Constrained phenylalanyl peptides via a [2+2+2]-cycloaddition strategy

被引:67
作者
Kotha, S [1 ]
Mohanraja, K [1 ]
Durani, S [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India
关键词
D O I
10.1039/b005605g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peptide modification potentially valuable for peptidomimetic and combinatorial chemistry applications is described involving a [2+2+2]-cycloaddition reaction leading to conformationally constrained phenylalanyl peptides.
引用
收藏
页码:1909 / 1910
页数:2
相关论文
共 23 条
[1]  
[Anonymous], MODERN SYNTHETIC MET
[2]   GENERATION OF ALPHA-ACETOXYGLYCINE RESIDUES WITHIN PEPTIDE CHAINS - A NEW STRATEGY FOR THE MODIFICATION OF OLIGOPEPTIDES [J].
APITZ, G ;
JAGER, M ;
JAROCH, S ;
KRATZEL, M ;
SCHAFFELER, L ;
STEGLICH, W .
TETRAHEDRON, 1993, 49 (36) :8223-8232
[3]  
Bodanszky M., 1984, PRACTICE PEPTIDE SYN
[4]   Applications of solid-supported organic synthesis in combinatorial chemistry - Preface [J].
Bristol, JA .
TETRAHEDRON, 1997, 53 (19) :R13-R13
[5]   Stereoselective synthesis of quaternary α-amino acids.: Part 2.: Cyclic compounds [J].
Cativiela, C ;
Díaz-de-Villegas, MD .
TETRAHEDRON-ASYMMETRY, 2000, 11 (03) :645-732
[6]  
Dell CP, 1998, J CHEM SOC PERK T 1, P3873
[7]   SELECTIVE MODIFICATION OF GLYCINE RESIDUES IN DIPEPTIDES [J].
EASTON, CJ ;
SCHARFBILLIG, IM ;
TAN, EW .
TETRAHEDRON LETTERS, 1988, 29 (13) :1565-1568
[8]   PEPTIDOMIMETICS FOR RECEPTOR LIGANDS DISCOVERY, DEVELOPMENT, AND MEDICAL PERSPECTIVES [J].
GIANNIS, A .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1993, 32 (09) :1244-1267
[9]   Towards control of χ-space:: Conformationally constrained analogues of Phe, Tyr, Trp and His [J].
Gibson, SE ;
Guillo, N ;
Tozer, MJ .
TETRAHEDRON, 1999, 55 (03) :585-615
[10]   RHODIUM-CATALYZED [2+2+2]-CYCLOADDITIONS OF ACETYLENES [J].
GRIGG, R ;
SCOTT, R ;
STEVENSON, P .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (06) :1357-1364