Atropochiral C,X- and C,C-Chelating Carbon Ligands

被引:57
作者
Canac, Yves [1 ,2 ]
Chauvin, Remi [1 ,2 ]
机构
[1] CNRS, LCC, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, INP, LCC, F-31077 Toulouse, France
关键词
Atropisomerism; Atropochirality; Carbene ligands; N-heterocyclic carbenes; Metallacycles; Nitrogen heterocycles; Ylides; Asymmetric catalysis; HETEROCYCLIC CARBENE LIGANDS; OXIDATIVE KINETIC RESOLUTION; CHIRAL NHC-PD(II) COMPLEXES; PALLADIUM COMPLEXES; ASYMMETRIC HYDROGENATION; PHOSPHONIUM YLIDE; 2,2-BIS(DIPHENYLPHOSPHINO)-1,1-BINAPHTHYL BINAP; ENANTIOSELECTIVE HYDROSILYLATION; BIHETEROAROMATIC DIPHOSPHINES; ALLYLIC SUBSTITUTION;
D O I
10.1002/ejic.201000190
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the realm of atropochiral ligands initiated by the BINOL and BINAP paradigms and extended by modifications of the 1,1'-binaphthyl backbone and the coordinating heteroatoms (O, P, N, S,..), the emerging domain of the carbon versions serving as spectator ligands in catalysis is reviewed. These atropochiral C,X-chelating ligands are classified according to their coordinating mode (monodentate or bidentate), to the nature of the auxiliary donor X (a heteroatom or a carbon atom), to the overall charge of the coordinating carbon function (neutral or anionic C-ligands), and to the hapticity of the coordinating carbon function (eta(1) for NHCs and ylides, or eta(2) for alkenes). Emphasis is put on both synthetic aspects and applications in catalysis, and especially in asymmetric catalysis. This survey suggests that the "carbon ligands" should continue to provide surprises not only in coordination chemistry and in stereoselective synthesis and catalysis, but also in fundamental molecular chemistry by pushing farther the stability limits of the metal ligand interactions, thus reconciliating further the fields of organic and inorganic chemistry.
引用
收藏
页码:2325 / 2335
页数:11
相关论文
共 127 条
  • [71] New Constrained-Geometry C2-Symmetric Di-N-heterocyclic Carbene Ligands and Their Mono- and Dinuclear Rhodium(I) Complexes: Design, Synthesis, and Structural Analysis
    Lowry, Roxy J.
    Veige, Melanie K.
    Clement, Olivier
    Abboud, Khalil A.
    Ghiviriga, Ion
    Veige, Adam S.
    [J]. ORGANOMETALLICS, 2008, 27 (20) : 5184 - 5195
  • [72] Identification and characterization of a new family of catalytically highly active imidazolin-2-ylidenes
    Luan, Xinjun
    Mariz, Ronaldo
    Gatti, Michele
    Costabile, Chiara
    Poater, Albert
    Cavallo, Luigi
    Linden, Anthony
    Dorta, Reto
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (21) : 6848 - 6858
  • [73] Matching the Chirality of Monodentate N-Heterocyclic Carbene Ligands: A Case Study on Well-Defined Palladium Complexes for the Asymmetric α-Arylation of Amides
    Luan, Xinjun
    Mariz, Ronaldo
    Robert, Carine
    Gatti, Michele
    Blumentritt, Sascha
    Linden, Anthony
    Dorta, Reto
    [J]. ORGANIC LETTERS, 2008, 10 (24) : 5569 - 5572
  • [74] Catalytic Enantioselective Arylation of N-Tosylarylimines with Arylboronic Acids Using C2-Symmetric Cationic N-Heterocyclic Carbene Pd2+ Diaquo Complexes
    Ma, Guang-Ning
    Zhang, Tao
    Shi, Min
    [J]. ORGANIC LETTERS, 2009, 11 (04) : 875 - 878
  • [75] SYNTHESIS OF 2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL (BINAP), AN ATROPISOMERIC CHIRAL BIS(TRIARYL)PHOSPHINE, AND ITS USE IN THE RHODIUM(I)-CATALYZED ASYMMETRIC HYDROGENATION OF ALPHA-(ACYLAMINO)ACRYLIC ACIDS
    MIYASHITA, A
    YASUDA, A
    TAKAYA, H
    TORIUMI, K
    ITO, T
    SOUCHI, T
    NOYORI, R
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (27) : 7932 - 7934
  • [76] Nolan S P., 2006, N HETEROCYCLIC CARBE
  • [77] Asymmetric catalysis: Science and opportunities (Nobel lecture 2001)
    Noyori, R
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2003, 345 (1-2) : 15 - 32
  • [78] BINAP - AN EFFICIENT CHIRAL ELEMENT FOR ASYMMETRIC CATALYSIS
    NOYORI, R
    TAKAYA, H
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1990, 23 (10) : 345 - 350
  • [79] NOYORI R, 1994, ORG SYNTH, pCH1
  • [80] Asymmetric allylic substitution catalyzed by palladium-Yliphos complex
    Ohta, T
    Sasayama, H
    Nakajima, O
    Kurahashi, N
    Fujii, T
    Furukawa, I
    [J]. TETRAHEDRON-ASYMMETRY, 2003, 14 (05) : 537 - 542