• 综述 •
孔令斌, 严胜骄*, 林军*. 杂环烯酮缩胺:构筑分子多样性稠杂环化合物的合成先导分子[J]. 化学进展, 2018, 30(5): 639-657.
Lingbin Kong, Shengjiao Yan*, Jun Lin*. Heterocyclic Ketene Aminals: Leading Molecules to Construct Molecular Diversity Fused Heterocyclic Compounds[J]. Progress in Chemistry, 2018, 30(5): 639-657.
中图分类号:
分享此文:
[1] Destro R, Cosentino U, Moro G, Ortoleva E, Pilati T. J. Mol Struct., 1984, 212:97. [2] Suryawanshi S N, Pandey S, Rashmirathi, Bhatt B A, Gupta S. Eur. J. Med. Chem., 2007, 42:511. [3] Maryanoff B E, Nortey J J, McNally, Sanfilippo P J, McComsey D F, Dubinsky B, Shank R P, Reitz A. Bioorg. Med. Chem. Lett., 1999, 9:1547. [4] Milczarska B, Foks H, Mikolajczyk K, Janowiec M, Zwolska Z, Andrzejczy Z. Acta Pol. Pharm., 2000, 57:307. [5] Sajadikhah S S, Maghsoodloub M T. RSC Adv., 2014, 4:43454. [6] Mizushige K, Ueda T, Yukiiri K, Suzuki H. Cardiovasc. Drug Rev., 2002, 20:163. [7] Chen L, Huang R, Du X X, Yan S J, Lin J. ACS. Sustainable Chem. Eng., 2017, 5:1899. [8] Marco E, Laine W, Tardy C, Lansiaux A, Iwao M, Ishibashi F, Bailly C, Gago F. J. Med. Chem., 2005, 48:3796. [9] Veale C G L, Zoraghi R, Young R M, Morrison J P, Pretheeban M, Lobb K A, Reiner N E, Andersen R J, Davies-Coleman M T J. Nat. Prod., 2015, 78:355. [10] Jakeman D L, Bandi S, Graham C L, Reid T R, Wentzell J R, Douglas S E. Antimicrob. Agents Ch., 2009, 53:1245. [11] Huang Z T, Wang M X. Heterocycles, 1994, 37:1223. [12] Huang Z T, Wang M X. Prog. Natural Sci., 1999, 11:971. [13] Wang K M, Yan S J, Lin J. Eur. J. Org. Chem., 2014, 2014(21):1129. [14] Gupta A K, Ila H, Junjappa H. Synthesis, 1988, 4:284. [15] Chakrabarti S, Panda K, Misra N C, Ila H, Junjappa H. Synlett, 2005. 1437. [16] Huang Z T, Liu Z R. Chem. Ber., 1989, 122:95. [17] Yu C Y, Wang L B, Li W Y, Huang Z T. Synthesis, 1996, 8:959. [18] Zhang J H, Wang M X, Huang Z T. J. Chem. Soc. Perkin Trans., 1999, 3:321. [19] Huang Z T. Synthesis, 2000, 10:1439. [20] Orlov, Kharchenko Y V. Chem. Heterocycl. Com., 2012, 48:1204. [21] Liu J, Zhang H R, Lin X R, Yan S J, Lin J. RSC Adv., 2014, 4:27582. [22] Chen X B, Liu Z C, Yang L F, Yan S J, Lin J. ACS Sustainable Chem. Eng., 2014, 2:1155. [23] Chen X B, Yan S J, Lin J. Tetrahedron, 2015, 71:4745. [24] Chen X B, Wang X Y, Zhu D D, Yan S J, Lin J. Tetrahedron, 2014, 70:1047. [25] Yan S J, Chen Y L, Liu L, Tang Y J, Lin J. Tetrahedron Lett., 2011, 52:465. [26] Xu S, Li Z. Eur. J. Org. Chem., 2014, 28:6210. [27] Chen N, Meng X Q, Zhu F J, Cheng J, Shao X S, Li Z. J. Agric. Food Chem., 2015, 63:1360. [28] Liu X M, Lin X R, Yan S J, Peng M Y, Huang R, Lin J. Tetrahedron, 2016, 72:5314. [29] Chen X B, Liu Z C, Lin X R, Huang R, Yan S J, Lin J. ACS Sustainable Chem. Eng., 2014, 2:2391. [30] Fan J, Yang Q Y, He G J, Xie X G, Zhu H Y, Jin Y, Lin J. RSC Adv., 2014, 4:28852. [31] Zhang J H, Wang M X, Huang Z T. J. Chem. Soc. Perkin Trans. 1999, 1:2087. [32] Sharon A, Maulik P R, Roy R, Ram V. Tetrahedron Lett., 2004, 45:5815. [33] 彭美阳(Peng M Y),杨瑞霞(Yang R X),刘昔敏(Liu X M),严胜骄(Yan S J),林军(Lin J).有机化学(Chin.J.Org.Chem.), 2015, 35:1754. [34] Yaqub M, Yu C Y, Jia Y M, Huang Z T. Synlett, 2008, 9:1357. [35] Xu W Y, Jia Y M, Yang J K, Huang Z T, Yu C Y. Synlett, 2010, 11:1682. [36] Wen L R, Liu C, Li M, Wang L J. J. Org. Chem., 2010, 75:7605. [37] Li M, Shao P, Wang S W, Kong W, Wen L R. Eur. J. Org. Chem., 2012, 77:8956. [38] Wen L R, Li Z R, Li M, Cao H. Green Chem., 2012, 14:707. [39] Huang Z T, Liu Z R. Heterocycles, 1986, 24:2247. [40] Yu C Y, Yang P H, Zhao M X, Huang Z T. Synlett, 2006, 12:1835. [41] Sriparna C, Kausik K, Hiriyakkanavar J. Synlett, 2005, 9:1437. [42] Li M, Zhou Z M, Wen L R, Qiu Z X. J. Org. Chem., 2011, 76:3054. [43] Wang Z W, Sun T Q, Chen J, Deng H M, Shao M, Zhang H, Cao W G. Tetrahedron, 2013, 69:4270. [44] Yao C S, Xiao Z X, Xie Y W, Li T J, Wang S, Liu R, Yu C X. RSC Adv., 2013, 3:10801. [45] Yan S J, Niu Y F, Huang R, Lin J. Synlett, 2009, 2009(17):2821. [46] Hu L, Wang K M, Zhao M, Lin X R, Zhu H Y, Yan S J, Lin J. Tetrahedron, 2014, 70(30):4478. [47] Liu J, Yan S J, Cao Z M, Cui S S, Lin J. RSC Adv., 2016, 6:103057. [48] Yildirim M, Evis N, Knight D W, Kariuki B M. Tetrahedron, 2014, 70:5674. [49] Yan S J, Chen Y L, Liu L, He N Q, Lin J, Green Chem., 2010, 12:2043. [50] Yu F C, Yan S J, Huang R, Tang Y J, Lin J. RSC Adv., 2011, 1:596. [51] Zhu D D, Chen X B, Huang R, Yan S J, Lin J. Tetrahedron, 2015, 71:2363. [52] Wang K M, Ma Y L, Lin X R, Yan S J, Lin J. RSC Adv., 2015, 5:36472. [53] Rezvanian A. Tetrahedron, 2015, 71:4752. [54] Zhang J H, Wang M X, Huang Z T. Tetrahedron Lett., 1998, 39:9237. [55] Sharon A, Prantap R, Maulik P R, Ram V J. Tetrahedron, 2005, 61:3781. [56] 严胜骄(Yan S J),林军(Lin J). 有机化学(Chin. J. Org. Chem.), 2010, 30, 465. [57] Ma Y L, Wang K M, Lin X R, Yan S J, Lin J. Tetrahedron, 2014, 70:6578. [58] Chen X B, Zhu L, Fang L, Yan S J, Lin J. RSC Adv., 2014, 4:9926. [59] Yu F C, Chen Z Q, Hao X P, Yan S J, Huang R, Lin J. RSC Adv., 2014, 4, 6110. [60] 陈亮(Chen L),王保取(Wang B Q),赵宇宸(Zhao Y C),严胜骄(Yan S J),林军(Lin J).有机化学(Chin. J. Org. Chem.), 2017, 37:1433. [61] Chen L, Huang R, Du X X, Yan S J, Lin J. ACS Sustainable Chem., Eng., 2017, 5:1899. [62] Savych I, Ejaz S A, Iqbal J, Abbasi A, Langer P. Eur. J. Org. Chem., 2017, 2017(24):186. [63] Guo W S, Xin X, Zhao K L, Wen L R, Li M. RSC Adv., 2015, 5:70429. [64] Sun F L, Shao X S, Li Z. RSC Adv., 2016, 6:15382. [65] Yang L J, Yan S J, Chen W, Lin J. Synthesis, 2010, 2010(20):3536. [66] Yu F C, Hao X P, Lin X R, Yan S J, Lin J. Tetrahedron, 2015, 71:4084. [67] Zhou B, Liu Z C, Qu W W, Yang R, Lin X R, Yan S J, Lin J. Green Chem., 2014, 16:4359. [68] Liu T, Zhu H Y, Luo D Y, Yan S J, Lin J. Molecules, 2016, 21:638. [69] Liao J P, Zhang T Y, Chu Y, Huang Z T. Synlett, 2007, 5:761. [70] Yaqub M, Perveen R, Shafiq Z, Pervez H, Tahir M. Synlett, 2012, 23:1755. [71] Wen L R, Sun Q C, Zhang H L, Li M. Org. Biomol. Chem., 2013, 11:781. [72] Yan S J, Huang C, Su C X, Ni Y F, Lin J. J. Comb. Chem., 2010, 12:91. [73] Huang C, Yan S J, Zeng X H, Dai X Y, Zhang Y, Qing C, Lin J. Eur. J. Med. Chem., 2011, 46:1172. [74] Yu F C, Yan S J, Hu L, Wang Y C, Lin J. Org. Lett., 2011, 18:4782. [75] Terrett N K. Comb. Chem., 2012, 14:5. [76] Wilson L, Zhao W Y, Zhao D B, Desai A A, Guizzetti S, Laird T. Org. Process Res. Dev., 2012, 16:526. [77] Pakravan1 P, Kashanian S, Khodaei M M, Harding F J. Pharmacolo. Rep., 2013, 65:313. [78] Peng H Y. Res. Chem. Intermediat., 2016, 42:5617. [79] Jiang B, Wang X, Li M Y, Wu Q, Ye Q, Xu H W Tu S J. Org. Biomol. Chem., 2012, 10:8533. [80] Wang H Y, Li L L, Lin W, Xu P, Huang Z B, Shi D Q. Org. Lett., 2012, 14:4598. [81] Xu H, Zhou B, Zhou P, Zhou J, Shen Y H, Yu F C, Lu L L. Chem. Commun., 2016, 52:8002. [82] Zhang Y C, Liu Z C, Yang R, Zhang J H, Yan S J, Lin J. Org. Biomol. Chem., 2013, 11:7276. [83] Wen L R, Jin X J, Niu X D, Li M. J. Org. Chem., 2015, 80:90. [84] Bayat M, Hosseini F, Notash B. Tetrahedron Lett., 2016, 57:5439. [85] 王保取(Wang B Q), 孔令斌(Kong L B), 罗琴(Luo Q), 严胜骄(Yan S J). 有机化学(Chin. J. Org. Chem.), 2017, 37:2972. [86] Wen L R, Sun Q C, Zhang H L, Li M. Org. Biomol.Chem., 2013, 11:781. [87] Yu F C, Huang R, Ni H C, Fan J, Yan S J, Lin J. Green Chem., 2013, 15:453. [88] Chen X B, Liu X M, Huang R, Yan S J, Lin J. Eur. J. Org. Chem., 2013, 2013(21):4607. [89] Fan Y F, Liu S, Chen N Y, Shao S H, Xu X Y, Li Z. Synlett, 2015, 26:393. [90] Ma Y L, Wan K M,Huang R, Lin J, Yan S J. Green Chem., 2017, 19:3574. [91] Huang Z T, Wang M X. J. Org. Chem., 1992, 57:184. [92] Gu J W, Xiong W T, Zhang Z H, Zhu S Z. Synthesis, 2011, 11:1717. [93] Wang H. Synth. Commun., 1991, 21:1167. [94] Wang H. Synth. Commun., 1991, 21:1909. [95] Wang B Q, Luo Q, Xiao Q, Lin J, Yan S J. ACS Sustainable Chem. Eng., 2017, 5:2391. [96] Cui S S, Huang R, Luo D Y, Yan S J, Lin J. Eur. J. Org. Chem., 2017, 2017(24):3442. [97] Du X X, Huang R, Yang C L, Lin J, Yan S J. RSC Adv., 2017, 7:40067. [98] Yu F Y, Lin X R, Liu Z C, Zhang J H, Liu F F, Wu W, Ma Y L, Qu W W, Yan S J, Lin J. ACS Omega, 2017, 2:873. |
[1] | 刘刚,恽榴红,王建新. 组合化学、分子库与新药研究[J]. 化学进展, 1997, 9(03): 223-. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||