An Efficient Procedure for Palladium-Catalyzed Reduction of Aryl/Enol Triflates

被引:0
|
作者
Kotsuki, H.
Datta, P. K.
Hayakawa, H.
Suenaga, H.
机构
来源
Synthesis | / 11期
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [41] PALLADIUM-CATALYZED OLEFINATION OF VINYL TRIFLATES
    SCOTT, WJ
    PENA, MR
    SWARD, K
    STOESSEL, SJ
    STILLE, JK
    JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (13): : 2302 - 2308
  • [42] PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS OF VINYL AND ARYL TRIFLATES WITH TETRAARYLBORATES
    CIATTINI, PG
    MORERA, E
    ORTAR, G
    TETRAHEDRON LETTERS, 1992, 33 (33) : 4815 - 4818
  • [43] PALLADIUM-CATALYZED PHOSPHORYLATION OF ALKENYL TRIFLATES
    HOLT, DA
    ERB, JM
    TETRAHEDRON LETTERS, 1989, 30 (40) : 5393 - 5396
  • [44] PALLADIUM-CATALYZED BETA-ARYLATION OF MODIFIED VINYL ETHERS WITH ARYL TRIFLATES
    BADONE, D
    GUZZI, U
    TETRAHEDRON LETTERS, 1993, 34 (22) : 3603 - 3606
  • [45] Palladium-catalyzed Substitution of Ketone or Aldehyde Bearing Aryl Triflates by Amines or Amides
    Tao Xiaochun
    Dai Chunya
    Cao Xiongjie
    Cai Lisheng
    Pike, Victor W.
    CHINESE JOURNAL OF CHEMISTRY, 2009, 27 (02) : 403 - 407
  • [46] Palladium-catalyzed cross-coupling reaction of cyclopropylboronic acids with aryl triflates
    Yao, ML
    Deng, MZ
    SYNTHESIS-STUTTGART, 2000, (08): : 1095 - 1100
  • [47] Solvent-free palladium-catalyzed phosphination of aryl bromides and triflates with triphenylphosphine
    Kwong, FY
    Lai, CW
    Chan, KS
    TETRAHEDRON LETTERS, 2002, 43 (19) : 3537 - 3539
  • [48] Palladium-catalyzed enantioselective carbonylative cyclization of aryl and alkenyl triflates with carbon monoxide
    Hayashi, T
    Tang, J
    Kato, K
    ORGANIC LETTERS, 1999, 1 (09) : 1487 - 1489
  • [49] Mild Palladium-Catalyzed Cyanation of (Hetero)aryl Halides and Triflates in Aqueous Media
    Cohen, Daniel T.
    Buchwald, Stephen L.
    ORGANIC LETTERS, 2015, 17 (02) : 202 - 205
  • [50] Visible-Light-Induced Palladium-Catalyzed Generation of Aryl Radicals from Aryl Triflates
    Ratushnyy, Maxim
    Kvasovs, Nikita
    Sarkar, Sumon
    Gevorgyan, Vladimir
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (26) : 10316 - 10320