Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/99751
Title: TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones
Authors: Zhu, Xu
Wang, Yi-Feng
Ren, Wei
Zhang, Feng-Lian
Chiba, Shunsuke
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2013
Source: Zhu, X., Wang, Y. F., Ren, W., Zhang, F. L., & Chiba, S. (2013). TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones. Organic letters, 15(13), 3214-3217.
Series/Report no.: Organic letters
Abstract: A method for aliphatic C–H bond oxidation of oximes and hydrazones mediated by 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) has been developed, which enables the concise assembly of substituted isoxazole and pyrazole skeletons.
URI: https://hdl.handle.net/10356/99751
http://hdl.handle.net/10220/17645
DOI: 10.1021/ol4014969
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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