Journalartikel

Deantiaromatization as a driving force in an electrocyclic reaction


AutorenlisteHarmata, M; Zheng, P; Schreiner, PR; Navarro-Vazquez, A

Jahr der Veröffentlichung2006

Seiten1966-1971

ZeitschriftAngewandte Chemie International Edition

Bandnummer45

Heftnummer12

ISSN1433-7851

DOI Linkhttps://doi.org/10.1002/anie.200503812

VerlagWiley


Abstract

Theory and experiment support the notion that “deantiaromatization” can
serve as a driving force in the 8‐π‐electron electrocyclization of a
cyclopentadienone (see scheme; TEA=triethylamine; TFE=trifluoroethanol).
The reaction proceeds in synthetically useful yields and could be
applicable to the synthesis of the antiviral agent hamigeran B.




Zitierstile

Harvard-ZitierstilHarmata, M., Zheng, P., Schreiner, P. and Navarro-Vazquez, A. (2006) Deantiaromatization as a driving force in an electrocyclic reaction, Angewandte Chemie International Edition, 45(12), pp. 1966-1971. https://doi.org/10.1002/anie.200503812

APA-ZitierstilHarmata, M., Zheng, P., Schreiner, P., & Navarro-Vazquez, A. (2006). Deantiaromatization as a driving force in an electrocyclic reaction. Angewandte Chemie International Edition. 45(12), 1966-1971. https://doi.org/10.1002/anie.200503812



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