A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols

被引:657
作者
Fernández-Rodríguez, MA [1 ]
Shen, QL [1 ]
Hartwig, JF [1 ]
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
D O I
10.1021/ja0580340
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general catalytic system for the coupling of aryl halides and sulfonates with thiols based on the use of the CyPF-t-Bu ligand (1) is reported. The reactions catalyzed by complexes of 1 occur in excellent yields with broad scope and exhibit extraordinary turnover numbers and high tolerance of functional groups. Turnover numbers usually exceed those of previous catalysts by 2 or 3 orders of magnitude. In addition, the reactions of aryl tosylates with alkane thiols to form aryl sulfides are reported for the first time. Finally, the synthesis of a diarylsulfide from two bromoarenes was accomplished using a hydrogen sulfide surrogate. Copyright © 2006 American Chemical Society.
引用
收藏
页码:2180 / 2181
页数:2
相关论文
共 28 条
  • [1] Efficient syntheses of AZD4407 via thioether formation by nucleophilic attack of organometallic species on sulphur
    Alcaraz, ML
    Atkinson, S
    Cornwall, P
    Foster, AC
    Gill, DM
    Humphries, LA
    Keegan, PS
    Kemp, R
    Merifield, E
    Nixon, RA
    Noble, AJ
    O'Beirne, D
    Patel, ZM
    Perkins, J
    Rowan, P
    Sadler, P
    Singleton, JT
    Tornos, J
    Watts, AJ
    Woodland, IA
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2005, 9 (05) : 555 - 569
  • [2] [Anonymous], 2002, HDB ORGANOPALLADIUM
  • [3] CARBON-HETEROATOM BOND-FORMING REDUCTIVE ELIMINATION - MECHANISM, IMPORTANCE OF TRAPPING REAGENTS, AND UNUSUAL ELECTRONIC EFFECTS DURING FORMATION OF ARYL SULFIDES
    BARANANO, D
    HARTWIG, JF
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (10) : 2937 - 2938
  • [4] CRISTAU HJ, 1981, SYNTHESIS-STUTTGART, P892
  • [5] CuI-catalyzed coupling reactions of aryl iodides and bromides with thiols promoted by amino acid ligands
    Deng, W
    Zou, Y
    Wang, YF
    Liu, L
    Guo, QX
    [J]. SYNLETT, 2004, (07) : 1254 - 1258
  • [6] Sterically hindered chelating alkyl phosphines provide large rate accelerations in palladium-catalyzed amination of aryl iodides, bromides, and chlorides, and the first amination of aryl tosylates
    Hamann, BC
    Hartwig, JF
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (29) : 7369 - 7370
  • [7] HARTWIG JF, 2002, MODERN ARENE CHEM, P107
  • [8] A general palladium-catalyzed coupling of aryl bromides/triflates and thiols
    Itoh, T
    Mase, T
    [J]. ORGANIC LETTERS, 2004, 6 (24) : 4587 - 4590
  • [9] Metal-catalyzed carbon-sulfur bond formation
    Kondo, T
    Mitsudo, T
    [J]. CHEMICAL REVIEWS, 2000, 100 (08) : 3205 - 3220
  • [10] REACTIONS OF ARYL HALIDES WITH THIOLATE ANIONS IN PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM PREPARATION OF ARYL SULFIDES
    KOSUGI, M
    SHIMIZU, T
    MIGITA, T
    [J]. CHEMISTRY LETTERS, 1978, (01) : 13 - 14