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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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