English
新闻公告
More
化学进展 2010, Vol. 22 Issue (07): 1233-1241 前一篇   后一篇

• 特约稿 •

“水上” (“on water”) 有机反应*

刘利**   王东   

  1. (北京国家分子科学实验室  中国科学院化学所  中科院分子识别和功能重点实验室    北京 100190)
  • 收稿日期:2010-02-05 出版日期:2010-07-24 发布日期:2010-07-02
  • 通讯作者: 刘利 E-mail:lliu@iccas.ac.cn
  • 基金资助:

    国家爱自然科学基金;科技部“重大新药创制”国家科技重大专项;中科院方向性项目

Organic Reactions "on Water"

Liu Li**    Wang Dong   

  1. (CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China)
  • Received:2010-02-05 Online:2010-07-24 Published:2010-07-02

“水上”有机反应的发展是水相绿色合成反应研究领域中的一个突破。体系的非均相性质是“水上”反应的基本特征。水不仅是重要的绿色的反应介质,在大多数“水上”有机反应中都能观察到水对反应的速度和选择性有明显的提升作用。采用“水上”反应的条件,可以使反应的规模扩大,有利于产物的分离、纯化。本文以反应的类型分类综述了近年来有关“水上”有机反应研究的进展,以及在绿色有机合成中的应用。

The development of “on water” organic reaction is a breakthrough in the field of aqueous organic reactions for green synthesis. An essential characteristic of “on water” reaction is heterogeneity of the reaction system. Water is not only used as a green reaction media, but also, in most “on water” reactions, plays a crucial role in observing large rate acceleration and selectivity enhancement. Under “on water” reaction conditions, the reaction can be scaled-up and the procedure is favorable to make a clear phase separation. The recent advancements of “on water”organic reaction and its applications in green organic synthesis are reviewed in terms of classification of organic reaction.

Contents 
1 Introduction 
2 Cycloaddition reaction on water 
3 Nucleophilic addition reaction on water 
3.1 Conjugate addition 
3.2 Nucleophilic addition to carbonyl groups 
3.3 Au-catalyzed tandem reaction 
3.4 Enantioselective direct aldol reaction 
4 Nucleophilic substitution reaction on water 
5 Coupling reaction on water 
5.1 Transition metal-catalyzed coupling reaction 
5.2 Dehydrogenative coupling reaction 
6 Oxidation on water 
7 Bromination reaction on water 
8 Theoretical studies 
9 Conclusion

中图分类号: 

()

[1 ] Grieco A. Organic Synthesis in Water. London: Black Academic
& Professional,1998
[2 ] Li C J,Chan T H. Comprehansive Organic Reaction in Aqueous
Media. NY: John Wiley & Sons,Inc. Hoboken,2007
[3 ] Rideout D C,Breslow R. J. Am. Chem. Soc. ,1980,102:
7816—7817
[4 ] Narayan S,Muldoon J,Finn M G,Fokin V V,Kolbe H C,
Sharpless K B. Angew. Chem. Int. Ed. ,2005,44: 3275—
3279
[5 ] Chanda A,Fokin V V. Chem. Rev. ,2009,109: 725—748
[6 ] González-Cruz D,Tejedor D,de Armas P,García-Tellado F.
Chem. Eur. J. ,2007,13: 4823—4832
[7 ] González-Cruz D, Tejedor D, de Armas P, Moralesa E Q,
García-Tellado F. Chem. Commun. ,2006,2798—2800
[8 ] Ranu B C,Banerjee S. Tetrahedron Lett. ,2007,48: 141—143
[9 ] Zheng Z,Perkin B L,Ni B. J. Am. Chem. Soc. ,2010,132:
50—51
[10] Kumaravel K,Vasuki G. Green Chem. ,2009,11: 1945—1947
[11] Shaabani A,Rahmati A,Farhangi E. Tetrahedron Lett. ,2007,
48: 7291—7294
[12] Chakraborti A K, Rudrawar S, Jadhav K B, Kaur G,
Chankeshwara S V. Green Chem. ,2007,9: 1335—1340
[13] Liu X Y,Che C M. Angew. Chem. Int. Ed. ,2008,47:
3805—3810
[14] Guizzetti S,Benaglia M,Raimondi L,Celentano G. Org. Lett. ,
2007,9: 1247—1250
[15] Huang J,Zhang X,Armstrong D W. Angew. Chem. Int. Ed. ,
2007,46: 9073—9077
[16] Cozzi P G,Zoli L. Green Chem. ,2007,9: 1292—1295
[17] Cozzi P G,Zoli L. Angew. Chem. Int. Ed. ,2008,47: 4162—
4166
[18] Fleckenstein C A,Plenio H. Green Chem. ,2007,9: 1287—
1291
[19] Turner G L,Morris J A,Greaney M F. Angew. Chem. Int.
Ed. ,2007,46: 7996—8000
[20] Carril M,SanMartin R,Tellitu I,Domínguez E. Org. Lett. ,
2006,8: 1467—1470
[21] Wei C M,Li C J. J. Am. Chem. Soc. ,2003,125: 9584—
9585
[22] Chung L L,Yang J,Wei Y,Ying J Y. Adv. Synth. Catal. ,
2009,351: 2887—2896
[23] Huang B S,Yao X Q,Li C J. Adv. Synth. Catal. ,2006,348:
1528—1532
[24] Yan B,Liu Y. Org. Lett. ,2007,9: 4323—4326
[25] Zhang H B,Liu L,Chen Y J,Wang D,Li C J. Eur. J. Org.
Chem. ,2006,869—873
[26] Zhang H B,Liu L,Chen Y J,Wang D,Li C J. Adv. Synth.
Catal. ,2006,348: 229—235
[27] Wallis P J,Booth K J,Pattiab A F,Scott J L. Green Chem. ,
2006,8: 333—337
[28] Li H J,Zhao J L,Chen Y J,Liu L,Wang D,Li C J. Green.
Chem. ,2005,7: 61—63
[29] Shapiro N,Vigalok A. Angew. Chem. Int. Ed. ,2008,47:
2849—2852
[30] Pirrung M C,Das Sarma K. J. Am. Chem. Soc. ,2004,126:
444—445
[31] Podgorek A,Stavber S,Zupanb M,Iskra J. Tetrahedron Lett. ,
2006,47: 1097—1099
[32] Podgorek A,Stavber S,Zupanab M,Iskra J. Green Chem. ,
2007,9: 1212—1218
[33] Pirrung M C. Chem. Eur. J. ,2006,12: 1312—1317
[34] Jung Y,Marcus R A. J. Am. Chem. Soc. ,2007,129: 5492—
5502

[1] 丁奇峰, 杨雅琼, 缪文俊, 黄和, 于杨*, 黄菲*. 基于N,S-缩烯酮的杂环合成的研究[J]. 化学进展, 2018, 30(11): 1615-1623.
[2] 朱映光 翟昌伟 胡文浩. 不对称多组分反应[J]. 化学进展, 2010, 22(07): 1380-1396.
[3] 王琦芳,宋肖锴,颜朝国. 丙二腈在多组分反应中的应用* [J]. 化学进展, 2009, 21(05): 997-1007.
[4] 孙宏元,郝爱友,尹明静,张华承,申健. 环糊精在绿色有机合成中的应用[J]. 化学进展, 2008, 20(11): 1694-1698.
阅读次数
全文


摘要

“水上” (“on water”) 有机反应*