Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/137897
Title: Carbene-catalyzed formal [3+3] cycloaddition reaction for access to substituted 2-phenylbenzothiazoles
Authors: Ni, Zhibin
Mou, Chengli
Zhu, Xun
Qi, Puying
Yang, Song
Chi, Robin Yonggui
Jin, Zhichao
Keywords: Science::Chemistry::Organic chemistry
Issue Date: 2019
Source: Ni, Z., Mou, C., Zhu, X., Qi, P., Yang, S., Chi, R. Y., & Jin, Z. (2020). Carbene-catalyzed formal [3+3] cycloaddition reaction for access to substituted 2-phenylbenzothiazoles. European Journal of Organic Chemistry, 2020(4), 492-495. doi:10.1002/ejoc.201901773
Journal: European Journal of Organic Chemistry
Abstract: A carbene-catalyzed oxidative cycloaddition reaction is developed for efficient access to multi-functionalized 2-phenylbenzothiazoles. A broad scope of heavily substituted arenes bearing 2-benzothiazole groups have been prepared in good to excellent yields. The remote C(sp2)–H bond in the substituted arene products can be activated by Pd catalysts in regio-selective fashion with the direction of the 2-benzothiazole groups.
URI: https://hdl.handle.net/10356/137897
ISSN: 1434-193X
DOI: 10.1002/ejoc.201901773
Rights: This is the peer reviewed version of the following article: Ni, Z., Mou, C., Zhu, X., Qi, P., Yang, S., Chi, R. Y., & Jin, Z. (2020). Carbene-catalyzed formal [3+3] cycloaddition reaction for access to substituted 2-phenylbenzothiazoles. European Journal of Organic Chemistry, 2020(4), 492-495, which has been published in final form at https://doi.org/10.1002/ejoc.201901773. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Fulltext Permission: embargo_20210207
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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