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Please use this identifier to cite or link to this item: https://doi.org/10.1021/jo048903o
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dc.titleAsymmetric synthesis of C-aliphatic homoallylic amines and biologically important cyclohexenylamine analogues
dc.contributor.authorLee, C.-L.K.
dc.contributor.authorLing, H.Y.
dc.contributor.authorLoh, T.-P.
dc.date.accessioned2014-06-23T05:32:43Z
dc.date.available2014-06-23T05:32:43Z
dc.date.issued2004-10-29
dc.identifier.citationLee, 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
dc.identifier.issn00223263
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75631
dc.description.abstractAn 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/jo048903o
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/jo048903o
dc.description.sourcetitleJournal of Organic Chemistry
dc.description.volume69
dc.description.issue22
dc.description.page7787-7789
dc.description.codenJOCEA
dc.identifier.isiut000224707900057
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