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.
[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.