144775-26-8Relevant academic research and scientific papers
A new radical route to C4-unsubstituted β-lactams
Alcaide, Benito,Rodriguez-Vicente, Alberto,Sierra, Miguel A.
, p. 163 - 166 (2007/10/03)
C4-Unsubstituted β-lactams 3 are conveniently prepared from easily available 4-formyl-β-lactams 1, in a sequential three step synthesis, using as the key step a radical reductive decarbonylation of 4-carboxy derivatives through their phenyl selenoesters 2.
Application of (+)-(1S,2S)-2-amino-1-phenylpropan-1,3-diol in the formal total synthesis of carbapenems, novel 4-cyano-β-lactams and β-hydroxy aspartates
Jayaraman, Muthusamy,Deshmukh, Rakeep,Bhawal, Baburao M.
, p. 8989 - 9004 (2007/10/03)
The imines derived from (+)-(1S,2S)-2-amino-1-phenylpropan-1,3-diol furnished cis-β-lactams stereoselectively on the Staudinger reaction. These homochiral cis-β-lactams were converted in to cis-β-lactams possessing aminol side chain at C-4. These aminols
