TY  -  
T1  - Structural Diversity of Peptoids : Tube-Like Structures of Macrocycles 
SN  -  /  
UR  - http://hdl.handle.net/10138/325433 
T3  -  
A1  - Herlan, Claudine Nicole; Sommer, Katharina; Weis, Patrick; Nieger, Martin; Bräse, Stefan 
A2  -  
PB  -  
Y1  - 2021 
LA  - eng 
AB  - Peptoids, or poly-N-substituted glycines, are characterised by broad structural diversity. Compared to peptides, they are less restricted in rotation and lack backbone-derived H bonding. Nevertheless, certain side chains force the peptoid backbone into distinct conformations. Designable secondary structures like helices or nanosheets arise from this knowledge. Herein, we report the copper-catalysed alkyne-azide cycloaddition (CuAAC) of macrocycles to form innovative tube-like tricyclic peptoids,... 
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IS  -  
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OP  -  
KW  - peptidomimetics; tricyclic peptoids; CuAAC; foldamers; NANOSHEETS; OLIGOMERS; PEPTIDES; HELICES; WATER; PEPTIDOMIMETICS; GLYCINES); POLYMERS; ORDER; 116 Chemical sciences 
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ER  -