Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines
Under control: The first example of chiral amino phosphine catalysts for the title reaction between vinyl ketones and N-sulfonyl-1-aza-1,3-dienes has been developed. Under ambient conditions, this protocol provides straightforward access to densely functionalized, enantioenriched tetrahydropyridines...
| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Journal Article |
| Language: | English |
| Published: |
2013
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| Online Access: | https://hdl.handle.net/10356/98453 http://hdl.handle.net/10220/12444 |
| _version_ | 1811681225813786624 |
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| author | Shi, Zugui Yu, Peiyuan Loh, Teck-Peng Zhong, Guofu |
| author2 | School of Physical and Mathematical Sciences |
| author_facet | School of Physical and Mathematical Sciences Shi, Zugui Yu, Peiyuan Loh, Teck-Peng Zhong, Guofu |
| author_sort | Shi, Zugui |
| collection | NTU |
| description | Under control: The first example of chiral amino phosphine catalysts for the title reaction between vinyl ketones and N-sulfonyl-1-aza-1,3-dienes has been developed. Under ambient conditions, this protocol provides straightforward access to densely functionalized, enantioenriched tetrahydropyridines with high levels of sterecontrol in good to excellent yields. |
| first_indexed | 2024-10-01T03:37:34Z |
| format | Journal Article |
| id | ntu-10356/98453 |
| institution | Nanyang Technological University |
| language | English |
| last_indexed | 2024-10-01T03:37:34Z |
| publishDate | 2013 |
| record_format | dspace |
| spelling | ntu-10356/984532020-03-07T12:34:47Z Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines Shi, Zugui Yu, Peiyuan Loh, Teck-Peng Zhong, Guofu School of Physical and Mathematical Sciences Under control: The first example of chiral amino phosphine catalysts for the title reaction between vinyl ketones and N-sulfonyl-1-aza-1,3-dienes has been developed. Under ambient conditions, this protocol provides straightforward access to densely functionalized, enantioenriched tetrahydropyridines with high levels of sterecontrol in good to excellent yields. 2013-07-29T04:43:56Z 2019-12-06T19:55:23Z 2013-07-29T04:43:56Z 2019-12-06T19:55:23Z 2012 2012 Journal Article Shi, Z., Yu, P., Loh, T. P., & Zhong, G. (2012). Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines. Angewandte Chemie International Edition, 51(31), 7825-7829. 1433-7851 https://hdl.handle.net/10356/98453 http://hdl.handle.net/10220/12444 10.1002/anie.201203316 en Angewandte chemie international edition © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| spellingShingle | Shi, Zugui Yu, Peiyuan Loh, Teck-Peng Zhong, Guofu Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title | Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title_full | Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title_fullStr | Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title_full_unstemmed | Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title_short | Catalytic asymmetric [4+2] annulation initiated by an Aza-Rauhut-Currier reaction : facile entry to highly functionalized tetrahydropyridines |
| title_sort | catalytic asymmetric 4 2 annulation initiated by an aza rauhut currier reaction facile entry to highly functionalized tetrahydropyridines |
| url | https://hdl.handle.net/10356/98453 http://hdl.handle.net/10220/12444 |
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