Application of a double Mannich reaction using bis(aminol) ethers in the synthesis of AE ring analogues of methyl lycaconitine

Brocke, Constanze; Brimble, MA; Lin, DSH; McLeod, MD

dc.contributor.author	Brocke, Constanze	en
dc.contributor.author	Brimble, MA	en
dc.contributor.author	Lin, DSH	en
dc.contributor.author	McLeod, MD	en
dc.date.accessioned	2011-09-19T01:34:25Z	en
dc.date.issued	2004	en
dc.identifier.citation	SYNLETT 2359-2363 03 Nov 2004	en
dc.identifier.issn	0936-5214	en
dc.identifier.uri	http://hdl.handle.net/2292/8058	en
dc.description.abstract	An efficient method for the construction of azabicyclo[3.3.1]nonanes and azabicyclo[3.2.1]octanes is reported via double Mannich reaction of cyclic ketoesters with bis(aminol) ethers. This method is applied to the synthesis of AE ring analogues of me	en
dc.language	EN	en
dc.publisher	GEORG THIEME VERLAG KG	en
dc.relation.ispartofseries	Synlett	en
dc.rights	Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0936-5214/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.subject	Mannich reaction	en
dc.subject	aminoalkylation	en
dc.subject	bis(aminol) ethers	en
dc.subject	methyl lycaconitine	en
dc.subject	alkaloids	en
dc.subject	TRICYCLIC ANALOGS	en
dc.subject	TERTIARY-AMINES	en
dc.subject	B-RING	en
dc.subject	METHYLLYCACONITINE	en
dc.subject	BASES	en
dc.subject	HYDROLYSIS	en
dc.subject	METATHESIS	en
dc.subject	ALKALOIDS	en
dc.subject	CHEMISTRY	en
dc.subject	ACYLATION	en
dc.title	Application of a double Mannich reaction using bis(aminol) ethers in the synthesis of AE ring analogues of methyl lycaconitine	en
dc.type	Journal Article	en
dc.identifier.doi	10.1055/s-2004-831340	en
pubs.issue	13	en
pubs.begin-page	2359	en
pubs.volume	2004	en
dc.rights.holder	Copyright: Georg Thieme Verlag Stuttgart New York	en
pubs.end-page	2363	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	7665	en
pubs.org-id	Science	en
pubs.org-id	Chemistry	en
pubs.org-id	Science Research	en
pubs.org-id	Maurice Wilkins Centre (2010-2014)	en
pubs.record-created-at-source-date	2010-09-01	en