Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/148218
Title: Enantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickel
Authors: Huang, Xiaolei
Teng, Shenghan
Chi, Robin Yonggui
Xu, Wenqiang
Pu, Maoping
Wu, Yun-Dong
Zhou, Steve Jianrong
Keywords: Science
Issue Date: 2021
Source: Huang, X., Teng, S., Chi, R. Y., Xu, W., Pu, M., Wu, Y. & Zhou, S. J. (2021). Enantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickel. Angewandte Chemie International Edition, 60(6), 2828-2832. https://dx.doi.org/10.1002/anie.202011036
Journal: Angewandte Chemie International Edition
Abstract: Nickel-catalyzed intermolecular Heck reaction of cycloalkenes proceeds well with aryl triflates, mesylates and tosylates in excellent enantiomeric ratios. The asymmetric reductive Heck reaction also works with a 2-cyclopentenone ketal, which is equivalent to conjugate arylation of the enone itself.
URI: https://hdl.handle.net/10356/148218
ISSN: 1521-3773
DOI: 10.1002/anie.202011036
Rights: This is the peer reviewed version of the following article: Huang, X., Teng, S., Chi, R. Y., Xu, W., Pu, M., Wu, Y. & Zhou, S. J. (2021). Enantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickel. Angewandte Chemie International Edition, 60(6), 2828-2832. https://dx.doi.org/10.1002/anie.202011036, which has been published in final form at https://doi.org/10.1002/anie.202011036. 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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