Transition-metal-catalyzed reactions in heterocyclic synthesis

被引:1556
作者
Nakamura, I [1 ]
Yamamoto, Y [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai, Miyagi 9808578, Japan
关键词
D O I
10.1021/cr020095i
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterocycles are especially important in chemical and pharmaceutical industries. It seems that industrial people have been using mostly the traditional and conventional transformations for the synthesis of heterocycles, perhaps because those reactions are reliable and robust and proceed generally at low cost. However, it is also true that some of those reactions are accompanied with waste byproducts. In this sense, transition-metal-catalyzed reactions minimize such waste and are in general environmentally friendly. Heterocycles having a complicated structure with many labile functional groups can be synthesized often from rather simple starting materials through sequential catalytic processes.
引用
收藏
页码:2127 / 2198
页数:72
相关论文
共 868 条
[1]   A new approach to the synthesis of functionalized pyrido[2,3-b]lindoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C-9a positions [J].
Abouabdellah, A ;
Dodd, RH .
TETRAHEDRON LETTERS, 1998, 39 (15) :2119-2122
[2]   A highly reactive titanium precatalyst for intramolecular hydroamination reactions [J].
Ackermann, L ;
Bergman, RG .
ORGANIC LETTERS, 2002, 4 (09) :1475-1478
[3]  
Ackermann L, 2001, SYNLETT, P397
[4]  
Aeilts SL, 2001, ANGEW CHEM INT EDIT, V40, P1452, DOI 10.1002/1521-3773(20010417)40:8<1452::AID-ANIE1452>3.0.CO
[5]  
2-G
[6]   A convenient method for the efficient removal of ruthenium byproducts generated during olefin metathesis reactions [J].
Ahn, YM ;
Yang, K ;
Georg, GI .
ORGANIC LETTERS, 2001, 3 (09) :1411-1413
[7]   Synthesis of a tricyclic mescaline analogue by catalytic C-H bond activation [J].
Ahrendt, KA ;
Bergman, RG ;
Ellman, JA .
ORGANIC LETTERS, 2003, 5 (08) :1301-1303
[8]   Synthesis of cyclic RGD derivatives via solid phase macrocyclization using the Heck reaction [J].
Akaji, K ;
Teruya, K ;
Akaji, M ;
Aimoto, S .
TETRAHEDRON, 2001, 57 (12) :2293-2303
[9]   Cu(I)-catalyzed enantioselective [2+2] cycloaddition of 1-methoxyallenylsilane with α-imino ester:: Chiral synthesis of α,β-unsaturated acylsilanes [J].
Akiyama, T ;
Daidouji, K ;
Fuchibe, K .
ORGANIC LETTERS, 2003, 5 (20) :3691-3693
[10]   Rh(I)-catalyzed coupling cyclization of N-aryl trifluoroacetimidoyl chlorides with alkynes:: One-pot synthesis of fluorinated quinolines [J].
Amii, H ;
Kishikawa, Y ;
Uneyama, K .
ORGANIC LETTERS, 2001, 3 (08) :1109-1112