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烯烃不对称环氧化反应研究进展

Progress of Asymmetric Epoxidation of Olefins
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摘要 综述Salen-Mn配合物,手性酮,生物酶催化剂催化的不对称环氧化反应研究进展情况,详细介绍了酮催化剂的发展趋势。 The development of asymmetric epoxidation of olefins catalyzed by Salen - Mn complexes, chiral ketons and biologic enzymes were reviewed. The asymmetric epoxidation of olefins catalyzed by chiral ketons was explained in detail.
作者 林晓倩 卢楠
机构地区 山东师范大学化学化工与材料科学院
出处 《山东化工》 CAS 2011年第1期34-37,共4页 Shandong Chemical Industry
基金 国家基础研究资助项目(973项目 2007CB93600) 国家自然科学基金资助项目(20975064)
关键词 手性催化剂 烯烃 环氧化反应 chiral catalysts olefin asymmetric epoxidation
分类号 O621.251 [理学—有机化学]
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参考文献26

  • 1Wong O A, Shi Y. Asymmetric epoxidation of olefins catalyzed by chiral ketones and iminium salts [ J ]. Chem Rev, 2008, 108 (9): 3958-3987.
  • 2Zhang W , Leobach J L , Wilson S R , et al . Enantioselective epoxidation of unfunctionalized olefins catalyzed by salen manganese complexes [ J ] . J Am Soc , 1990, 112 (7) : 2801 -2803.
  • 3耿小兰,程丽.烯烃的不对称环氧化反应评述[J].徐州建筑职业技术学院学报,2005,5(4):17-20. 被引量：2
  • 4Murphy A, Dubois G, Stack T D P. Efficient epoxidation of electron- deficient olefins with a cationic manganese complex [J]. J Am Chem Soc, 2003, 125(18) : 5250 - 5251.
  • 5Gelalcha F G, Bitterlich B, Anilkumar G, et al. Iron - catalyzed asymmetric epoxidation of aromatic alkenes using hydrogen peroxide [ J ]. Angew Chem Int Ed, 2007, 46 (38) : 7293 -7296.
  • 6Gelalcha F G, Anilkumar G, Tse M K, et al. Biomimetie iron - catalyzed asymmetric epoxidation of aromatic alkenes by using hydrogen peroxide [J]. Chem -Eur J, 2008, 14 (25) :7687 -7698.
  • 7Marctfi - Delapierre C, Jorge - Robin A, Thibon A, et al. A new chiral diiron catalyst for enantioseletive epoxidation [J]. Chem Commum, 2007(11) :1166- 1168.
  • 8Wu Mei, Wang Bin, Wang Shoufeng, et al. Asymmetric epoxidation of oletlns with chiral bioinspired manganese complexes [J]. Org Lett, 2009, 11 (16) : 3622-3625.
  • 9Curci R, Fiorentino M, Serio M R. Asymmetric epoxidation of unfunctionalized alkenes by dioxirane intermediates generated from potassium peroxomonosulphate and chiral ketons [J]. Chem Commun,1984(3):155 -156.
  • 10Curei R , D 'Aceolti L , Fiorentino M , et al . Enantioseleetive epoxidation of unfunetionalized alkenes using dioxiranes generated in situ [ J ] . Tetrahedron Lett, 1995, 36(32) : 5831 -5834.

二级参考文献34

  • 1Smith Ⅲ A B,Walsh S P,Frohn M,et al.Diversity-oriented synthesis of polyketide natural products via iterative chemo-and stereo-selective functionlization of polyenoates:Development of a unified approach for the C(1-19) segments of lituarines A-C[J].Org Lett,2005,7(1):139-142.
  • 2Hoard D W,Moher E D,Martinelli M J,et al.Synthesis of cryptothycin 52 using the Shi epoxidation[J].Org Lett,2002,4(10):1813-1815.
  • 3McDonald F E,Bravo F,Wang X,et al.endo-Oxacyclizations of polyepoxides:biommimetic synthesis of fused polycyclic ethers[J].J Org Chem,2002,67(8):2515-2523.
  • 4Shu L,Shen Y M,Burke C,et al.An improved synthesis of a ketone catalyst for asmmetric epoxidation of olefins[J].J Org Chem,2003,68(12):4963-4965.
  • 5Morimoto Y,Nishikawa Y,Takaishi M.Total synthesis and complete assignment of the stereostructure of a cytotoxic bromotriterpene polyether (+)-aurilol[J].J Am Chem Soc,2005,127(16):5806-5807.
  • 6Halim R,Brimble M A,Merten J.Synthesis of the ABC fragment of the pectenotoxins[J].Org Lett,2005,7(13):2659-2662.
  • 7Das S,Li L S,Abraham S,et al.A bidirectional approach to the synthesis of a complete library of adjacent bis-THF annonaceous acetogenins[J].J Org Chem,2005,70(15):5922-5931.
  • 8Vidal J P,Escale R,Girard J P,et al.Lituarines A,B,and C:a new class of macrocyclic lactones from the new caledonian sea pen lituaria australasiae[J].J Org Chem,1992,57(22):5857-5860.
  • 9Robertson J,Dallimore J W P,Meo P.Synthesis of the C(1-6) and C(19-24) fragments of lituarines A,B,C[J].Org Lett,2004,6(21):3857-3859.
  • 10林国强,陈耀全,陈新滋,等.手性合成--不对称反应及其应用[M].第二版,北京:科学出版社,2001:153-205.

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山东化工
2011年 第1期

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