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化学进展  2012 

二苯乙烯类低聚物的仿生合成

, PP. 545-555

Keywords: 二苯乙烯低聚物,酶催化,仿生合成,氧化偶联,异构化

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Abstract:

天然二苯乙烯低聚物是一类自然界分布广泛的多酚化合物,因其结构复杂且生物活性多样而受到密切关注,但此类化合物天然资源的稀少极大限制了其构效关系的调查及活性药物的筛选。近年来许多化学家对此类低聚物的仿生合成方法做了广泛而深入的研究,已形成一个新的研究热点。本文详尽综述了迄今三十多年来二苯乙烯类低聚物的仿生合成研究进展,包括在不同介质中的酶催化或金属氧化剂催化的氧化偶联方法、光催化的异构化及强酸催化下的环合反应,由不同的二苯乙烯前体通过仿生合成途径,构建出结构多样的二苯乙烯低聚物。此外,本文对该类低聚物的仿生合成研究前景做了展望。

References

[1]  李娜 (Li N), 李小妹 (Li X M), 黄开胜 (Huang K S), 林茂(Lin M). 药学学报 (Acta Pharm. Sin.), 2001, 36: 944-950
[2]  李小妹 (Li X M), 李娜 (Li N), 黄开胜(Huang K S), 林茂(Lin M). 药学学报(Acta Pharm. Sin.), 2002, 37: 69-74
[3]  Shen T, Wang X N, Lou H X. Nat. Prod. Rep., 2009, 26: 916-935
[4]  Sotheeswaran S, Pasupathy V. Phytochemistry, 1993, 32: 1083-1092
[5]  Lin M, Yao C S. Stud. Nat. Prod. Chem., 2006, 33: 601-644
[6]  Langcake P, Pryce R J. J. Chem. Soc. Chem. Commun., 1977, 208-210
[7]  Nicotra S, Cramarossa M R, Mucci A, Pagnoni U M, Riva S, Forti L. Tetrahedron, 2004, 60: 595-600
[8]  Takaya Y, Terashima K, Ito J, He Y H, Tateoka M, Yamaguchi N, Niwa M. Tetrahedron, 2005, 61: 10285-10290
[9]  李文玲(Li W L), 何侃侃(He K K), 李瀛(Li Y), 侯自杰(Hou Z J). 化学学报(Acta Chim. Sin.), 2005, 63: 1607-1612
[10]  Ponzoni C, Beneventi E, Cramarossa M R, Raimondi S, Trevisi G, Pagnoni U M, Riva S, Forti L. Adv. Synth. Catal., 2007, 349: 1497-1506
[11]  Li W L, Li H, Li Y, Hou Z J. Angew. Chem. Int. Ed., 2006, 45: 7609-7611
[12]  Ito J, Niwa M. Tetrahedron, 1996, 52: 9991-9998
[13]  Takaya Y, Yan K X, Terashima K, He Y H, Niwa M. Tetrahedron, 2002, 58: 9265-9271
[14]  Ito J, Gobaru K, Niwa M. Tetrahedron, 1998, 54: 6651-6660
[15]  Kawabata J, Mishima M, Kurihara H. Phytochemistry, 1995, 40: 1507-1510
[16]  Huang K S, Lin M, Wang Y H. Chin. Chem. Lett., 2000, 11: 1061-1062
[17]  Zhou L X, Lin M. Chin. Chem. Lett., 2000, 11: 515-516
[18]  周立新(Zhou L X), 林茂(Lin M). 药学学报(Acta Pharm. Sin.), 2000, 35: 669-674
[19]  Yao C S, Zhou L X, Lin M. Chem. Pharm. Bull., 2004, 52(2): 238-243
[20]  Sako M, Hosokawa H, Ito T, Tinuma M. J. Org. Chem., 2004, 69: 2598-2600
[21]  Takaya Y, Terashima K, Ito J, He Y H, Tateoka M, Yamaguchi N, Niwa M. Tetrahedron, 2005, 61: 10285-10290
[22]  Velu S S, Buniyamin I, Ching L K, Feroz F, Noorbatcha I, Gee L C, Awang K, Wahab I A, Weber J F F. Chem. Eur. J., 2008, 14: 11376-11384
[23]  Li W L, Luo Y L, Li H F, Zang P, Han X Q. Synthesis, 2010, 22: 3822-3826
[24]  Samaraweera U, Sotheeswaran S, Sultanbawa M U S. Phytochemistry, 1982, 21: 2585-2587
[25]  Korhammer S, Reniero F, Mattivi F. Phytochemistry, 1995, 38: 1501-1504
[26]  Aguirre J M, Alesso E N, Iglesias G Y M. J. Chem. Soc. Perkin Trans.1, 1999, 1353-1358
[27]  Li X M, Huang K S, Lin M, Zhou L X. Tetrahedron, 2003, 59: 4405-4413
[28]  Takaya Y, Yan K X, Terashima K, He H Y, Niwa M. Tetrahedron, 2002, 58: 9265-9271
[29]  Snyder S A, Zografos A L, Lin Y Q. Angew. Chem. Int. Ed., 2007, 46: 8186-8191
[30]  Jeffrey J L, Sarpong R. Tetrahedron Lett., 2009, 50: 1969-1972
[31]  Kim I, Choi J. Org. Biomol. Chem., 2009, 7: 2788-2795
[32]  Nicolaou K C, Kang Q, Wu T R, Lim C S, Chen D Y K. J. Am. Chem. Soc., 2010, 132: 7540-7548
[33]  Snyder S A, Sherwood T C, Ross A G. Angew. Chem. Int. Ed., 2010, 49: 5146-5150
[34]  Langcake P, Pryce R J. Phytochemistry, 1977, 16: 1193-1196
[35]  Donnelly D M X, Murphy F G. J. Chem. Soc. Perkin Trans 1, 1987, 2719-2722
[36]  Cichewicz R H, Kouzi S A, Hamann M T. J. Nat. Prod., 2000, 63: 29-33
[37]  He Y H, Takaya Y, Terashima K, Niwa M. Heterocycles, 2006, 68: 93-100
[38]  He S, Wu B, Pan Y J, Jiang L Y. J. Org. Chem., 2008, 73: 5233-5241
[39]  Baba K, Kido T, Kozawa M. Phytochemistry, 1994, 36: 1509-1513
[40]  Thomas N F, Lee K C, Paraidathathu T, Weber J F F, Awang K, Rondeau D, Richomme P. Tetrahedron, 2002, 58: 7201-7206
[41]  Li W L, Li H F, Luo Y L, Yang Y H, Wang N. Synlett, 2010, 8: 1247-1250
[42]  Li X C, Ferreira D. Tetrahedron, 2003, 59: 1501-1507
[43]  Takaya Y, Yan K X, Terashima K J, Ito J, Niwa M. Tetrahedron, 2002, 58: 7259-7265
[44]  Snyder S A, Breazzano S P, Ross A G, Lin Y Q, Zografos A L. J. Am. Chem. Soc., 2009, 131: 1753-1765
[45]  Nicolaou K C, Wu T R, Kang Q, Chen D Y K. Angew. Chem. Int. Ed., 2009, 48: 3440-3443

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