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

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Utilizad este identificador para citar o enlazar este documento: 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.

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García-Morales, Cristina; Ranieri, Beatrice; Escofet, Imma; Loṕez-Suarez, Laura; Obradors, Carla; Konovalov, Andrey I.; Echavarren, Antonio M.

Calleja, Pilar; Pablo, Óscar; Ranieri, Beatrice; Gaydou, Morgane; Pitaval, Anthony; Moreno, María; Raducan, Mihai; Echavarren, Antonio M.

Mato, Mauro; Echavarren, Antonio M.

Mato, Mauro; García-Morales, Cristina; Echavarren, Antonio M.

Armengol-Relats, Helena; Mato, Mauro; Echavarren, Antonio M.

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