Allylic amination by the Lewis-acid-mediated ene reaction of diethyl azodicarboxylate with alkenes

Brimble, Margaret; Heathcock, CH

dc.contributor.author	Brimble, Margaret	en
dc.contributor.author	Heathcock, CH	en
dc.date.accessioned	2011-09-19T00:16:00Z	en
dc.date.issued	1993	en
dc.identifier.citation	J ORG CHEM 58(19):5261-5263 10 Sep 1993	en
dc.identifier.issn	0022-3263	en
dc.identifier.uri	http://hdl.handle.net/2292/8047	en
dc.description.abstract	The ene reaction2 plays an important role in organic synthesis as a method for carbon-carbon bond formation. Because there are a variety of enophiles available, the ene reaction converts readily accessible alkenes into more functionalized compounds in which the double bond undergoes allylic transposition. ...	en
dc.language	EN	en
dc.publisher	AMER CHEMICAL SOC	en
dc.relation.ispartofseries	Journal of Organic Chemistry	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/0022-3263/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.subject	ORGANIC-SYNTHESIS	en
dc.subject	BOND	en
dc.title	Allylic amination by the Lewis-acid-mediated ene reaction of diethyl azodicarboxylate with alkenes	en
dc.type	Journal Article	en
dc.identifier.doi	10.1021/jo00071a042	en
pubs.issue	19	en
pubs.begin-page	5261	en
pubs.volume	58	en
dc.rights.holder	Copyright: 1993 American Chemical Society	en
pubs.end-page	5263	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	140377	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	2011-10-06	en