Reactivity of 1-aminoazetidine-2-carboxylic acid during peptide forming procedures: Observation of an unusual variant of the hydrazino turn

Tetrahedron Letters

Volumn 54, Issue 8, 2013, Pages 802-805

  Altmayer Henzien, Amandine ^a   Declerck, Valérie ^a   Guillot, Régis ^a   Aitken, David J ^a  

^a UNIVERSITÉ PARIS SACLAY   (France)

Author keywords

Azetidine; Hydrazino acid; Hydrazino turn; Hydrogen bonding; Peptides; Ring opening reaction

Indexed keywords

1 AMINOAZETIDINE 2 CARBOXYLIC ACID; CARBOXYLIC ACID DERIVATIVE; DIPEPTIDE; HYDRAZINE; PEPTIDE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CRYSTAL STRUCTURE; DIASTEREOISOMER; HYDROGEN BOND; MOLECULAR DYNAMICS; PROTEIN CONFORMATION; RING OPENING; X RAY DIFFRACTION;

EQUIDAE;

EID: 84872303177     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.11.112     Document Type: Article

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