Journal article

Diastereoselectivity in an electrocyclization reaction of cyclopentadienones


Authors listHarmata, M; Zheng, P; Schreiner, PR; Navarro-Vazquez, A

Publication year2007

Pages5919-5922

JournalTetrahedron Letters

Volume number48

Issue number33

DOI Linkhttps://doi.org/10.1016/j.tetlet.2007.06.011

PublisherElsevier


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.




Citation Styles

Harvard Citation styleHarmata, 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 Citation styleHarmata, 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


Last updated on 2025-21-05 at 14:55