Asymmetric catalytic aza-Henry reactions leading to 1,2-diamines and 1-,2-diaminocarboxylic acids

被引:193
作者
Westermann, B [1 ]
机构
[1] Univ Gesamthsch Paderborn, Fac Nat Sci, D-33095 Paderborn, Germany
关键词
asymmetric syntheses; aza-Henry reactions; diamines; Lewis acids; Mannich reactions;
D O I
10.1002/anie.200390071
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the wake of the aldol and Mannich reactions, textbook examples of asymmetric reactions, comes the aza-Henry reaction (aka nitro-Mannich reaction), which leads to 1,2-diamines or α,β-diaminocarboxylic acids (see scheme, PG= protecting group). Recent developments point to a bright future for this transformation.
引用
收藏
页码:151 / 153
页数:3
相关论文
共 31 条
[1]   The nitro-Mannich reaction and its application to the stereoselective synthesis of 1,2-diamines [J].
Adams, H ;
Anderson, JC ;
Peace, S ;
Pennell, AMK .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (26) :9932-9934
[2]  
Anderson JC, 2000, SYNLETT, P850
[3]  
[Anonymous], 2001, ANGEW CHEM
[4]  
BACKVALL JE, 1975, TETRAHEDRON LETT, P2225
[5]  
BACKVALL JE, 1978, TETRAHEDRON LETT, P163
[6]  
Bolm C., 2000, Catal. Asymmetric Synth, V2nd, P399
[7]   Copper-catalyzed enantioselective Henry reactions of α-keto esters:: An easy entry to optically active β-nitro-α-hydroxy esters and β-amino-α-hydroxy esters [J].
Christensen, C ;
Juhl, K ;
Hazell, RG ;
Jorgensen, KA .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (14) :4875-4881
[8]  
Christoffers J, 2001, ANGEW CHEM INT EDIT, V40, P4591, DOI 10.1002/1521-3773(20011217)40:24<4591::AID-ANIE4591>3.0.CO
[9]  
2-V
[10]  
Christoffers J., 2001, ANGEW CHEM, V113, P4725, DOI DOI 10.1002/1521-3757(20011217)113:24