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|Title:||Asymmetric synthesis of C-aliphatic homoallylic amines and biologically important cyclohexenylamine analogues||Authors:||Lee, C.-L.K.
|Issue Date:||29-Oct-2004||Citation:||Lee, C.-L.K., Ling, H.Y., Loh, T.-P. (2004-10-29). Asymmetric synthesis of C-aliphatic homoallylic amines and biologically important cyclohexenylamine analogues. Journal of Organic Chemistry 69 (22) : 7787-7789. ScholarBank@NUS Repository. https://doi.org/10.1021/jo048903o||Abstract:||An efficient method for the asymmetric synthesis of C-aliphatic homoallylic amines with up to 94% yield and 80% de is reported. Ring-closing metathesis of several chiral homoallylic amines using the second-generation Grubbs catalyst provided easy access to a wide variety of cyclohexenylamines.||Source Title:||Journal of Organic Chemistry||URI:||http://scholarbank.nus.edu.sg/handle/10635/75631||ISSN:||00223263||DOI:||10.1021/jo048903o|
|Appears in Collections:||Staff Publications|
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