Chiral sulfur ligands for asymmetric catalysis

被引:539
作者
Mellah, Mohamed [1 ]
Voituriez, Arnaud [1 ]
Schulz, Emmanuelle [1 ]
机构
[1] Univ Paris Sud, UMR 8182, ICMMO, F-91405 Orsay, France
关键词
D O I
10.1021/cr068440h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Around 350 references dealing with the use of chiral sulfur ligands for asymmetric catalysis. These reports are clear indication for the efficient use of such ligands promoting numerous catalytic transformations. Their preparation arose from the search for synthetically easily available compounds that were relatively easy to handle and store. Their study is more recent compared to that of P- or N- ligands, although their efficiency for promoting symmetrical catalysis is less impressive. However, they overtake other ligands in terms of activity and enantioselectivity. Additionally, due to their versatility, S,N ligands have a promising future for promoting, especially, C-C bond formations. Due to their stability, the asymmetric heterogenous catalysis is a good way of developing these ligands in an economic and environmentally friendly manner.
引用
收藏
页码:5133 / 5209
页数:77
相关论文
共 350 条
  • [1] THE STEREODYNAMICS OF METAL-COMPLEXES OF SULFUR-CONTAINING, SELENIUM-CONTAINING, AND TELLURIUM-CONTAINING LIGANDS
    ABEL, EW
    BHARGAVA, SK
    ORRELL, KG
    [J]. PROGRESS IN INORGANIC CHEMISTRY, 1984, 32 : 1 - 118
  • [2] NUCLEAR-MAGNETIC-RESONANCE INVESTIGATIONS OF A NOVEL INTRAMOLECULAR METHYLTHIO REPLACEMENT PROCESS IN PALLADIUM(II) AND PLATINUM(II) COMPLEXES OF MIXED SULFUR PHOSPHINE-LIGANDS
    ABEL, EW
    DORMER, JC
    ELLIS, D
    ORRELL, KG
    SIK, V
    HURSTHOUSE, MB
    MAZID, MA
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1992, (06): : 1073 - 1080
  • [3] Chiral thiazoline ligands: application in Pd-catalysed allylic substitution
    Abrunhosa, I
    Delain-Bioton, L
    Gaumont, AC
    Gulea, M
    Masson, S
    [J]. TETRAHEDRON, 2004, 60 (41) : 9263 - 9272
  • [4] Synthesis of new chiral thiazoline-containing ligands
    Abrunhosa, I
    Gulea, M
    Levillain, J
    Masson, S
    [J]. TETRAHEDRON-ASYMMETRY, 2001, 12 (20) : 2851 - 2859
  • [5] Adams E, 1999, J ORG CHEM, V64, P8256
  • [6] Catalytic cyclopropanation of electron deficient alkenes mediated by chiral and achiral sulfides: scope and limitations in reactions involving phenyldiazomethane and ethyl diazoacetate
    Aggarwal, VK
    Smith, HW
    Hynd, G
    Jones, RVH
    Fieldhouse, R
    Spey, SE
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (19): : 3267 - 3276
  • [7] Controlling stereochemical outcomes of asymmetric processes by catalyst remote molecular functionalizations: Chiral diamino-oligothiophenes (DATs) as ligands in asymmetric catalysis
    Albano, VG
    Bandini, M
    Barbarella, G
    Melucci, M
    Monari, M
    Piccinelli, F
    Tommasi, S
    Umani-Ronchi, A
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (03) : 667 - 675
  • [8] Novel chiral diamino-oligothiophenes as valuable ligands in Pd-catalyzed allylic alkylations. On the "primary" role of "secondary" interactions in asymmetric catalysis
    Albano, VG
    Bandini, M
    Melucci, M
    Monari, M
    Piccinelli, F
    Tommasi, S
    Umani-Ronchi, A
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2005, 347 (11-13) : 1507 - 1512
  • [9] A new P,S-Chiral auxiliary derived from thioglucose. X-ray structure of a palladium 1,3-diphenylallyl complex with a strongly rotated allyl ligand
    Albinati, A
    Pregosin, PS
    Wick, K
    [J]. ORGANOMETALLICS, 1996, 15 (10) : 2419 - 2421
  • [10] Synthesis of an octahydro-1,1′-binaphthyl thioether ligand and comparison with unhydrogenated binaphthyl analogues
    Albrow, V
    Biswas, K
    Crane, A
    Chaplin, N
    Easun, T
    Gladiali, S
    Lygo, B
    Woodward, S
    [J]. TETRAHEDRON-ASYMMETRY, 2003, 14 (18) : 2813 - 2819