Enantioselective total synthesis of (R)-(−)-complanine

dc.contributor.author	Kamanos, Krystal A. D.
dc.contributor.author	Withey, Jonathan M.
dc.date.accessioned	2014-10-02
dc.date.accessioned	2022-05-27T01:13:15Z
dc.date.available	2022-05-27T01:13:15Z
dc.date.issued	2012
dc.description.abstract	A route is described for the enantioselective synthesis of (R)-(−)-complanine, a marine natural product isolated from Eurythoe complanata, and known to be a causative agent in inflammation. An organocatalytic, asymmetric oxyamination of a homoconjugated all-Z-dienal intermediate provides versatile and efficient access to the natural product.
dc.format.extent	225.73 kb
dc.format.mimetype	PDF
dc.identifier.citation	Kamanos, K. A. D. & Withey, J. M. (2012). Enantioselective total synthesis of (R)-(−)-complanine. Beilstein Journal of Organic Chemistry, 8, 1695–1699. doi:10.3762/bjoc.8.192
dc.identifier.doi	https://doi.org/10.3762/bjoc.8.192
dc.identifier.uri	https://hdl.handle.net/20.500.14078/159
dc.language	English
dc.language.iso	en
dc.rights	Attribution (CC BY)
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/
dc.subject	complanine
dc.subject	enantioselective synthesis
dc.subject	marine fireworm
dc.subject	nitrosoaldol
dc.subject	organocatalysis
dc.title	Enantioselective total synthesis of (R)-(−)-complanine	en
dc.type	Article

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