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
  • [21] Functionalized 2-azabicyclo[3.3.0]octanes as ligands in the enantioselective catalysis
    Aurich, HG
    Soeberdt, M
    [J]. TETRAHEDRON LETTERS, 1998, 39 (17) : 2553 - 2554
  • [22] Catalytic conjugate addition promoted by the copper(I)-monothiobinaphthol system .2. Optimal ligand synthesis and initial catalytic results
    Azad, SM
    Bennett, SMW
    Brown, SM
    Green, J
    Sinn, E
    Topping, CM
    Woodward, S
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (05): : 687 - 694
  • [23] New recoverable poly(ethylene glycol)-supported C1-diamino-oligothiophene ligands for palladium-promoted asymmetric allylic alkylation (AAA) reactions
    Bandini, Marco
    Benaglia, Maurizio
    Quinto, Tommaso
    Tommasi, Simona
    Umani-Ronchi, Achille
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (12-13) : 1521 - 1527
  • [24] Chiral P,S-ligands based on beta-d-thioglucose tetraacetate. Palladium(II) complexes and allylic alkylation
    Barbaro, P
    Currao, A
    Herrmann, J
    Nesper, R
    Pregosin, PS
    Salzmann, R
    [J]. ORGANOMETALLICS, 1996, 15 (07) : 1879 - 1888
  • [25] Homogeneous catalysis with transition metal complexes containing sulfur ligands
    Bayón, JC
    Claver, C
    Masdeu-Bultó, AM
    [J]. COORDINATION CHEMISTRY REVIEWS, 1999, 193-5 : 73 - 145
  • [26] Steric and electronic tuning of chiral bis(oxazoline) ligands with 3,3'-bithiophene backbone
    Benaglia, M
    Benincori, T
    Mussini, P
    Pilati, T
    Rizzo, S
    Sannicolò, F
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (19) : 7488 - 7495
  • [27] (DIPHENYLPHOSPHINO)-BIHETEROARYLS - THE FIRST EXAMPLE OF A NEW CLASS OF CHIRAL ATROPISOMERIC CHELATING DIPHOSPHINE LIGANDS FOR TRANSITION-METAL-CATALYZED STEREOSELECTIVE REACTIONS
    BENINCORI, T
    BRENNA, E
    SANNICOLO, F
    TRIMARCO, L
    ANTOGNAZZA, P
    CESAROTTI, E
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (06) : 685 - 686
  • [28] 2,5-dimethyl-3,4-bis[(2R,5R)-2,5-dimethylphospholano]thiophene:: First member of the hetero-DuPHOS family
    Benincori, T
    Pilati, T
    Rizzo, S
    Sannicolò, F
    Burk, MJ
    de Ferra, L
    Ullucci, E
    Piccolo, O
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (14) : 5436 - 5441
  • [29] 2,2′,5,5′-tetramethyl-4,4′-bis(diphenylphoshino)-3,3′-bithiophene:: A new, very efficient, easily accessible, chiral biheteroaromatic ligand for homogeneous stereoselective catalysis
    Benincori, T
    Cesarotti, E
    Piccolo, O
    Sannicolò, F
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (07) : 2043 - 2047
  • [30] A new modular class of easily accessible, inexpensive, and efficient chiral diphosphine ligands for homogeneous stereoselective catalysis
    Benincori, T
    Gladiali, S
    Rizzo, S
    Sannicolò, F
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (17) : 5940 - 5942