TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones
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.
Saved in:
| Main Authors: | , , , , |
|---|---|
| Other Authors: | |
| Format: | Article |
| Language: | English |
| Published: |
2013
|
| Subjects: | |
| Online Access: | https://hdl.handle.net/10356/99751 http://hdl.handle.net/10220/17645 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Nanyang Technological University |
| Language: | English |
| id |
sg-ntu-dr.10356-99751 |
|---|---|
| record_format |
dspace |
| spelling |
sg-ntu-dr.10356-997512020-03-07T12:34:48Z TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones Zhu, Xu Wang, Yi-Feng Ren, Wei Zhang, Feng-Lian Chiba, Shunsuke School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry 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. 2013-11-15T02:08:48Z 2019-12-06T20:11:01Z 2013-11-15T02:08:48Z 2019-12-06T20:11:01Z 2013 2013 Journal Article 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. https://hdl.handle.net/10356/99751 http://hdl.handle.net/10220/17645 10.1021/ol4014969 en Organic letters |
| institution |
Nanyang Technological University |
| building |
NTU Library |
| country |
Singapore |
| collection |
DR-NTU |
| language |
English |
| topic |
DRNTU::Science::Chemistry::Organic chemistry |
| spellingShingle |
DRNTU::Science::Chemistry::Organic chemistry Zhu, Xu Wang, Yi-Feng Ren, Wei Zhang, Feng-Lian Chiba, Shunsuke TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| description |
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. |
| author2 |
School of Physical and Mathematical Sciences |
| author_facet |
School of Physical and Mathematical Sciences Zhu, Xu Wang, Yi-Feng Ren, Wei Zhang, Feng-Lian Chiba, Shunsuke |
| format |
Article |
| author |
Zhu, Xu Wang, Yi-Feng Ren, Wei Zhang, Feng-Lian Chiba, Shunsuke |
| author_sort |
Zhu, Xu |
| title |
TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| title_short |
TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| title_full |
TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| title_fullStr |
TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| title_full_unstemmed |
TEMPO-mediated aliphatic C–H oxidation with oximes and hydrazones |
| title_sort |
tempo-mediated aliphatic c–h oxidation with oximes and hydrazones |
| publishDate |
2013 |
| url |
https://hdl.handle.net/10356/99751 http://hdl.handle.net/10220/17645 |
| _version_ |
1681037970987024384 |