Recent advances in isocyanide-based multicomponent chemistry

被引:515
作者
Dömling, A [1 ]
机构
[1] Morphochem AG, D-81379 Munich, Germany
关键词
D O I
10.1016/S1367-5931(02)00328-9
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
Multicomponent reactions (MCRs) provide a powerful tool towards the one-pot synthesis of diverse and complex compounds on the one hand and small and 'drug-like' heterocycles on the other hand. No other single synthesis technology enables chemists to search such large chemical spaces as provided by MCRs. MCRs that involve isocyanides are by far the most versatile reactions in terms of scaffolds and number of accessible compounds.
引用
收藏
页码:306 / 313
页数:8
相关论文
共 23 条
[1]   Passerini multicomponent reaction of protected α-aminoaldehydes as a tool for combinatorial synthesis of enzyme inhibitors [J].
Banfi, L ;
Guanti, G ;
Riva, R .
CHEMICAL COMMUNICATIONS, 2000, (11) :985-986
[2]  
Barton D. H. R., 1990, Aldrichimica Acta, V23, P3
[3]   A novel three-component butenolide synthesis [J].
Beck, B ;
Magnin-Lachaux, M ;
Herdtweck, E ;
Dömling, A .
ORGANIC LETTERS, 2001, 3 (18) :2875-2878
[4]  
Corey E. J., 1995, LOGIC CHEM SYNTHESIS
[5]   THE 7-COMPONENT REACTION [J].
DOMLING, A ;
UGI, I .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (04) :563-564
[6]   The discovery of new isocyanide-based multi-component reactions [J].
Dömling, A .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (03) :318-323
[7]  
Heck S, 2000, SYNLETT, P424
[8]   An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction [J].
Kim, YB ;
Choi, EH ;
Keum, G ;
Kang, SB ;
Lee, DH ;
Koh, HY ;
Kim, YS .
ORGANIC LETTERS, 2001, 3 (26) :4149-4152
[9]   Pairwise use of complexity-generating reactions in diversity-oriented organic synthesis [J].
Lee, DS ;
Sello, JK ;
Schreiber, SL .
ORGANIC LETTERS, 2000, 2 (05) :709-712
[10]  
Nair V, 2001, CHEM LETT, P738