Projects funded by the NCN
Studies on the stereoselective 1,3-Dipolar cycloaddition reactions of cyclic nitrones with alpha, beta - unsaturated lactones. Synthesis of carbapenams and carbapenems.
2014/13/N/ST5/01758
Keywords:
1,3-dipolar cycloaddition diastereoselective reactions beta-lactamic compounds antibiotics
Descriptors:
- ST5_23:
- ST5_16:
Panel:
ST5 - Materials: materials synthesis, structure-properties relations, advanced and functional materials with designed properties, (macro)molecular architecture, material engineering
Host institution :
Instytut Chemii Organicznej PAN
woj. mazowieckie
Principal investigator (from the host institution):
Number of co-investigators in the project: 2
Call: PRELUDIUM 7 - announced on 2014-03-17
Amount awarded: 97 500 PLN
Project start date (Y-m-d): 2015-01-27
Project end date (Y-m-d): 2017-01-26
Project duration:: 24 months (the same as in the proposal)
Project status: Project settled
Information in the final report
- Publication in academic press/journals (2)
- Formal synthesis of ThienamycinAuthors:M. Pieczykolan, B. Furman, M. ChmielewskiAcademic press:The Journal of Antibiotics (rok: 2017, tom: 70, strony: 781-787), Wydawca: Nature Publishing GroupStatus:PublishedDOI:10.1038/ja.2017.44 - link to the publication
- 1,3-Dipolar cycloaddition of a cyclic nitrone derived from 2-deoxy-D-ribose to α,β-unsaturated lactones: An entry to carbapenem antibioticsAuthors:M. Pieczykolan, O. Staszewska-Krajewska, B. Furman, M. ChmielewskiAcademic press:Carbohydrate Research (rok: 2016, tom: 433, strony: 89-96), Wydawca: ElsevierStatus:PublishedDOI:10.1016/j.carres.2016.07.002 - link to the publication