中文   |   English   |   Email Alert

酰胺类化合物的高效合成研究

熊兴泉*, 范观铭, 朱荣俊, 石霖, 肖上运, 毕成

化学进展 ›› 2016, Vol. 28 ›› Issue (4) :497-506

PDF (1226KB)
化学进展 ›› 2016, Vol. 28 ›› Issue (4) :497-506 DOI: 10.7536/PC150718
综述与评论
扫码查看或转发全文

酰胺类化合物的高效合成研究

    熊兴泉*, 范观铭, 朱荣俊, 石霖, 肖上运, 毕成
作者信息 +

Highly Efficient Synthesis of Amides

  • Xiong Xingquan*, Fan Guanming, Zhu Rongjun, Shi Lin, Xiao Shangyun, Bi Cheng
Author information +
文章历史 +

摘要

酰胺类化合物是有机化学中最常见的化合物之一, 在药物化学、生物化学以及高分子合成等领域都有着重要的应用. 近年来高效合成酰胺类化合物已经成为一个研究热点, 具有重要的意义.本文主要从过渡金属催化、有机小分子催化等方面讨论近几年来酰胺类化合物的合成研究进展, 并对其发展趋势进行展望.

Abstract

Amides have been one of the most popular compounds in organic chemistry. There are plenty of important applications in many fields such as medicinal chemistry, biochemistry and polymer synthesis. Highly efficient synthesis of amides has become a hot topic in recent years. In this review, the application of transition metal catalysis and small molecule organocatalysis in the synthesis of amides in the last few years is briefly summarized, and the prospects of the synthesis of amides are also discussed.

Contents
1 Introduction
2 Amides synthesis of transition metal
2.1 Synthesis of amides by gold catalysts
2.2 Synthesis of amides by ruthenium-based catalysts
2.3 Synthesis of amides by copper catalysts
2.4 Synthesis of amides by iron and nickel catalysts
2.5 Synthesis of amides by palladium catalysts
3 Synthesis of amides by small molecule organic catalysts
4 Synthesis of amides by other methods
5 Conclusion

关键词

酰胺化合物 / 过渡金属催化 / 有机小分子催化 / 绿色合成

Key words

amides / transition metal catalysis / small molecule organocatalysis / green synthesis

引用本文

引用格式 ▾
熊兴泉, 范观铭, 朱荣俊, 石霖, 肖上运, 毕成. 酰胺类化合物的高效合成研究[J]. 化学进展, 2016, 28(4): 497-506 DOI:10.7536/PC150718
Xiong Xingquan, Fan Guanming, Zhu Rongjun, Shi Lin, Xiao Shangyun, Bi Cheng. Highly Efficient Synthesis of Amides[J]. Progress in Chemistry, 2016, 28(4): 497-506 DOI:10.7536/PC150718

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1] Chitra S, Vishal K, Upendra S, Neeraj K, Bikram S. Current Organic Synthesis, 2013, 10: 241.
[2] 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.
[3] Nordstrøm L U, Vogt H, Madsen R. J. Am. Chem. Soc., 2008, 130: 17672.
[4] Cadoni R, Porcheddu A, Giacomelli G, Luca L D. Org. Lett., 2012, 14: 5014.
[5] Allen C L, Williams J M. J. Chem. Soc. Rev., 2011, 40, 3405.
[6] Klitgaard S K, Egeblad K, Mentzel U V, Popov A G, Jensen T, Taarning E, Nielsen I S, Christensen C H. Green Chem., 2008, 10: 419.
[7] Wang Y, Zhu D P, Tang L, Wang S J, Wang Z Y. Angew. Chem Int. Ed., 2011, 123: 9079.
[8] Francois S J, Miyamura H, Kobayashi S. J. Am. Chem. Soc., 2011, 133: 18550.
[9] Zhu J L, Zhang Y, Shi F, Deng Y Q. Tetrahedron Lett., 2012, 53: 3178.
[10] Kegnæs S, Mielby J, Mentzel U V, Jensen T, Fristrup P, Riisager A. Chem. Commun., 2012, 48: 2427.
[11] Tanaka S, Minato T, Ito E, Hara M, Kim Y, Yamamoto Y, Asao N. Chem. Eur. J., 2013, 19: 11832.
[12] Guo X F, Tang L, Yang Y, Zha Z G, Wang Z Y.Green Chem., 2014, 16: 2443.
[13] Chng L L, Yang J H, Ying J Y. ChemSusChem, 2015, 8: 1916.
[14] Li F, Ma J, Lu L, Bao X F, Tang W Y. Catal. Sci. Technol., 2015, 5: 1953.
[15] Gunanathan C, Milstein D. Science, 2007, 317: 790.
[16] Zhang J, Leitus G, Ben-David Y, Milstein D. J. Am. Chem. Soc., 2005, 127: 10840.
[17] Gnanaprakasam B, Milstein D. J. Am. Chem. Soc., 2011, 133: 1682.
[18] Srimani D, Balaraman E, Hu P, Ben-David Y, Milstein D. Adv. Synth. Catal., 2013, 355: 2525.
[19] Han Q, Xiong X Q, Li S Z. Catal. Commun., 2015, 58: 85.
[20] Nordstrøm L U, Vogt H, Madsen R. J. Am. Chem. Soc., 2008, 130: 17672.
[21] Ghosh S C, Muthaiah S, Zhang Y, Xu X Y, Hong S H. Adv. Synth. Catal., 2009, 351: 2643.
[22] Chen, C, Zhang Y, Hong S H. J. Org. Chem., 2011, 76: 10005.
[23] Malineni J, Merkens C, Keul H, Möller M. Catal. Commun., 2013, 40: 80.
[24] Zhu M W, Fujita K, Yamaguchi R. J. Org. Chem., 2012, 77: 9102.
[25] Qu G R, Song Y W, Niu H Y, Guo H M, Fossey J S. RSC Adv., 2012, 2: 6161.
[26] Li X Y, Li Z K, Deng H, Zhou X G. Tetrahedron Lett., 2013, 54: 2212.
[27] Yang S Z, Yan H, Ren X Y, Shi X K, Li J, Wang Y L, Huang G S. Tetrahedron, 2013, 69: 6431.
[28] Xie Y X, Song R J, Yang X H, Xiang J N, Li J H. Eur. J. Org. Chem., 2013, 5737.
[29] Mali S M, Bhaisare R D, Gopi H N. J. Org. Chem., 2013, 78: 5550.
[30] Qin C, Zhou W, Chen F, Ou Y, Jiao N. Angew. Chem. Int. Ed., 2011, 50: 12595.
[31] Porcheddua A, Luca L D. Adv. Synth. Catal., 2012, 354: 2949.
[32] 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.
[33] Whittaker A M, Dong V M. Angew. Chem. Int. Ed. 2015, 54:1312.
[34] Martinelli J R, Clark T P, Watson D A, Munday R H, Buchwald S L. Angew. Chem. Int. Ed., 2007, 46: 8460.
[35] Ren W, Yamane M. J. Org. Chem., 2009, 74: 8332.
[36] Dang T T, Zhu Y H, Ngiam J S Y, Ghosh S C, Chen A Q, Seayad A M. ACS Catal., 2013, 3: 1406.
[37] List B, Lerner R A, Barbas C F. J. Am. Chem. Soc., 2000, 122: 2395.
[38] Vora H U, Rovis T. J. Am. Chem. Soc., 2007, 129: 13796.
[39] Sabot C, Kumar K A, Meunier S, Mioskowski C. Tetrahedron Lett., 2007, 48: 3863.
[40] Sanz R, Martínez A, Guilarte V, Gutiérrez J M A, Rodríguez F. Eur. J. Org. Chem., 2007, 4642.
[41] Yang X, Birman V B. Org. Lett., 2009, 11: 1499.
[42] Vanjari R, Guntreddi T, Singh K N. Green Chem., 2014, 16: 351.
[43] Lanigan R M, Starkov P, Sheppard T D. J. Org. Chem., 2013, 78: 4512.
[44] Chen Z K, Fu R Z, Chai W, Zheng H, Sun L, Lu Q, Yuan R X. Tetrahedron, 2014, 70: 2237.
[45] Kumari S, Shekhar A, Mungse H P, Khatri O P, Pathak D D. RSC Adv., 2014, 4: 41690.
PDF (1226KB)

4799

访问

0

被引

详细

导航
相关文章

/

〈 〉