A concise synthesis of penems

Tetrahedron Letters

Volumn 31, Issue 30, 1990, Pages 4359-4362

  Barker, A J ^a   Campbell, M M ^b   Jenkins, M J ^a  

^a AKZO NOBEL CENTRAL RESEARCH   (Netherlands)

^b UNIVERSITY OF BATH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PENEM DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; METHODOLOGY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL;

EID: 0025334140     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97622-6     Document Type: Article

References (21)

1. HRE 664, a new parenteral penem. I. Antibacterial activity in vitro.
2. Stereoselective synthesis of a (5R,6S)-6-[(R)-1-hydroxyethyl]-2-aryloxy penem
3. New synthesis of penems via a reductive cyclization reaction of oxalimides with trialkyl phosphite.
4. Desulphurative approaches to penem antibiotics. II. 4-acyldithioazetidin-2-ones from penicillin derived sulphenimides, thiolsulphonates and disulphides.
5. Studies on β-lactam antibiotics. I. A novel conversion of penicillins into cephalosporins
6. An efficient synthesis of 2-substituted-thio-6-hydroxyethyl-penem-3-carboxylic acids via 2-thioxopenams