Stereospecific synthesis of conformationally constrained γ-amino acids: New foldamer building blocks that support helical secondary structure

Journal of the American Chemical Society

Volumn 131, Issue 44, 2009, Pages 16017-16020

  Guo, Li ^a   Chi, Yonggui ^a   Almeida, Aaron M ^a   Guzei, Ilia A ^a   Parker, Brian K ^a   Gellman, Samuel H ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID RESIDUES; BUILDING BLOCKES; FOLDAMERS; HELICAL CONFORMATION; MICHAEL ADDITIONS; OPTICALLY ACTIVE; ORGANOCATALYTIC; SECONDARY STRUCTURES; STEREOSELECTIVE SYNTHESIS; STEREOSPECIFIC SYNTHESIS;

ADDITION REACTIONS; ALDEHYDES; AMINATION; AMINO ACIDS; AMPHIPHILES; ORGANIC ACIDS; STEREOSELECTIVITY;

AMINES;

AMINO ACID DERIVATIVE; GAMMA AMINO ACID DERIVATIVE; UNCLASSIFIED DRUG; ALDEHYDE; AMINO ACID;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CRYSTAL STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MICHAEL ADDITION; PROTEIN SECONDARY STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STEREOSPECIFICITY; SUBSTITUTION REACTION; SYNTHESIS; CHEMISTRY; CONFORMATION; STEREOISOMERISM;

ALDEHYDES; AMINO ACIDS; MOLECULAR CONFORMATION; PROTEIN STRUCTURE, SECONDARY; STEREOISOMERISM;

EID: 70450162565     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja907233q     Document Type: Article

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