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https://hdl.handle.net/10356/100042
Title: | Access to oxoquinoline heterocycles by N-heterocyclic carbene catalyzed ester activation for selective reaction with an enone | Authors: | Fu, Zhenqian Jiang, Ke Zhu, Tingshun Torres, Jaume Chi, Robin Yonggui |
Keywords: | DRNTU::Science::Chemistry::Inorganic chemistry::Cyclic compounds | Issue Date: | 2014 | Source: | Fu, Z., Jiang, K., Zhu, T., Torres, J., & Chi, Y. R. (2014). Access to Oxoquinoline Heterocycles by N-Heterocyclic Carbene Catalyzed Ester Activation for Selective Reaction with an Enone. Angewandte Chemie International Edition, 53(25), 6506–6510. | Series/Report no.: | Angewandte chemie international edition | Abstract: | Organocatalytic ester activation is developed for a highly selective cascade reaction between saturated esters and amino enones. The reaction involves activation of the β-carbon atom of the ester as a key step. This method allows a single-step access to multicyclic oxoquinoline-type heterocycles with high enantiomeric ratios. | URI: | https://hdl.handle.net/10356/100042 http://hdl.handle.net/10220/19652 |
ISSN: | 1433-7851 | DOI: | 10.1002/anie.201402620 | Schools: | School of Biological Sciences School of Physical and Mathematical Sciences |
Rights: | © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SBS Journal Articles SPMS Journal Articles |
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