The penems, a new class of β-lactam antibiotics. II. Total synthesis of racemic 6-unsubstituted representatives

DOI: 10.1021/ja00515a024

Source and publish data:

Journal of the American Chemical Society p. 6296 - 6301 (1979)

Update date:2022-08-05

Topics: Acylation   Yield   Chiral center   Stereochemistry   Chromatography   Total synthesis   Hydrolysis   Nucleophilic substitution   Enantiomers   Deprotection   Ring closure   Protecting group   Racemic   Retrosynthetic analysis   Stereoselectivity   Reaction Optimization   β-lactam antibiotics   Penems   Spectroscopy (NMR, IR, MS)  

Authors:

Lang

Prasad

Holick

et al.