Construction of peptoids with all trans -amide backbones and peptoid reverse turns via the tactical incorporation of N -aryl side chains capable of hydrogen bonding

Journal of Organic Chemistry

Volumn 75, Issue 18, 2010, Pages 6068-6078

  Stringer, Joseph R ^a   Crapster, J Aaron ^a   Guzei, Ilia A ^a   Blackwell, Helen E ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2D-NMR SPECTROSCOPY; CONFORMATIONAL PREFERENCES; DIHEDRAL ANGLES; FOLDAMERS; HYDROGEN BOND DONORS; HYDROGEN BONDINGS; MODEL SYSTEM; NATURAL BIOPOLYMERS; NON-COVALENT INTERACTION; PEPTOIDS; RATIONAL DESIGN; SECONDARY AND TERTIARY STRUCTURES; SIDE CHAINS; SOLID-PHASE; STEREOELECTRONIC INTERACTIONS; STRUCTURAL MOTIFS; SYNTHESIS METHODOLOGY; TURN STRUCTURE;

AMIDES; BIOMIMETICS; BIOPOLYMERS; CONFORMATIONS; HYDROGEN; MONOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLIGOMERS; STRUCTURAL DESIGN; X RAY CRYSTALLOGRAPHY;

HYDROGEN BONDS;

MONOMER; OLIGOMER; PEPTOID;

ARTICLE; BIOMIMETICS; DRUG DESIGN; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGEN BOND; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; X RAY CRYSTALLOGRAPHY;

AMIDES; CRYSTALLOGRAPHY, X-RAY; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PEPTOIDS; STEREOISOMERISM;

EID: 77956552715     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101075a     Document Type: Article

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