Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104148
Title: A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes
Authors: Fang, Xinqiang
Kun, Jiang
Xing, Chong
Hao, Lin
Chi, Robin Yonggui
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2011
Source: Fang, X., Kun, J., Xing, C., Hao, L., & Chi, Y. R. (2011). A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes. Angewandte Chemie International Edition, 50(8), 1910–1913.
Series/Report no.: Angewandte Chemie international edition
Abstract: Three stereogenic centers in a row: The unconventional activation of enal compounds mediated by an N-heterocyclic carbene (NHC) has generated three consecutive reactive carbon centers that undergo highly regio- and stereoselective annulations with di(enone)s to generate benzotricyclic products containing multiple stereogenic centers (see scheme).
URI: https://hdl.handle.net/10356/104148
http://hdl.handle.net/10220/19454
DOI: 10.1002/anie.201007144
Rights: © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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