Please use this identifier to cite or link to this item: 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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