Making carbon-nitrogen bonds in biological and chemical synthesis

被引:715
作者
Hili, Ryan [1 ]
Yudin, Andrei K. [1 ]
机构
[1] Univ Toronto, Dept Chem, Davenport Res Labs, Toronto, ON M5S 3H6, Canada
关键词
D O I
10.1038/nchembio0606-284
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The function of many biologically active molecules requires the presence of carbon-nitrogen bonds in strategic positions. The biosynthetic pathways leading to such bonds can be bypassed through chemical synthesis to synthesize natural products more efficiently and also to generate the molecular diversity unavailable in nature. © 2006 Nature Publishing Group.
引用
收藏
页码:284 / 287
页数:4
相关论文
共 20 条
  • [1] BRESLOW R, 1979, J AM CHEM SOC, V101, P1032
  • [2] Generating diverse skeletons of small molecules combinatorially
    Burke, MD
    Berger, EM
    Schreiber, SL
    [J]. SCIENCE, 2003, 302 (5645) : 613 - 618
  • [3] FUERST S, 1995, CURR MED CHEM, V1, P423
  • [4] DEUTERIUM NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY AS A PROBE OF THE STEREOCHEMISTRY OF BIOSYNTHETIC REACTIONS - THE BIOSYNTHESIS OF RETRONECINE
    GRUESORENSEN, G
    SPENSER, ID
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (25) : 7401 - 7404
  • [5] Henkel T, 1999, ANGEW CHEM INT EDIT, V38, P643, DOI 10.1002/(SICI)1521-3773(19990301)38:5<643::AID-ANIE643>3.0.CO
  • [6] 2-G
  • [7] A stereoselective synthesis of (-)-tetrodotoxin
    Hinman, A
    Du Bois, J
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (38) : 11510 - 11511
  • [8] HIGHLY ENANTIOSELECTIVE EPOXIDATION CATALYSTS DERIVED FROM 1,2-DIAMINOCYCLOHEXANE
    JACOBSEN, EN
    ZHANG, W
    MUCI, AR
    ECKER, JR
    DENG, L
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (18) : 7063 - 7064
  • [9] Kingston DGI, 2002, CURR OPIN DRUG DISC, V5, P304
  • [10] Merkx M, 2001, ANGEW CHEM INT EDIT, V40, P2782, DOI 10.1002/1521-3773(20010803)40:15<2782::AID-ANIE2782>3.0.CO