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https://hdl.handle.net/10356/155085
Title: | Asymmetric Wacker-type oxyallenylation and azaallenylation of cyclic alkenes | Authors: | Teng, Shenghan Jiao, Zhiwei Chi, Robin Yonggui Zhou, Steve Jianrong |
Keywords: | Science::Chemistry | Issue Date: | 2020 | Source: | Teng, S., Jiao, Z., Chi, R. Y. & Zhou, S. J. (2020). Asymmetric Wacker-type oxyallenylation and azaallenylation of cyclic alkenes. Angewandte Chemie International Edition, 59(6), 2246-2250. https://dx.doi.org/10.1002/anie.201911961 | Project: | AME IRG A1783c0010 | Journal: | Angewandte Chemie International Edition | Abstract: | Palladium-catalyzed three-component carboetherification of cyclic alkenes proceeded to give trans adducts exclusively with excellent enantioselectivity through a Wacker-type pathway. The reaction is also applicable to other oxygen nucleophiles, such as water, phenols, and carboxylic acids, as well as some electron-poor aryl amines. | URI: | https://hdl.handle.net/10356/155085 | ISSN: | 1433-7851 | DOI: | 10.1002/anie.201911961 | Rights: | This is the peer reviewed version of the following article: Teng, S., Jiao, Z., Chi, R. Y. & Zhou, S. J. (2020). Asymmetric Wacker-type oxyallenylation and azaallenylation of cyclic alkenes. Angewandte Chemie International Edition, 59(6), 2246-2250, which has been published in final form at https://doi.org/10.1002/anie.201911961. 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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