Journalartikel

Jahr der Veröffentlichung: 2007

Seiten: 5919-5922

Zeitschrift: Tetrahedron Letters

Bandnummer: 48

Heftnummer: 33

DOI Link: https://doi.org/10.1016/j.tetlet.2007.06.011

Verlag: Elsevier

Abstract: 

Two cyclopentadienones were generated and both underwent conrotatory
electrocyclization as expected based on Woodward–Hoffmann rules. This
result lends support to the idea that these ring-closing reactions are,
in fact, pericyclic processes.

Harvard-Zitierstil: Harmata, M., Zheng, P., Schreiner, P. and Navarro-Vazquez, A. (2007) Diastereoselectivity in an electrocyclization reaction of cyclopentadienones, Tetrahedron Letters, 48(33), pp. 5919-5922. https://doi.org/10.1016/j.tetlet.2007.06.011

APA-Zitierstil: Harmata, M., Zheng, P., Schreiner, P., & Navarro-Vazquez, A. (2007). Diastereoselectivity in an electrocyclization reaction of cyclopentadienones. Tetrahedron Letters. 48(33), 5919-5922. https://doi.org/10.1016/j.tetlet.2007.06.011