Regioselective synthesis of antiparallel loops on a macrocyclic scaffold constrained by oxazoles and thiazoles


Autoria(s): Singh, Y; Stoermer, MJ; Lucke, AJ; Glenn, MP; Fairlie, DP
Data(s)

01/01/2002

Resumo

[GRAPHICS] The regioselective syntheses and structures are reported for two tris-macrocylic compounds, each possessing two antiparallel loops on a macrocyclic scaffold constrained by two oxazoles and two thiazoles. NMR solution structures show the loops projecting from the same face of the macrocycle. Such molecules are shown to be prototypes for mimicking multiple loops of proteins.

Identificador

http://espace.library.uq.edu.au/view/UQ:64146

Idioma(s)

eng

Publicador

American Chemical Society

Palavras-Chave #Chemistry, Organic #Cyclic-peptides #Marine Cyclopeptides #Natural-products #Amino-acids #Conformations #Tunicate #Mimetics #Template #Antibody #Cyclooligomerization #C1 #250302 Biological and Medical Chemistry #780103 Chemical sciences
Tipo

Journal Article