Trifluormethanesulfonic imidazolide : a convenient reagent for introducing the triflate group

dc.contributor.author	Effenberger, Franz	de
dc.contributor.author	Mack, Karl Ernst	de
dc.date.accessioned	2009-07-22	de
dc.date.accessioned	2016-03-31T07:47:24Z
dc.date.available	2009-07-22	de
dc.date.available	2016-03-31T07:47:24Z
dc.date.issued	1970	de
dc.date.updated	2013-06-14	de
dc.description.abstract	In all investigations of solvolysis reactions, the trifluormetbanesulfonate (triflate)anion has proven the best leaving group. (l-3) While a series of alkyl and alkenyl triflates have already been synthesized, little is known about aryl triflates the solvolysis of which we are investigating.	en
dc.identifier.other	314613757	de
dc.identifier.uri	http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41873	de
dc.identifier.uri	http://elib.uni-stuttgart.de/handle/11682/1018
dc.identifier.uri	http://dx.doi.org/10.18419/opus-1001
dc.language.iso	en	de
dc.rights	info:eu-repo/semantics/openAccess	de
dc.subject.classification	Trifluormethansulfonylgruppe , Imidazol	de
dc.subject.ddc	540	de
dc.title	Trifluormethanesulfonic imidazolide : a convenient reagent for introducing the triflate group	en
dc.type	article	de
ubs.fakultaet	Fakultät Chemie	de
ubs.institut	Institut für Organische Chemie	de
ubs.opusid	4187	de
ubs.publikation.source	Tetrahedron Letters (1970), S. 3947-3948. URL http://dx.doi.org./10.1016/S0040-4039(01)98633-2	de
ubs.publikation.typ	Zeitschriftenartikel	de

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