Synthesis of Rumphellaone A and Hushinone by a Gold-Catalyzed [2 + 2] Cycloaddition

All of RECERCAT

Use this identifier to quote or link this document: http://hdl.handle.net/2072/326401

dc.contributor.author	Ranieri, Beatrice
dc.contributor.author	Obradors, Carla
dc.contributor.author	Mato, Mauro
dc.contributor.author	Echavarren, Antonio M.
dc.date.accessioned	2018-06-15T12:03:25Z
dc.date.available	2018-06-15T12:03:25Z
dc.date.issued	2016-05-14
dc.identifier.uri	http://hdl.handle.net/2072/326401
dc.format.extent	1614 p.
dc.language.iso	cat
dc.rights	L'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons: http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.source	RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.subject.other	Quimica
dc.title	Synthesis of Rumphellaone A and Hushinone by a Gold-Catalyzed [2 + 2] Cycloaddition
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/draft
dc.embargo.terms	cap
dc.relation.projectID	321066
dc.identifier.doi	10.1021/acs.orglett.6b00473
dc.rights.accessLevel	info:eu-repo/semantics/openAccess
dc.description.abstract	The enantioselective total synthesis of rumphellaone A has been accomplished in 12 steps via a diastereoselective gold(I)-catalyzed [2 + 2] macrocyclization of a 1,10-enyne as the key step to build the cyclobutene moiety. This concise approach has also led to the total synthesis of husinone.

Files	Size	Format
12.-acs.orglett.6b00473.pdf	1.005 MB	PDF