Journal article

Deantiaromatization as a driving force in an electrocyclic reaction


Authors list: Harmata, M; Zheng, P; Schreiner, PR; Navarro-Vazquez, A

Publication year: 2006

Pages: 1966-1971

Journal: Angewandte Chemie International Edition

Volume number: 45

Issue number: 12

ISSN: 1433-7851

DOI Link: https://doi.org/10.1002/anie.200503812

Publisher: Wiley


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.




Citation Styles

Harvard Citation style: Harmata, 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 Citation style: Harmata, 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


Last updated on 2025-21-05 at 13:32