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From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: a view in perspective

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From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: a view in perspective

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dc.contributor.author	Medio Simón, Mercedes
dc.contributor.author	Alemán López, Pedro Antonio
dc.contributor.author	Cuenca González, Ana Belén
dc.contributor.author	Gil Tomás, Jesús Javier
dc.contributor.author	Rodriguez, Nuria
dc.contributor.author	Asensio Aguilar, Gregorio
dc.date.accessioned	2010-06-08T10:27:12Z
dc.date.available	2010-06-08T10:27:12Z
dc.date.issued	2005
dc.identifier.citation	Medio Simón, Mercedes ; Aleman Lopez, Pedro Antonio ; Cuenca Gonzalez, Ana Belen ; Gil Tomás, Jesús Javier ; Rodriguez, Nuria ; Asensio Aguilar, Gregorio ; 2005, From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: a view in perspective, Arkivoc, vol. 2005, no. IX, p. 266-286	en
dc.identifier.uri	http://hdl.handle.net/10550/12897
dc.description.abstract	A general study of the enantioselective protonation of prochiral enolates with 2-sulfinyl alcohols is reported. The modification of reaction conditions to reduce drastically the amount of chiral proton source needed to obtain a good enantiomeric excess is reported. The effects of the different factors controlling the stereoselectivity are clearly established. Different protocols for enolate generation are compared.	en
dc.language.iso	en	en
dc.subject	Enolates ; Enantioselective protonation ; Sulfinyl alcohols	en
dc.title	From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: a view in perspective	en
dc.type	journal article	es_ES
dc.subject.unesco	UNESCO::QUÍMICA	en
dc.subject.unesco	UNESCO::QUÍMICA::Química orgánica	en
dc.identifier.idgrec	027487	en
dc.type.hasVersion	VoR	es_ES
dc.identifier.url	http://www.arkat-usa.org/get-file/18922/	en