Extending the Range of Neutral N-Donor Ligands Available for Metal Catalysts: N-[1-Alkylpyridin-4(1H)-ylidene]amides in Palladium-Catalyzed Cross-Coupling Reactions

Boyd, Peter; Wright, Leonard; Zafar, MN

dc.contributor.author	Boyd, Peter	en
dc.contributor.author	Wright, Leonard	en
dc.contributor.author	Zafar, MN	en
dc.date.accessioned	2011-10-26T02:49:13Z	en
dc.date.issued	2011-09	en
dc.identifier.citation	Inorganic Chemistry Sep 2011	en
dc.identifier.issn	0020-1669	en
dc.identifier.uri	http://hdl.handle.net/2292/8444	en
dc.description.abstract	N-[1-Alkylpyridin-4(1H)-ylidene]amides (PYAs) are a new class of easily prepared, neutral N-donor ligands that share some features in common with N-heterocyclic carbenes. They are strongly electron-donating toward metal centers, and a palladium(II) complex of one of these ligands has been shown to successfully catalyze both the Heck-Mizoroki and Suzuki-Miyaura cross-coupling reactions.	en
dc.language	ENG	en
dc.publisher	American Chemical Society	en
dc.relation.ispartofseries	Inorganic 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. http://www.sherpa.ac.uk/romeo/issn/0020-1669/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.title	Extending the Range of Neutral N-Donor Ligands Available for Metal Catalysts: N-[1-Alkylpyridin-4(1H)-ylidene]amides in Palladium-Catalyzed Cross-Coupling Reactions	en
dc.type	Journal Article	en
dc.identifier.doi	10.1021/ic201527s	en
pubs.begin-page	10522	en
pubs.volume	50	en
dc.rights.holder	Copyright: American Chemical Society	en
dc.identifier.pmid	21961733	en
pubs.end-page	10524	en
pubs.publication-status	Published	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	232988	en
pubs.org-id	Science	en
pubs.org-id	Chemistry	en
dc.identifier.eissn	1520-510X	en
pubs.record-created-at-source-date	2011-10-25	en
pubs.dimensions-id	21961733	en