Journal article
Authors list: Schreiner, PR; Prall, M; Lutz, V
Publication year: 2003
Pages: 5757-5760
Journal: Angewandte Chemie International Edition
Volume number: 42
Issue number: 46
ISSN: 1433-7851
DOI Link: https://doi.org/10.1002/anie.200351195
Publisher: Wiley
Complementary products: the electrophilic cyclizations of ortho‐benzooligoynes
Abstract:
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.
Citation Styles
Harvard Citation style: 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 Citation style: 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
