Please use this identifier to cite or link to this item:
|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
|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
|ISSN:||0947-6539||DOI:||http://dx.doi.org/10.1002/chem.201201318||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.