期刊文献+

吲哚与硝基烯的Friedel-Crafts反应的研究进展 被引量:6

Research Progress in Friedel-Crafts Reaction of Indoles and Nitroalkenes
原文传递
导出
摘要 吲哚作为核心结构广泛存在于生物碱和药物中,吲哚衍生物在生物体的生理活动中起着重要的作用,其中吲哚和硝基烯的Friedel-Crafts是生成吲哚衍生物的重要方法.按照反应中催化剂种类的不同分为:(1)无催化剂,(2)离子液体催化剂,(3)金属盐催化剂,(4)配合物催化剂,(5)Br nsted酸催化剂,(6)有机小分子催化剂,(7)其他类型催化剂.对吲哚与硝基烯的Friedel-Crafts反应的情况进行了综述. Indoles, as the core structure, exist widely in many alkaloid natural products and pharmaceuticals. The derivatives of indole play an important role in organism physiological activities. The Friedel-Crafts reaction of indoles and nitroalkenes is an important method to generate indole derivatives. According to the kinds of the catalyst in the reaction, the Friedel-Crafts reactions of indoles and nitroalkenes were summarized in this paper as follows: (1) catalyst-free, (2) ionic liquid catalyst, (3) metal salt catalyst, (4) coordination compound catalyst, (5) Br?nsted acid catalyst, (6) small molecular organic catalyst, (7) other catalysts.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2013年第9期1919-1931,共13页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(Nos.21262034 20962018 20862015 20562011)资助项目~~
关键词 FRIEDEL-CRAFTS反应 吲哚 硝基烯 催化剂 Friedel-Crafts reaction indole nitroolefin catalyst
  • 相关文献

参考文献2

二级参考文献62

  • 1Poulsen,T.B.;Jorgensen,K.A.Chem.Rev.2008,108,2903.
  • 2Bigi,F.;Casiraghi,G.;Casnati,G.;Sartori,G.;Fava,G.G.;Belicchi,M.F.J.Org.Chem.1985,50,5018.
  • 3Herrera,R.P.;Sgarzani,V.;Bernardi,L.;Ricci,A.Angew.Chem.,Int.Ed.2005,44,6576.
  • 4Zheng,C.;Sheng,Y.F.;Li,Y.X.;You,S.L.Tetrahedron 2010,66,2875.
  • 5Olah,G.A.;Khrisnamurti,R.;Prakash,G.K.S.In ComprehensiveOrganic Synthesis,Vol.3,Pergamon,New York,1991,pp.293~339.
  • 6Sheng,Y.F.;Gu,Q.;Zhang,A.J.;You,S.L.J.Org.Chem.2009,74,6899.
  • 7Itoh,J.;Fuchibe,K.;Akiyama,T.Angew.Chem.,Int.Ed.2008,47,4016.
  • 8Bandini,M.;Melloni,A.;Umani-Ronchi,A.Angew.Chem.,Int.Ed.2004,43,550.
  • 9Bolm,C.;Hildebrand,J.P.;Muniz,K.;Hermanns,N.Angew.Chem.,Int.Ed.2001,40,3284.
  • 10Smith,M.B.Organic Synthesis,McGraw-Hill,New York,1994,p.1313.

共引文献14

同被引文献59

  • 1刘云山,贝浼智,朱惠琴,李玉桂.硝基烯类化合物在有机合成中的应用[J].化学通报,1993(4):6-12. 被引量:14
  • 2Noland W E. The net'reaction[J]. Chem. Rev., 1955, 55(1) : 137 -155.
  • 3Hassner A, Namboothiri I N N. Organic syntheses based on named reactions[ M]. Elsevier, 2012.
  • 4Maity S, Naveen T, Sharma U. Stereoselective nitration of olefins with (t)BuONO and TEMPO: direct access to nitroolefins under metal-free conditions[J]. Org. Lett., 2013, 15(13) : 3384 -3387.
  • 5Ballini R, Castagnani R, Petrini M. Chemoselective synthesis of functionalized conjugated nitroalkenes[ J]. J. Org. Chem. , 1992, 57(7) : 2160 -2162.
  • 6Barrett A G M, Grabowski G G. Conjugated nitroalkenes: versatile intermediates in organic synthesis [ J ]. Chem. Rev. , 1986, 86(5) : 751 -762.
  • 7Barrett A G M. Heterosubstituted nitroalkenes in synthesis[J]. Chem. Soc. Rev. , 1991, 20(1 ) : 95 -127.
  • 8Rai A, Yadav L D S. Strategic applications of Baylis - Hillman adduets to general syntheses of 3 -nitroazetidines[J]. Org. Biomol. Chem. , 2011,9(23) : 8058 -8061.
  • 9Srivastava A, Shukla G, Nagaraju A. In( OTf )3 -catalysed one -pot versatile pyrrole synthesis through domino annulations of c~- oxoketene- N,S- acetals with nitroolefins[ J]. Org. Biomol. Chem., 2014, 12(29) : 5484-5491.
  • 10Paul S, Das A R. A new application of polymer supported, homogeneous and reusable catalyst PEG - SO3 H in the synthesis of coumarin and uracil fused pyrrole derivatives[J]. Catal. Sci. Technol., 2012, 2(6) : 1130 - 1135.

引证文献6

二级引证文献9

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