High-throughput methods for the development of new catalytic asymmetric reactions

被引:60
作者
Traverse, JF [1 ]
Snapper, ML [1 ]
机构
[1] Boston Coll, Dept Chem, Eugene F Merkert Chem Ctr, Chestnut Hill, MA 02467 USA
关键词
D O I
10.1016/S1359-6446(02)02436-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chiral, single enantiomer pharmaceuticals have become increasingly more important. Therefore, research aimed at providing new methods for their selective preparation has taken on an even greater importance. One of the most efficient strategies for the synthesis of non-racemic, chiral molecules is asymmetric catalysis. There are many variables involved in the discovery of a new catalytic asymmetric transformation; hence, methods for the rapid screening of large numbers of catalysts have been developed. Herein, these techniques and strategies for the rapid discovery of novel asymmetric catalysts are reviewed.
引用
收藏
页码:1002 / 1012
页数:11
相关论文
共 77 条
  • [71] Thermographic selection of effective catalysts from an encoded polymer-bound library
    Taylor, SJ
    Morken, JP
    [J]. SCIENCE, 1998, 280 (5361) : 267 - 270
  • [72] Tsukamoto M, 2002, ADV SYNTH CATAL, V344, P453, DOI 10.1002/1615-4169(200207)344:5<453::AID-ADSC453>3.0.CO
  • [73] 2-U
  • [74] van Delden RA, 2001, ANGEW CHEM INT EDIT, V40, P3198, DOI 10.1002/1521-3773(20010903)40:17<3198::AID-ANIE3198>3.0.CO
  • [75] 2-I
  • [76] Novel methods for biocatalyst screening
    Wahler, D
    Reymond, JL
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (02) : 152 - 158
  • [77] Complete reversal of enantioselectivity of an enzyme-catalyzed reaction by directed evolution
    Zha, DX
    Wilensek, S
    Hermes, M
    Jaeger, KE
    Reetz, MT
    [J]. CHEMICAL COMMUNICATIONS, 2001, (24) : 2664 - 2665