Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/155086
Title: Asymmetric reductive and alkynylative heck bicyclization of enynes to access conformationally restricted aza[3.1.0]bicycles
Authors: Huang, Xiaolei
Nguyen, Minh Hieu
Pu, Maoping
Zhang, Luoqiang
Chi, Robin Yonggui
Wu, Yun-Dong
Zhou, Steve Jianrong
Keywords: Science::Chemistry
Issue Date: 2020
Source: Huang, X., Nguyen, M. H., Pu, M., Zhang, L., Chi, R. Y., Wu, Y. & Zhou, S. J. (2020). Asymmetric reductive and alkynylative heck bicyclization of enynes to access conformationally restricted aza[3.1.0]bicycles. Angewandte Chemie International Edition, 59(27), 10814-10818. https://dx.doi.org/10.1002/anie.202000859
Project: AME IRG A1783c0010
Journal: Angewandte Chemie International Edition
Abstract: Conformationally restricted azabicycles are becoming increasingly important in medicinal research. Asymmetric Heck bicyclization of enynes proceeds to give medicinally useful aza[3.1.0] and aza[4.1.0] bicycles with excellent enantioselectivity. The key organopalladium species after bicyclization can be trapped by silanes and terminal alkynes.
URI: https://hdl.handle.net/10356/155086
ISSN: 1521-3773
DOI: 10.1002/anie.202000859
Schools: School of Physical and Mathematical Sciences 
Rights: This is the peer reviewed version of the following article: Huang, X., Nguyen, M. H., Pu, M., Zhang, L., Chi, R. Y., Wu, Y. & Zhou, S. J. (2020). Asymmetric reductive and alkynylative heck bicyclization of enynes to access conformationally restricted aza[3.1.0]bicycles. Angewandte Chemie International Edition, 59(27), 10814-10818, which has been published in final form at https://doi.org/10.1002/anie.202000859. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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