Reactivity of peptide hydroxamates: A model for the biosynthesis of β-lactam antibiotics

Tetrahedron Letters

Volumn 17, Issue 15, 1976, Pages 1137-1140

  Scott, A Ian ^a   Yoo, Sung Eun ^a   Chung, Sung Kee ^a   Lacadie, John A ^a  

^a YALE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; BETA LACTAM;

DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; INFRARED SPECTROMETRY; MASS SPECTROMETRY; METHODOLOGY; MODEL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; THEORETICAL STUDY; THIAZOLINE DERIVATIVE;

EID: 0017261276     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78000-2     Document Type: Article

References (14)

1. Incorporation of [?-2H]- and [?-3H]-L-cystine into penicillin G and the location of the label using isotope exchange and 2H nuclear magnetic resonance
2. Synthesis and reactions of ?-thioformyl dipeptides, possible biogenetic precursors of penicillin