Catalytic asymmetric tandem transformations triggered by conjugate additions

被引:560
作者
Guo, HC
Ma, JA [1 ]
机构
[1] Tianjin Univ, Sch Chem, Dept Chem, Tianjin 300072, Peoples R China
[2] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
关键词
asymmetric catalysis; conjugate addition; enantioselectivity; organocatalysts; tandem transformations;
D O I
10.1002/anie.200500195
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:354 / 366
页数:13
相关论文
共 126 条
[11]  
ARAI T, 1996, ANGEW CHEM, V108, P103
[12]   Catalytic enantioselective synthesis of (-)-prostaglandin E1 methyl ester based on a tandem 1,4-addition-aldol reaction [J].
Arnold, LA ;
Naasz, R ;
Minnaard, AJ ;
Feringa, BL .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (21) :7244-7254
[13]   Catalytic enantioselective synthesis of prostaglandin E1 methyl ester using a tandem 1,4-addition-aldol reaction to a cyclopenten-3,5-dione monoacetal [J].
Arnold, LA ;
Naasz, R ;
Minnaard, AJ ;
Feringa, BL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (24) :5841-5842
[14]   Catalytic enantioselective direct Michael additions of ketones to alkylidene malonates [J].
Betancort, JM ;
Sakthivel, K ;
Thayumanavan, R ;
Barbas, CF .
TETRAHEDRON LETTERS, 2001, 42 (27) :4441-4444
[15]   Enantioselective catalysis in fine chemicals production [J].
Blaser, HU .
CHEMICAL COMMUNICATIONS, 2003, (03) :293-296
[16]  
Blaser HU, 2002, ADV SYNTH CATAL, V344, P17, DOI 10.1002/1615-4169(200201)344:1<17::AID-ADSC17>3.0.CO
[17]  
2-8
[18]   Desymmetrization of enone-diones via rhodium-catalyzed diastereo- and enantioselective tandem conjugate addition-aidol cyclization [J].
Bocknack, BM ;
Wang, LC ;
Krische, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (15) :5421-5424
[19]   Industrial methods for the production of optically active intermediates [J].
Breuer, M ;
Ditrich, K ;
Habicher, T ;
Hauer, B ;
Kesseler, M ;
Stürmer, R ;
Zelinski, T .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (07) :788-824
[20]  
Breuer M., 2004, Angew. Chem, V116, P806, DOI [10.1002/ange.200300599, DOI 10.1002/ANGE.200300599]