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知识介绍
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| 有机硒催化的最新进展 |
| 俞磊 |
| 扬州大学化学化工学院 江苏扬州 225002 |
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| Recent Progresses in Organoselenium Catalysis |
| YU Lei |
| School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China |
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摘要：有机硒催化是有机硒化学的前沿研究领域之一。有机硒催化的氧化反应普遍使用清洁的过氧化氢作氧化剂，可用于开发绿色合成新工艺。除此之外，对有机硒催化反应的研究还能够发现新的化学反应，从而为有机合成提供新工具。对这一领域近3年来的进展，作了简要的介绍。
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| 关键词： 有机硒,
催化,
有机合成,
绿色化学
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| 基金资助:国家自然科学基金（21202141）；江苏省优势学科项目（PAPD）资助 |
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通讯作者:
俞磊
E-mail: yulei@yzu.edu.cn
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| 引用本文: |
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俞磊. 有机硒催化的最新进展[J]. 化学教育（中英文）, 2016, 37(16): 1-4
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| [1] |
彭祚全,黄剑锋. 世界硒都恩施硒资源研究概述. 北京:清华大学出版社,2012
|
| [2] |
Riley H L,Morley J F,Friend N A C. Journal of the Chemical Society,1932:1875-1883
|
| [3] |
Sharpless K B,Lauer R F,Teranishi A Y. Journal of the American Society,1973,95(18):6137-6139
|
| [4] |
Hori T,Sharpless K B. Journal of Organic Chemistry,1979, 44(23):4204-4208
|
| [5] |
Hori T,Sharpless K B. Journal of Organic Chemistry,1979, 44(23):4208-4210
|
| [6] |
ten Brink G J,Fernandes B C M,van Vliet M C A. et. al. Journal of the Chemical Society. Perkin Transactions 1,2001(3):224-228
|
| [7] |
Santoro S,Santi C,Sabatini M. et al. Advanced Synthesis & Catalysis,2008,350(18):2881-2884
|
| [8] |
Mellegaard S R,Tunge J A. Journal of Organic Chemistry,2004,69(25):8979-8981
|
| [9] |
Tiecco M,Testaferri L,Tingoli M. et al. Journal of Organic Chemistry,1990,55(15):4523-4528
|
| [10] |
ten Brink G J,Vis J M,Arends I W C E. et al. Journal of Organic Chemistry,2001,66(7):2429-2433
|
| [11] |
ten Brink G J,Vis J M,Arends I W C E. et al. Tetrahedron,2002,58(20):3977-3983
|
| [12] |
Zhao D,Johansson M,Bäckvall, J E. European Journal of Organic Chemistry, 2007(26):4431-4436
|
| [13] |
Freudendahl D M,Santoro S,Shahzad,S A. et al. Angewandte Chemie International Edition,2009,48(45):8409-8411
|
| [14] |
Santi C,Santoro S,Battistelli B. Current Organic Chemistry,2010,14(20):2442-2462
|
| [15] |
Santoro S,Azeredo J B,Nascimento V. et al. RSC Advances,2014,4(60):31521-31535
|
| [16] |
Breder A,Ortgies S. Tetrahedron Letters,2015,56(22):2843-2852
|
| [17] |
Ml-ochowski J,Wójtowicz-Ml-ochowska H. Molecules, 2015,20(6):10205-10243
|
| [18] |
俞磊,王俊,陈天,等. 有机化学,2013,33(5):1096-1099
|
| [19] |
Yu L,Wang J,Chen T. et al. Applied Organometallic Chemistry,2014,28(8):652-656
|
| [20] |
Yu L,Cheng F,Ding K. ChemCatChem,2016,8(6):1033-1037
|
| [21] |
Yu L,Wu Y,Cao H.et al. Green Chemistry,2014,16(1):287-293
|
| [22] |
Zhang X,Ye J,Yu L. et al. Advanced Synthesis & Catalysis,2015,357(5):955-960
|
| [23] |
Yu L,Ye J,Zhang X. et al. Catalysis Science & Technology,2015,5(10):4830-4838
|
| [24] |
Yu L,Bai Z,Zhang X. et al. Catalysis Science & Technology,2016,6(6):1804-1809
|
| [25] |
Yu L,Li H,Zhang X. et al. Organic Letters,2014,16(5):1346-1349
|
| [26] |
Zhang X,Sun J,Ding Y. et al. Organic Letters,2015,17(23):5840-5842
|
| [27] |
Cresswell A J,Eey S T-C,Denmark S E. Nature Chemistry,2015,7(2):146-152
|
| [28] |
Trenner J, Depken C, Weber T. et al. Angewandt Chemie International Edition, 2013, 52(34):8952-8956
|
| [29] |
Deng Z,Wei J,Liao L. et al. Organic Letters,2015,17(8):1834-1837
|
| [30] |
Zhang X,Guo R,Zhao X. Organic Chemistry Frontiers,2015,2(10):1334-1337
|
| [31] |
Ortgies S,Breder A. Organic Letters,2015,17(11):2748-2751
|
| [32] |
Guo R,Huang J,Huang H. et al. Organic Letters,2016,18(3):504-507
|
| [33] |
Luo J,Zhu Z,Liu Y. et al. Organic Letters,2015,17(14):3620-3623
|
| [34] |
Chen F,Tan C K,Yeung Y-Y. Journal of the American Chemical Society,2013,135(4):1232-1235
|
|
|
|
