Diastereomeric fluoroolefins as peptide bond mimics prepared by asymmetric reductive amination of α-fluoroenones

Angewandte Chemie - International Edition

Volumn 46, Issue 8, 2007, Pages 1290-1292

  Dutheuil, Guillaume ^a   Couve Bonnaire, Samuel ^a   Pannecoucke, Xavier ^a  

^a IRCOF   (France)

Author keywords

Asymmetric synthesis; Fluoroenones; Fluoroolefins; Peptidomimetics; Reductive amination

Indexed keywords

AMINATION; CHEMICAL BONDS; PEPTIDES; STEREOCHEMISTRY;

ASYMMETRIC SYNTHESIS; FLUOROENONES; FLUOROOLEFINS; PEPTIDOMIMETICS; REDUCTIVE AMINATION;

OLEFINS;

ALKENE; AMIDE; BIOMIMETIC MATERIAL; FLUORINE; KETONE; PEPTIDE;

AMINATION; ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALKENES; AMIDES; AMINATION; BIOMIMETIC MATERIALS; FLUORINE; KETONES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; PEPTIDES; STEREOISOMERISM;

EID: 34047235610     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604246     Document Type: Article

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