综述与进展

酰胺官能团构建方法研究新进展

  • 盛国柱 ,
  • 张炜
展开
  • 青岛农业大学化学与药学院 青岛 266109

收稿日期: 2013-05-29

  修回日期: 2013-07-02

  网络出版日期: 2013-07-26

基金资助

山东省自然科学基金(No. ZR2012CL15)资助项目.

New Advances of the Methods of Amide Function Group for Construction

  • Sheng Guozhu ,
  • Zhang Wei
Expand
  • College of Chemistry and Drug, Qingdao Agruicultural University, Qingdao 266109

Received date: 2013-05-29

  Revised date: 2013-07-02

  Online published: 2013-07-26

Supported by

Project supported by the Natural Science Foundation of Shandong Province (No. ZR2012CL15).

摘要

酰胺是广泛存在于天然产物及合成药物中的一种重要的功能基团,对其合成方法的研究具有重要意义,也是现在合成方法研究的一个热点. 就近几年关于酰胺合成方法做简要总结,以期对以后的研究具有一定意义.

本文引用格式

盛国柱 , 张炜 . 酰胺官能团构建方法研究新进展[J]. 有机化学, 2013 , 33(11) : 2271 -2282 . DOI: 10.6023/cjoc201305048

Abstract

Amides are one of the most ubiquitous and important functional groups in natural products and synthetic drugs. The research of forming methods for amide is of great significance, also it is now a hotspot in the research of the synthetic method. Herein, the synthetic methods of amides in recent years are reviewed, which is of great significance for future research.

参考文献

[1] Ishihara,K.; Ohara,S.; Yamamoto,H.J.Org.Chem.1996,61,4196.

[2] Nguyen,T.B.; Sorres,J.; Tran,M.Q.; Ermolenko,L.; Al-Mourabit,A.Org.Lett.2012,14,3202.

[3] Charville,H.; Jackson,D.; Hodges,G.; Whiting,A.Chem.Commun.2010,46,1813.

[4] Starkov.P,Sheppard.T.D.Org.Biomol.Chem.2011,9,1320.

[5] Mali,S.M.; Jadhav,S.V.; Gopi,H.N.Chem.Commun.2012,48,7085.

[6] Li,M.; Hu,L.; Cao,X.Q.; Hong,H.Y.; Lu,J.M.; Gu,H.W.Chem.Eur.J.2011,17,2763.

[7] Ghaffarzadeh,M.; Joghan,S.S.; Faraji,F.Tetrahedron Lett.2012,53,203.

[8] Zhu,C.L.; Zou,X.F.J.Zhejiang Normal Univ.(Nat.Sci.) 2004,27,261 (in Chinese).

(祝春兰,邹雪飞,浙江师范大学学报(自然科学版),2004,27,261.)

[9] Shi,F.; Li,J.; Li,C.J.; Jia,X.S.Tetrahedron Lett.2010,51,6049.

[10] Cho,D.H.; Jang,D.O.Tetrahedron Lett.2004,45,2285.

[11] Ohshima,T.; Hayashi,Y.; Agura,K.; FujⅡ,Y.; Yoshiyama,A.; Mashima,K.Chem.Commun.2012,48,5434.

[12] Wahba,A.E.; Peng,J.N.; Hamann,M.T.Tetrahedron.Lett.2009,50,3901.

[13] Li,G.; Wang,X.W.; Tian,C.; Zhang,T.B.; Zhang,Z.L.; Liu,J.Y.Tetrahedron Lett.2012,53,5193.

[14] Bhattacharya,A.; Suarez,V.; Jr.,V.T.; Wu,J.J.Tetrahedron Lett.2006,47,3221.

[15] Comerford,J.W.; Clark,J.H.; Macquarrie,D.G.; Breeden,S.W.Chem.Commun.2009,18,2562.

[16] Markó,I.E.; Mekhalfia,A.Tetrahedron Lett.1990,31,7237.

[17] Liu,Z.J.; Zhang,J.; Chen,S.L.Angew.Chem.,Int.Ed.2012,51,3231.

[18] Kekeli E.K.; Wolf,C.Org.Lett.2007,9,3429.

[19] Prasad,V.; Kale,R.R.; Mishra,B.B.; Kumar,D.; Tiwari,V.K.Org.Lett.2012,14,2936.

[20] Wang,X.B.; David; Wang,Z.G.Tetrahedron 2011,67,3406.

[21] Shaw,A.Y.; Denning,C.R.; Hulme,C.Tetrahedron Lett.2012,53,4151.

[22] Ramesh,K.; Murthy,S.N.; Karnakar,K.; Reddy,K.H.V.; Nageswar,Y.V.D.; Vijay,M.; Devi,B.P.; Prasad,R.Tetrahedron Lett.2012,53,2636.

[23] Colombeau,L.; Traoré,T.; Compain P.; Martin,O.R.J.Org.Chem.2008,73,8647.

[24] Tamaru,Y.; Yamada,Y.; Yoshida,Z.Synthesis 1983,474.

[25] Suto,Y.; Yamagiwa,N.; Torisawa,Y.Tetrahedron Lett.2008,49,5732.

[26] Ghosh,S.C.; Ngiam,J.S.Y.; Chai,C.L.L.; Seayad,A.M.; Dang,T.T.; Chen,A.Q.Adv.Synth.Catal.2012,354,1407.

[27] Yoo,W.J.; Li,C.J.J.Am.Chem.Soc.2006,128,13064.

[28] Ghosh,S.C.; Ngiam,J.S.Y.; Seayad,A.M.; Tuan,D.T.; Chai,C.L.L.; Chen,A.Q.J.Org.Chem.2012,77,8007.

[29] Zhang,C.; Xu,Z.J.; Zhang L.R.; Jiao,N.Angew.Chem.,Int.Ed.2011,50,11088.

[30] Zhang,C.; Zong,X.L.; Zhang,L.R.; Jiao,N.Org.Lett.2012,14,3280.

[31] Zhu,M.W.; Fujita,K.; Yamaguchi,R.J.Org.Chem.2012,77,9102.

[32] Cadoni,R.; Porcheddu,A.; Giacomelli,G.; Luca,L.D.Org.Lett.2012,14,5014.

[33] Chang,J.W.W.; Ton,T.M.U.; Tania,S.; Taylor,P.C.; Chan,P.W.H.Chem.Commun.2010,46,922.

[34] Qin,Y.C.; Peng,Q.; Song,J.S.; Zhou,D.Tetrahedron Lett.2011,52,5880.

[35] Gai,L.L.,Kung K.K.Y.; Wong,M.K.Chem.Commun.2012,48,4112.

[36] Allam,B.K.; Singh,K.N.Tetrahedron Lett.2011,52,5851.

[37] Zhang,L.J.; Wang,S.W.; Zhou,S.L.; Yang,G.S.; Sheng,E.H.J.Org.Chem.2006,71,3149.

[38] Seo,S.Y.; Marks,T.J.Org.Lett.2008,10,317.

[39] Thomson,J.A.; Schafer,L.L.Dalton Trans.2012,7897.

[40] Qian,C.W.; Zhang,X.M.; Li,J.M.; Xu,F.; Zhang,Y.; Shen,Q.Organometallics 2009,28,3856.

[41] Li,J.M.; Xu,F.; Zhang,Y.; Shen,Q.J.Org.Chem.2009,74,2575.

[42] CAI C.Y.; Li,L.; Xu,F.; Shen,Q.Chin.Sci.Bull.2010,55,3641.

[43] Xu,B.; Huang,L.L.; Yang,Z.J.; Yao,Y.M.; Zhang,Y.; Shen,Q.Organometallics 2011,30,3588.

[44] Xu,K.; Hu,Y.B.; Zhang,S.; Zha,Z.G.; Wang,Z.Y.Chem.Eur.J.2012,18,9793.

[45] Naota,T.; Murahashi,S.I.Synlett 1991,693.

[46] Nordstrøm,L.U.; Vogt,H.; Madsen,R.J.Am.Chem.Soc.2008,130,17672.

[47] Ghosh,S.C.; Muthaiah,S.; Zhang,Y.; Xu,X.Y.; Hong,S.H.Adv.Synth.Catal.2009,351,2643.

[48] Zhang,Y.; Chen,C.; Ghosh,S.C.; Li,Y.X.; Hong,S.H.Organometallics 2010,29,1374.

[49] Maki,B.E.; Scheidt,K.A.Org.Lett.2009,11,1651.

[50] Gunanathan,C.; Ben-David,Y.; Milstein,D.Science 2007,317,790.

[51] Zhu,J.L.; Zhang,Y.; Shi,F.; Deng,Y.Q.Tetrahedron Lett.2012,53,3178.

[52] Chen C.; Hong,S.H.Org.Lett.2012,14,2992.

[53] Xiao,F.H.; Liu,Y.; Tang,C.L.; Deng,G.J.Org.Lett.2012,14,984.

[54] Das,R.; Chakraborty,D.Catal.Commun.2012,26,48.

[55] Chan,W.K.; Ho,C.M.; Wong,M.K.; Che,C.M.J.Am.Chem.Soc.2006,128,14796.

[56] Cho,S.H.; Yoo,E.J.; Bae,I.; Chang,S.J.Am.Chem.Soc.2005,127,16046.

[57] Wei,W.; Hu,X.Y.; Yan,X.W.; Zhang,Q.; Cheng,M.; Ji,J.X.Chem.Commun.2012,48,305.

[58] Shen,B.; Makley,D.M.; Johnston,J.N.Nature 2010,465,1027.

文章导航

/