Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/99501
Title: | [4+2] Annulation of Vinyl Ketones initiated by a Phosphine-Catalyzed Aza-Rauhut-Currier reaction: a practical access to densely functionalized Tetrahydropyridines | Authors: | Zhong, Guofu Leong, Wendy Wen Yi Tong, Qinjie Shi, Zugui |
Issue Date: | 2012 | Source: | Shi, Z., Tong, Q., Leong, W. W. Y.,& Zhong, G. (2012). [4+2] Annulation of Vinyl Ketones Initiated by a Phosphine-Catalyzed Aza-Rauhut-Currier Reaction: A Practical Access to Densely Functionalized Tetrahydropyridines. Chemistry - A European Journal, 18(32), 9802-9806. | Series/Report no.: | Chemistry - a European journal | Abstract: | The first example of phosphine catalyzed aza-Rauhut–Currier reaction initiated [4+2] annulation of vinyl ketones with N-sulfonyl-1-aza-1,3-dienes has been disclosed. Under the ambient conditions, this protocol provides a practical access to valuable densely functionalized tetrahydropyridines in good to excellent yields and high diastereoselectivities (see scheme). | URI: | https://hdl.handle.net/10356/99501 http://hdl.handle.net/10220/12915 |
ISSN: | 0947-6539 | DOI: | 10.1002/chem.201201318 | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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