Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex

dc.contributor.author	Jurgens, Eva
dc.contributor.author	Wucher, Barbara
dc.contributor.author	Rominger, Frank
dc.contributor.author	Törnroos, Karl Wilhelm
dc.contributor.author	Kunz, Doris
dc.date.accessioned	2016-03-31T11:35:00Z
dc.date.available	2016-03-31T11:35:00Z
dc.date.issued	2014-12-22
dc.Published	Chemical Communications 2015, 51(10):1897-1900	eng
dc.identifier.issn	1364-548X	en_US
dc.identifier.uri	https://hdl.handle.net/1956/11794
dc.description.abstract	An efficient RhI–NHC–pincer catalyst for the highly regioselective Meinwald rearrangement of monoalkylated epoxides into methylketones under mild conditions is presented. The nucleophilic epoxide opening is assisted by Lewis acids.	en_US
dc.language.iso	eng	eng
dc.publisher	Royal Society of Chemistry	en_US
dc.rights	Attribution CC BY	eng
dc.rights.uri	http://creativecommons.org/licenses/by/3.0/	eng
dc.title	Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex	en_US
dc.type	Peer reviewed
dc.type	Journal article
dc.date.updated	2015-12-30T17:04:52Z
dc.description.version	publishedVersion	en_US
dc.rights.holder	Copyright 2014 the authors	en_US
dc.identifier.doi	https://doi.org/10.1039/c4cc07154a
dc.identifier.cristin	1253922
dc.subject.nsi	VDP::Matematikk og naturvitenskap: 400::Kjemi: 440::Organisk kjemi: 441
dc.subject.nsi	VDP::Mathematics and natural scienses: 400::Chemistry: 440::Organic chemistry: 441

Except where otherwise noted, this item's license is described as Attribution CC BY