Journalartikel

Jahr der Veröffentlichung: 2003

Seiten: 5757-5760

Zeitschrift: Angewandte Chemie International Edition

Bandnummer: 42

Heftnummer: 46

ISSN: 1433-7851

DOI Link: https://doi.org/10.1002/anie.200351195

Verlag: Wiley

Abstract: 

Complementary products: the electrophilic cyclizations of ortho‐benzooligoynes
upon bromination give benzopentafulvenes with orthogonal, peripheral
phenyl groups. In contrast, the thermal cyclizations of the same
starting materials give naphthalene derivatives. This strategy was used
for the synthesis of anellated benzopentafulvenes in domino reactions.

Harvard-Zitierstil: Schreiner, P., Prall, M. and Lutz, V. (2003) Fulvenes from enediynes: Regioselective electrophilic domino and tandem cyclizations of enynes and oligoynes, Angewandte Chemie International Edition, 42(46), pp. 5757-5760. https://doi.org/10.1002/anie.200351195

APA-Zitierstil: Schreiner, P., Prall, M., & Lutz, V. (2003). Fulvenes from enediynes: Regioselective electrophilic domino and tandem cyclizations of enynes and oligoynes. Angewandte Chemie International Edition. 42(46), 5757-5760. https://doi.org/10.1002/anie.200351195