期刊文献+

1,2,3,4-四氢喹啉衍生物合成进展 被引量:3

Progress in the Synthesis of 1,2,3,4-Tetrahydroquinoline Derivatives
原文传递
导出
摘要 1,2,3,4-四氢喹啉类化合物是一类重要的含氮杂环化合物,具有众多的生物活性和广泛的用途,因此,四氢喹啉合成新方法的研究受到人们的关注。本文分别从通过氢化还原策略、关环转化反应策略以及通过多分子缩合反应策略等几个方面综述1,2,3,4-四氢喹啉衍生物合成的进展。 1,2,3,4-Tetrahydroquinolines are a class of important nitrogen-containing heterocyclic compounds and exhibit numerous biologic activities and extensive applicant values, hence seeking their new synthetic methods have been paid more attention. The progress in the synthesis of 1,2,3,4-tetrahydroquinoline derivatives from hydrogenation reduction, cyclization and transform, and multi-molecule condensation approaches were introduced in this paper.
作者 蔡小华 谢兵
出处 《化学通报》 CAS CSCD 北大核心 2012年第5期407-413,共7页 Chemistry
基金 国家自然科学基金项目(20962006) 贵州省科技基金项目(LKM[2011]26)资助
关键词 1 2 3 4-四氢喹啉 氢化还原 关环转化 多分子缩合 1,2,3,4-Tetrahydroquinolines, Hydrogenation reduction, Cyclization and transform, Multi-molecule condensation
  • 相关文献

参考文献38

  • 1J H Rakotoson, N Fabre, I Jacquemond-Collet et al. Planta Med. , 1998,64 (8) :762 - 763.
  • 2I Jacquemond-Collet,F Benoit-Vical,A Valentin et al. Planta Med. ,2002,68( 1 ) :68 - 69.
  • 3H Nakayama,M E Ferreira,A R de Arias et al. Phytother. Res. ,2001,15(7) :630 -632.
  • 4I Jacquemond-Collet, S Hannedouche, N Fabre et al. Phytochem. , 1999,51 ( 3 ) : 1167 - 1169.
  • 5R K Chen,X C Yang,H N Tian et al. Chem. Mater. , 2007,19(16) :4007 -4015.
  • 6吴伟兵,王明亮,黄维,孙岳明,崔一平,徐春祥.1,2,3,4-四氢喹啉-4-酮衍生物的线性及非线性光学性质[J].化学学报,2008,66(14):1700-1706. 被引量:4
  • 7T Malinauskas, J Stumbraite, V Getautis et al. Dyes and Pigments,2009,81 ( 2 ) : 131 - 136.
  • 8T A Rano,E S McMaste,P D Pehon et al. Bioorg. Med. Chem. Lett. ,2009,19(9) :2456 -2460.
  • 9O B Wallace, K S Lauwers, S A Jones et al. Bioorg. M ed. Chem. Lett. ,2003,13 ( 11 ) : 1907 - 1910.
  • 10C Parmenon, J Guillard, D H Caignard et al. Bioorg. Med. Chem. Lett. ,2009,19 (10) :2683 -2687.

二级参考文献34

  • 1钱鹰,林保平,孙岳明,王刚,崔一平,袁春伟.AπDπA型咔唑衍生物三阶光学非线性的Z-扫描研究[J].化学学报,2005,63(23):2141-2146. 被引量:2
  • 2钱鹰,路志锋,吕昌贵,宋坤忠,崔一平,孙岳明,林保平.1,3,4-噁二唑衍生物的双光子吸收和双光子泵浦荧光[J].化学学报,2006,64(24):2473-2478. 被引量:2
  • 3Kim, O. K.; Lee, K. S.; Woo, H. Y.; Kim, K. S.; He, G. S.; Swiatkiewicz, J.; Prasas, P. N. Chem. Mater. 2000, 12, 284.
  • 4Ventelon, L.; Charier, S.; Moreaux, L.; Mertz, J. Angew. Chem., Int. Ed. Engl. 2001, 40, 2098.
  • 5Bagatolli, L. A.; Gratton, E. J. Fluoresc. 2001, 11,141.
  • 6Albota, M.; Beljonne, D.; Brdas, J. L.; Ehdich, J. E.; Fu, J. Y.; Heikal, A. A.; Hess, S. E.; Kogej, T.; Levin, M. D.; Marder, S. R.; McCord-Maughon, D.; Perry, J. W.; Rckel, H.; Rural, M.; Subramaniam, G.; Webb, W. W.; Wu, X. L.; Xu, C. Science 1998, 281, 1653.
  • 7Abbotto, A.; Beverina, L.; Bozio, R.; Bradamante, S.; Ferrante, C.; Pagani, G. A.; Signorini, R. Adv. Mater. 201111, 12, 1963.
  • 8Kim, O. K.; Lee, K. S.; Woo, H. Y.; Kim, K. S.; He, G. S.; Swiatkiewicz, J.; Prasad, P. N. Chem. Mater. 2000, 12, 284.
  • 9He, G. S.; Przemyslaw, P. M.; Tzu-Chau, L.; Prasad, P. N. Nature 2002, 415, 767.
  • 10Fu, J.; Przhonska, O. V.; Padilha, L. A.; Hagan, D. J.; Van Stryland, E. W. Chem. Phys. 2006, 321,257.

共引文献3

同被引文献24

  • 1刘晓辉,刘伟,周勇亮,王今堆,马林,黄仲立,李铁津.酚类聚合物在水相胶束中的酶促合成[J].功能高分子学报,1995,8(3):308-314. 被引量:7
  • 2许海燕,徐梁华,庞正智.过氧化物酶催化酚聚合的研究[J].功能高分子学报,1995,8(3):355-359. 被引量:9
  • 3V Sridharan, P A Suryavanshi, J C Men6ndez. Advancesin the Chemistry of Tetrahydroquinolines [ J ] . ChemicalReviews, 2011, 111(11); 7 157 ?7 259.
  • 4E Reimann, H Unger. Selektive katalytische Hydrierungenund Hydrogenolysen, 2. Mitt. 1) Einfache Darstellung von4 - Methyl -5 ,6,7,8 - tetrahydrochinolin[ J]. Archiv derPharmazie, 1983,316(3): 210-212.
  • 5AM Maj,I Suisse, C M^liet. , et al. Highly enantioselec-tive hydrogenation of new 2 - functionalized quinoline de-rivatives [J]. Tetrahedron Letters, 2012,53(35) : 4 747-4 750.
  • 6F Fache. Solvent Dependent Regioselective Hydrogenationof Substituted Quinolines[ J]. Synlett,2004,2004( 15 ):2 827 -2 829.
  • 7T E D"Ambra, K G Estep, M R Bell. , et al. Conforma-tionally Restrained Analogs of Pravadoline: Nanomolar Po-tent, Enantioselective, ( Aminoalkyl) indole Agonists of theCannabinoid Receptor [ J] . Journal of Medicinal Chemis-try, 1992,35(1): 124 ?135.
  • 8A R Katritzky,S Rachwal,B Rachwal. Recent progress inthe synthesis of 1,2,3 ?4, - tetrahydroquinolines[ J]. Tet-rahedron, 1996, 52(48) :15 031 - 15 070.
  • 9G W Gobble, P W Heald. Reactions of Sodium Boro-hydride in Acidic Media; III. Reduction and Alkylation ofQuinoline and Isoquinoline with Carboxylic Acids [ J ].Synthesis, 1975,1975(10): 650-652.
  • 10A Nose, T Kudo. Studies of Reduction with the Sodium, Borohydride - Transition Metal Boride System. I : Reduc-tion of Nitro and the Other Functional Groups with the So-dium Borohydride - Nickel Boride System[ J]. Chemicaland Pharmaceutical Bulletin, 1988,36(4) : 1 529 ?1533.

引证文献3

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部