica Acta Part A； Molecular and Biomolecular Spectroscopy；Received 29 June 1999; accepted 30 September 1999；page45-50; Yunkun Zhaoa, Qiu-E Caoa, Zhide Hua, Qiheng XubISSN: 1386-1425【3】A facile route to the new triazene dyes based on substituted pyrazolidin-3,5-dione derivatives；Dyes and Pigments；Received 14 April 2011 Received in revised form 28 July 2011 Accepted 29 July 2011 Available online 9 August 2011；page45-50,Jalal Isaad，Fouad Malek, Ahmida El Achari；ISSN: 0143-7208【4】Novel platinum(II) selective membrane electrode based on 1,3-bis(2-cyanobenzene)triazene；Talanta；Received 29 October 2008 Received in revised form December 2008 Accepted 30 December 2008 Available online 22 January 2009；page121-125,Mohammad BagherGholivand, Moslem Mohammadi,Mehdi Khodadadian, Mohammad KazemRofouei；ISSN: 0039-9140【4】Mercury(II) selective membrane electrode based on1,3-bis(2-methoxybenzene)triazene；Materials Science andEngineering: C；Received 10 February 2009 Received in revised form18 April 2009 Accepted 27 April 2009 Available online 5 May 2009；page87-92,Mohammad Kazem Rofouei , Moslem Mohammadi , Mohammad Bagher Gholivand；ISSN: 0928-4931【5】Structural and solution studies of a novel tetranuclear silver(I) cluster of [1,3-di(2-methoxy)benzene]triazene；Inorganica ChimicaActa；Received 19 May 2006; received in revised form 17 September 2006; accepted 20 September 2006，Available online 29 September 2006；page2015-2019,Mahmood Payehghadr, Mohammad Kazem Rofouei, Ali Morsali Mojtaba Shamsipur；ISSN: 0020-1693二次检索：下面进行二次检索，在检索结果的左上方对文章进行筛选，在“Content Type”中选择“Journal”,在“Journal”中选择“Tetrahedron”，在“Year”中选择“2012(13)”，点击“Limit to”,检索得到一篇符合要求的文献，列举如下：Synthesis of 1,3,5-trisubstituted-1,2,4-triazoles bymicrowave-assisted N-acylation of amide derivatives and theconsecutive reaction with hydrazine hydrochlorides；Tetrahedron；Received 30 December 2011 Accepted 4 January 2012 Available online8 January 2012；page2045-2051; Jongbok Lee, Myengchan Hong, YoonchulJung, Eun Jin Cho , Hakjune Rhee;ISSN: 0040-4020对文章内容分析如下：Background:1,2,4-Triazole analogues have been attracting attentionover the last decade due to their biological activities, such as antiviral, antitumor, and anti-inflammatory activities.1e3 1,2,4-Triazoles can be prepared by the reaction of hydrazonyl chlorides with aromatic or aliphatic nitriles in the presence of AlCl3 or Yb(OTf)3.4,5 Its synthesis can also be accomplished by cyclization of 1,2,4-triazene from hydrazonyl chlorides with a primary amine in the presence of triethylamine followed by oxidation using various oxidizing agents, such as Ag2CO3, NaOCl, Ca(OCl)2, DesseMartin periodinane, Ley’s TPAP/NMO, and H2O2/KOH.These methods, however, have limited functional group tolerance and require more than stoichiometric amounts of reagents. Thus it is desirable to develop more efficient and general method for the preparation of 1,3,5- trisubstituted-1,2,4-triazoles under mild reaction conditions. Over recent years, a great number of publications have reported.Study significance: Facile and efficient procedures for theN-acylation reaction of amide derivatives with various acid anhydrides and the cyclization reaction of N-acylated amide derivatives with various hydrazine hydrochlorides were described. The reactions were carried out under microwave irradiation to give products in good yields in a few minutes. The synthesis of 1,3,5-trisubstituted-1,2,4-triazoles from benzamides can also be accomplished in a simple one-pot sequential reaction.Research institution： Department of Bionanotechnology, HanyangUniversity, Sa 3-Dong 1271, Ansan, Kyunggi-Do 426-791, Republic of Korea Department of Chemistry and Applied Chemistry, Hanyang University, Sa 3-Dong 1271, Ansan, Kyunggi-Do 426-791, Republic of Korea.References and notes:【1】. Al-Soud, Y. A.; Al-Dweri, M. N.; Al-Masoudi, N. A. Farmaco 2004, 59, 775.【2】. Demirbas, N.; Ugurluoglu, R.; Demirbas, A. Bioorg. Med. Chem. 2002, 10, 3717.【3】. Tozkoparan, B.; Gokhan, N.; Aktay, G.; Yesilada, E.; Ertan, M. Eur. J. Med. Chem.2000, 35, 743.【4】. Conde, S.; Corral, C.; Madronero, R. Synthesis 1974, 28. 【5】. Su, W.; Yang, D.; Li, J. Synth. Commun. 2005, 35, 1435. 【6】. Paulvannan, K.; Chen, T.; Hale, R. Tetrahedron 2000, 56, 8071. 【7】. Paulvannan, K.; Hale, R.; Sedehi, D.; Chen, T. Tetrahedron 2001, 57, 9677.【8】. Buzykin, B. I.; Bredikhina, Z. A. Synthesis 1993, 59.【9】. Caddik, S. Tetrahedron 1995, 51, 10403.【10】. Lidstrom, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225.【11】. Jagerovic, N.; Hernandez-Folgado, L.; Alkorta, I.; Goya, P.; Navarro, M.; Serrano,A.; Fonseca, F. R.; Dannert, M. T.; Alsasua, A.; Suardiaz, M.; Pascual, D.; Martin,M. I. J. Med. Chem. 2004, 47, 2939. 【12】. Czollner, L.; Szilagyi, G.; Lango, J.; Janaky, J. Arch. Pharm. 1990, 323, 225.【13】. Yoon, U. C.; Cho, S. J.; Lee, Y. J.; Mancheno, M. J.; Mariano, P. S. J. Org. Chem. 1995,60, 2353.。