Nucleophilic aromatic substitution : a new synthetic route to biphenyls

dc.contributor.author	Effenberger, Franz	de
dc.contributor.author	Nagel, Klaus	de
dc.contributor.author	Agster, Wolfgang	de
dc.date.accessioned	2009-10-26	de
dc.date.accessioned	2016-03-31T07:47:56Z
dc.date.available	2009-10-26	de
dc.date.available	2016-03-31T07:47:56Z
dc.date.issued	1971	de
dc.date.updated	2014-09-26	de
dc.description.abstract	The most important methods for preparation of biphenyls are the Ullmann and Gomberg reactions, which involve radical or organometallic intermediates; furthermore, biaryls are formed by benzidine rearrangement and oxidative dimerization, as well as in the course of reactions involving aryne intermediates.	en
dc.identifier.other	318085305	de
dc.identifier.uri	http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41925	de
dc.identifier.uri	http://elib.uni-stuttgart.de/handle/11682/1238
dc.identifier.uri	http://dx.doi.org/10.18419/opus-1221
dc.language.iso	en	de
dc.rights	info:eu-repo/semantics/openAccess	de
dc.subject.classification	Biphenylderivate , Substitutionsreaktion	de
dc.subject.ddc	540	de
dc.title	Nucleophilic aromatic substitution : a new synthetic route to biphenyls	en
dc.type	article	de
ubs.fakultaet	Fakultät Chemie	de
ubs.institut	Institut für Organische Chemie	de
ubs.opusid	4192	de
ubs.publikation.source	Angewandte Chemie, International edition 10 (1971), S. 566-567. URL http://dx.doi.org./10.1002/anie.197105662	de
ubs.publikation.typ	Zeitschriftenartikel	de

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