Rotational spectra of tetracyclic quinolizidine alkaloids: does a water molecule flip sparteine?

Author:

Lesarri Alberto12345ORCID,Pinacho Ruth67345ORCID,Enríquez Lourdes67345ORCID,Rubio José E.67345ORCID,Jaraíz Martín67345ORCID,Abad José L.89101112ORCID,Gigosos Marco A.1314234ORCID

Affiliation:

1. Departamento de Química Física y Química Inorgánica

2. Facultad de Ciencias

3. Universidad de Valladolid

4. 47011 Valladolid

5. Spain

6. Departamento de Electrónica

7. Escuela de Ingeniería de Telecomunicaciones

8. Spanish National Research Council (CSIC)

9. Institute of Advanced Chemistry of Catalonia (IQAC-CSIC)

10. Research Unit on Bioactive Molecules (RUBAM)

11. Department of Biomedicinal Chemistry

12. 08034 Barcelona

13. Departamento de Física Teórica

14. Atómica y Óptica

Abstract

Flipping or not flipping? The sparteine–water dimer generated in a jet expansion retains the trans conformation of the parent molecule.

Funder

Secretaría de Estado de Investigación, Desarrollo e Innovación

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference54 articles.

1. N. J. Leonard , in The Alkaloids, Chemistry and Physiology, ed. R. H. F. Manske and H. L. Holmes, Academic Press, New York, vol. III, 1953

2. T. Aniszewski , Alkaloids, Chemistry, Biology, Ecology and Applications, Elsevier, Amsterdam, 2nd edn, 2015

3. The Total Synthesis of Sparteine and an Isosparteine by Reductive Cyclization1

4. A stereoselective synthesis of α-isosparteine

5. Biosynthesis of the lupine alkaloids. II. Sparteine and lupanine

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