Reversal of stereochemistry in a two-step Staudinger reaction by changing the backbone protecting group. Synthesis of NH-trans-3-benzoyloxy-4-aryl-azetidinones - Concepedia

Concepedia

Publication | Closed Access

Reversal of stereochemistry in a two-step Staudinger reaction by changing the backbone protecting group. Synthesis of NH-trans-3-benzoyloxy-4-aryl-azetidinones

20

Citations

18

References

1999

Year

Mauro Panunzio, Sergio Bacchi, Eileen Campana, Laura Flume, Paola Vicennati

Tetrahedron Letters

EngineeringTwo-step Staudinger ReactionOrganic ChemistryStereoselective SynthesisChemistrySynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering

References

	Year	Citations

Page 1