130075-03-5Relevant academic research and scientific papers
An approach to carbapenems from α,β-unsaturated sugar lactones
Maciejewski,Panfil,Belzecki,Chmielewski
, p. 10363 - 10376 (2007/10/02)
Conjugate addition-rearrangement of N-substituted hydroxylamines to α,β-unsaturated D-lactones provides a short and effective route to 3-substituted isoxazolidin-5-ones. These compounds were converted into 4-substituted azetidin-2-ones via a two-step proc
Synthesis of enantiomerically pure precursors of carbapenems from carbohydrates
Maciejewski, Sylwester,Panfil, Irma,Belzecki, Czeslaw,Chimielewski, Marek
, p. 1901 - 1902 (2007/10/02)
Conjugate addition-rearrangement of N-p-metoxybenzylhydroxylamine to α,β-unsaturated sugar lactones followed by hydrogenolysis of the O-N bond in isoxazolidin-5-ones, and subsequent cyclization of the resulting β-amino acid, provides an effective route to
