A facile Pd(0)-catalyzed regio- and stereoselective diamination of conjugated dienes and trienes

被引:218
作者
Du, Haifeng [1 ]
Zhao, Baoguo [1 ]
Shi, Yian [1 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
关键词
D O I
10.1021/ja0680562
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper describes a novel diamination process using di-t-butyldiaziridinone as the nitrogen source and Pd(PPh3)(4) as catalyst. A wide variety of conjugated dienes and trienes can be effectively diaminated in good yields with high regio- and stereoselectivities in short reaction time.
引用
收藏
页码:762 / 763
页数:2
相关论文
共 32 条
  • [11] Hassner A., 1983, CHEM HETEROCYCLIC CO, P547
  • [12] PALLADIUM(II)-ASSISTED REACTIONS OF MONOOLEFINS
    HEGEDUS, LS
    [J]. TETRAHEDRON, 1984, 40 (13) : 2415 - 2434
  • [13] FIRM EVIDENCE FOR CIS-AMINOPALLADATION IN THE REACTION OF 1-AMINOHEXATRIENES WITH PALLADIUM DICHLORIDE
    ISOMURA, K
    OKADA, N
    SARUWATARI, M
    YAMASAKI, H
    TANIGUCHI, H
    [J]. CHEMISTRY LETTERS, 1985, (03) : 385 - 388
  • [14] Novel synthesis of diazetidine-2,4-dione by ring expansion of diaziridinone
    Komatsu, M
    Tamabuchi, S
    Minakata, S
    Ohshiro, Y
    [J]. HETEROCYCLES, 1999, 50 (01) : 67 - 70
  • [15] Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry
    Kotti, SRSS
    Timmons, C
    Li, GG
    [J]. CHEMICAL BIOLOGY & DRUG DESIGN, 2006, 67 (02) : 101 - 114
  • [16] Li GG, 2001, ANGEW CHEM INT EDIT, V40, P4277, DOI 10.1002/1521-3773(20011119)40:22<4277::AID-ANIE4277>3.0.CO
  • [17] 2-I
  • [18] α,β-Differentiated tandem diamination of cinnamic esters using N,N-dichloro-2-nitrobenzenesulfonamide and acetonitrile as the nitrogen sources
    Li, GG
    Kim, SH
    Wei, HX
    [J]. TETRAHEDRON LETTERS, 2000, 41 (45) : 8699 - 8703
  • [19] LIU G, 2003, J AM CHEM SOC, V128, P7179
  • [20] Lucet D, 1998, ANGEW CHEM INT EDIT, V37, P2581, DOI 10.1002/(SICI)1521-3773(19981016)37:19<2580::AID-ANIE2580>3.0.CO