Cyanamide in isocyanide-based MCRs

被引:26
作者
Dömling, A
Herdtweck, E
Heck, S
机构
[1] ABC Pharma, D-81243 Munich, Germany
[2] Tech Univ Munich, D-8046 Garching, Germany
关键词
MCR; Ugi reaction; cyanamide; isocyanide; combinatorial chemistry;
D O I
10.1016/j.tetlet.2006.01.032
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cyanamide reacts with enamines and isocyanides in the presence of Lewis acids to give the hitherto unknown scaffold 2-amino-(N-cyano)-amidines. Preliminary scope and limitation of this novel reaction is described. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1745 / 1747
页数:3
相关论文
共 11 条
[1]  
Bienaymé H, 2000, CHEM-EUR J, V6, P3321, DOI 10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO
[2]  
2-A
[3]   Novel and potent cyclic cyanamide-based cathepsin K inhibitors [J].
Deaton, DN ;
Hassell, AM ;
McFadyen, RB ;
Miller, AB ;
Miller, LR ;
Shewchuk, LM ;
Tavares, FX ;
Willard, DH ;
Wright, LL .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (07) :1815-1819
[4]   Recent developments in isocyanide based multicomponent reactions in applied chemistry [J].
Dömling, A .
CHEMICAL REVIEWS, 2006, 106 (01) :17-89
[5]  
Dömling A, 2000, ANGEW CHEM INT EDIT, V39, P3168, DOI 10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO
[6]  
2-U
[7]  
Hulme C, 2003, CURR OPIN DRUG DISC, V6, P921
[8]   Novel α-amino amidine synthesis via scandium(III) triflate mediated 3CC Ugi condensation reaction [J].
Keung, W ;
Bakir, F ;
Patron, AP ;
Rogers, D ;
Priest, CD ;
Darmohusodo, V .
TETRAHEDRON LETTERS, 2004, 45 (04) :733-737
[9]  
Lockhoff O, 2002, COMB CHEM HIGH T SCR, V5, P361
[10]   Recent advances in solution-phase multicomponent methodology for the synthesis of heterocyclic compounds [J].
Orru, RVA ;
de Greef, M .
SYNTHESIS-STUTTGART, 2003, (10) :1471-1499