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Pure Appl. Chem., 1994, Vol. 66, No. 4, pp. 759-764

http://dx.doi.org/10.1351/pac199466040759

Models of biological systems and biological processes

U. K. Pandit

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  • Zinczuk Juan, Ledesma Ana Estela, Brand��n Silvia Antonia, Piro Oscar Enrique, L��pez-Gonz��lez Juan Jes��s, Ben Altabef A��da: Structural and vibrational study of 2-(2���- furyl)-4,5-1H-dihydroimidazole. J Phys Org Chem 2009, 22, 1166. <http://dx.doi.org/10.1002/poc.1572>
  • Caterina M. Cristina, Perillo Isabel A., Boiani Lucía, Pezaroglo Horacio, Cerecetto Hugo, González Mercedes, Salerno Alejandra: Imidazolidines as new anti-Trypanosoma cruzi agents: Biological evaluation and structure–activity relationships. biorg med chem 2008, 16, 2226. <http://dx.doi.org/10.1016/j.bmc.2007.11.077>
  • Clemens Nicole, Sereda Oksana, Wilhelm Ren?: Unexpected behaviour of tosylated and acetylated imidazolinium salts. Org Biomol Chem 2006, 4, 2285. <http://dx.doi.org/10.1039/b601104g>
  • Hao Junsheng, Deng Bing, Guo Wei, Huo Fangjun, Zhang Yongbin, Xia Chizhong, Li Donghong: A Convenient Synthesis of 1‐Tosyl‐3, 4‐Dimethyl Imidazolium Salt and N,N,N′‐Trisubstituted Ethylendiamine Derivatives. Synth Common 2004, 34, 3535. <http://dx.doi.org/10.1081/SCC-200030990>
  • Kang Congmin, Feng Dacheng, Qi Chuansong, Zhao Weian, Cai Zhengting: Comparative study of folate cofactor models. Int J Quantum Chem 2002, 87, 152. <http://dx.doi.org/10.1002/qua.10083>
  • Xia Chizhong, Wang Hongxing, Zhao Bingjun, Chen Jianxin, Kang Congmin, Ni Yanping, Zhou Peiwen: A CONVENIENT SYNTHESIS OF IMIDAZOLIUM SALTS AND TRISUBSTITUTED ETHYLENEDIAMINE DERIVATIVES. Synth Common 2002, 32, 1447. <http://dx.doi.org/10.1081/SCC-120003643>
  • Xia Chizhong, Hao Junsheng, Tang Yiqing, Ni Yanping, Zhou Peiwen: REACTIONS OF 2,3-DIARYL-1-METHYL-4,5-DIHYDROIMIDAZOLIUM IODIDES WITH NUCLEOPHILIC REAGENTS. Synth Common 2002, 32, 1457. <http://dx.doi.org/10.1081/SCC-120003644>
  • Xia Chizhong, Chen Jianxin, Wang Hongxing, Kang Congmin, Zhao Bingjun, Ni Yanping, Zhou Peiwen: NUCLEOPHILIC ADDITION TO 1,2-DIMETHYL-3-ARYLSULFONYL- 4,5-DIHYDROIMIDAZOLIUM IODIDES. Synth Common 2002, 32, 2979. <http://dx.doi.org/10.1081/SCC-120012987>
  • Singh Kamaljit, Deb Prasant K, Venugopalan P: Modified Pictet–Spengler reaction. A highly diastereoselective approach to 1,2,3-trisubstituted-1,2,3,4-tetrahydro-β-carbolines using perhydro-1,3-heterocycles. Tetrahedron 2001, 57, 7939. <http://dx.doi.org/10.1016/S0040-4020(01)00763-3>
  • Xia Chizhong, Tang Yiqing, Zhou Peiwen: Nucleophilic addition to 3-methyl-1-(4-nitrophenyl)-2-phenyl-4,5-dihydroimidazolium iodide. J Heterocyclic Chem 2000, 37, 1329. <http://dx.doi.org/10.1002/jhet.5570370552>
  • Jones Raymond C.F., Dimopoulos Paschalis: A New Protocol for the Synthesis of N(1)-Unsubstituted 2-Substituted 2-Imidazolines. Tetrahedron 2000, 56, 2061. <http://dx.doi.org/10.1016/S0040-4020(00)00108-3>
  • Xia Chizhong, Kang Congmin, Zhao Bingjun, Chen Jianxin, Wang Hongxing, Zhou Peiwen: A Convenient Synthesis of N, N, N'-Trisubstituted Ethylenediamine Derivatives From 2-Methyl-2-imidazoline. Synth Common 2000, 30, 3307. <http://dx.doi.org/10.1080/00397910008086970>
  • Igarashi Mamoru, Kambe Tohru, Tada Masaru: Syntheses of folic acid models, 6-(N-acylarylamino)methyllumazines. J Heterocyclic Chem 1996, 33, 341. <http://dx.doi.org/10.1002/jhet.5570330222>