An unusual type of ruthenium-catalyzed transfer hydrogenation of ketones with alcohols accompanied by C-C coupling

被引:185
作者
Cho, CS [1 ]
Kim, BT [1 ]
Kim, TJ [1 ]
Shim, SC [1 ]
机构
[1] Kyungpook Natl Univ, Coll Engn, Dept Ind Chem, Taegu 702701, South Korea
关键词
D O I
10.1021/jo0108459
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:9020 / 9022
页数:3
相关论文
共 30 条
  • [1] [Anonymous], 1996, REDUCTIONS ORGANIC C
  • [2] Backball J.-E., 1992, PERSPECTIVES COORDIN, P463
  • [3] BENNET MA, 1984, COMPREHENSIVE ORGANO, V4, P945
  • [4] DISPROPORTIONATION OF ACYCLIC KETONES TO CARBOXYLATE IONS AND ETHERS - A POISONING REACTION ON THE WAY TO THE CHEMOSELECTIVE REDUCTION OF ALPHA,BETA-UNSATURATED KETONES TO ALLYLIC ALCOHOLS VIA HYDROGEN-TRANSFER CATALYZED BY A NONCLASSICAL RUTHENIUM(II) TRIHYDRIDE
    BIANCHINI, C
    FARNETTI, E
    FREDIANI, P
    GRAZIANI, M
    PERUZZINI, M
    POLO, A
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1991, (19) : 1336 - 1337
  • [5] BLUM J, 1972, TETRAHEDRON LETT, P1015
  • [6] CATALYTIC TRANSFER HYDROGENATION
    BRIEGER, G
    NESTRICK, TJ
    [J]. CHEMICAL REVIEWS, 1974, 74 (05) : 567 - 580
  • [7] ASYMMETRIC CATALYZES .31. ENANTIOSELECTIVE CATALYTIC REDUCTION OF DEHYDRO AMINO-ACIDS WITH FORMIC-ACID
    BRUNNER, H
    KUNZ, M
    [J]. CHEMISCHE BERICHTE-RECUEIL, 1986, 119 (09): : 2868 - 2873
  • [8] Synthesis of quinolines via ruthenium-catalysed amine exchange reaction between anilines and trialkylamines
    Cho, CS
    Oh, BH
    Kim, JS
    Kim, TJ
    Shim, SC
    [J]. CHEMICAL COMMUNICATIONS, 2000, (19) : 1885 - 1886
  • [9] Ruthenium-catalyzed heteroannulation of anilines with alkanolammonium chlorides leading to indoles
    Cho, CS
    Kim, JH
    Kim, TJ
    Shim, SC
    [J]. TETRAHEDRON, 2001, 57 (16) : 3321 - 3329
  • [10] Ruthenium-catalysed synthesis of indoles from anilines and trialkanolamines in the presence of tin(II) chloride dihydrate
    Cho, CS
    Lim, HK
    Shim, SC
    Kim, TJ
    Choi, HJ
    [J]. CHEMICAL COMMUNICATIONS, 1998, (09) : 995 - 996