Benziodoxole-based hypervalent iodine reagents for atom-transfer reactions

被引:269
作者
Brand, Jonathan P. [1 ]
Gonzalez, Davinia Fernandez [1 ]
Nicolai, Stefano [1 ]
Waser, Jerome [1 ]
机构
[1] EPFL SB ISIC LCSO, Ecole Polytech Fed Lausanne, BCH 4306, Lab Catalysis & Organ Synth, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
HYDROXYLATIVE PHENOL DEAROMATIZATION; MILD ELECTROPHILIC TRIFLUOROMETHYLATION; GACL3-CATALYZED ORTHO-ETHYNYLATION; CATALYZED DIRECT ALKYNYLATION; IODOXYBENZOIC ACID IBX; ORGANIC-SYNTHESIS; POLYVALENT IODINE; SYNTHETIC UTILITY; OXIDATIVE DEAROMATIZATION; TERT-BUTYLPEROXYIODANES;
D O I
10.1039/c0cc02265a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the last decades, hypervalent iodine reagents have raised from chemical curiosities to mainstream reagents in organic synthesis. The use of benziodoxole-derived reagents has been especially successful in oxidation methods, whereas non-cyclic iodinanes have been used both for oxidation and atom-transfer reactions. On the other hand, the exceptional properties of benziodoxole reagents for atom-transfer reactions have only started to attract the attention of the synthetic community more recently. In this review, progress in the use of these compounds for C-X and C-C bond formations will be presented. In particular, recent breakthroughs in trifluoromethylation and alkynylation reactions have been realized since 2006 based on benziodoxole-derived reagents and these results are the main focus of this article.
引用
收藏
页码:102 / 115
页数:14
相关论文
共 132 条
  • [81] Stoichiometric and catalytic oxidations with hypervalent organo-λ3-iodanes
    Ochiai, Masahito
    [J]. CHEMICAL RECORD, 2007, 7 (01) : 12 - 23
  • [82] Benzylic Carbon Oxidation by an in situ Formed o-Iodoxybenzoic Acid (IBX) Derivative
    Ojha, Lawanya R.
    Kudugunti, Shashi
    Maddukuri, Padma P.
    Kommareddy, Amitha
    Gunna, Meena R.
    Dokuparthi, Praveen
    Gottam, Hima B.
    Botha, Kiran K.
    Parapati, Divya R.
    Vinod, Thottumkara K.
    [J]. SYNLETT, 2009, (01) : 117 - 121
  • [83] A stabilized formulation of IBX (SIBX) for safe oxidation reactions including a new oxidative demethylation of phenolic methyl aryl ethers
    Ozanne, A
    Pouységu, L
    Depernet, D
    François, B
    Quideau, S
    [J]. ORGANIC LETTERS, 2003, 5 (16) : 2903 - 2906
  • [84] A Meta-Selective Copper-Catalyzed C-H Bond Arylation
    Phipps, Robert J.
    Gaunt, Matthew J.
    [J]. SCIENCE, 2009, 323 (5921) : 1593 - 1597
  • [85] Organocatalytic asymmetric direct α-alkynylation of cyclic β-ketoesters
    Poulsen, Thomas B.
    Bernardi, Luca
    Aleman, Jose
    Overgaard, Jacob
    Jorgensen, Karl Anker
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (02) : 441 - 449
  • [86] Total Synthesis of Wasabidienones B1 and B0 via SIBX-Mediated Hydroxylative Phenol Dearomatization
    Pouysegu, Laurent
    Marguerit, Melanie
    Gagnepain, Julien
    Lyvinec, Gildas
    Eatherton, Andrew J.
    Quideau, Stephane
    [J]. ORGANIC LETTERS, 2008, 10 (22) : 5211 - 5214
  • [87] Hypervalent iodine-mediated phenol dearomatization in natural product synthesis
    Pouysegu, Laurent
    Deffieux, Denis
    Quideau, Stephane
    [J]. TETRAHEDRON, 2010, 66 (13) : 2235 - 2261
  • [88] Oxidative dearomatization of phenols and anilines via λ3- and λ5-ilodane-mediated phenylation and oxygenation
    Quideau, S
    Pouységu, L
    Ozanne, A
    Gagnepain, J
    [J]. MOLECULES, 2005, 10 (01) : 201 - 216
  • [89] Oxidative dearomatization of phenols:: Why, how and what for?
    Quideau, Stephane
    Pouysegu, Laurent
    Deffieux, Denis
    [J]. SYNLETT, 2008, (04) : 467 - 495
  • [90] Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes and m-CPBA
    Quideau, Stephane
    Lyvinec, Gildas
    Marguerit, Melanie
    Bathany, Katell
    Ozanne-Beaudenon, Aurelie
    Buffeteau, Thierry
    Cavagnat, Dominique
    Chenede, Alain
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (25) : 4605 - 4609