NAGIOS: RODERIC FUNCIONANDO

Triazolopyridines 23.1 Synthesis of 5,5'-bi[1,2,3]triazolo[5,1-a]isoquinoline

Repositori DSpace/Manakin

dc.contributor.author	Abarca González, Belén
dc.contributor.author	Ballesteros Campos, Rafael
dc.contributor.author	Gay Roig, Bernat
dc.contributor.author	Domínguez, José-Reynaldo
dc.date.accessioned	2010-06-08T10:27:52Z
dc.date.available	2010-06-08T10:27:52Z
dc.date.issued	2004
dc.identifier.citation	ABARCA GONZALEZ, Belen ; Ballesteros Campos,Rafael ; Gay Roig, Bernat ; Domínguez, José-Reynaldo, 2004, Triazolopyridines 23.1 Synthesis of 5,5'-bi[1,2,3]triazolo[5,1-a]isoquinoline, Arkivoc, vol. 2004, no. IV, p. 42-47	en
dc.identifier.uri	http://hdl.handle.net/10550/12898
dc.description.abstract	5,5'-Bi[1,2,3]triazolo[5,1-a]isoquinoline 6 has been synthesised from [1,2,3]triazolo[5,1-a] isoquinoline 5 by four procedures, dimerisation by LDA, Stille and Suzuki self-coupling reactions, and Suzuki cross-coupling reaction. The last is the best. Compound 6 gives 1,1'- bi(acetoxymethyl)-3,3'-biisoquinoline 10 by triazolo ring opening by acetic acid.	en
dc.language.iso	en	en
dc.subject	Bitriazoloisoquinolines ; Triazoloisoquinolines ; Lithiation reaction ; Self-coupling and cross-coupling reactions	en
dc.title	Triazolopyridines 23.1 Synthesis of 5,5'-bi[1,2,3]triazolo[5,1-a]isoquinoline	en
dc.type	journal article	es_ES
dc.subject.unesco	UNESCO::QUÍMICA	en
dc.subject.unesco	UNESCO::QUÍMICA::Química orgánica	en
dc.identifier.idgrec	003656	en
dc.type.hasVersion	VoR	es_ES
dc.identifier.url	http://www.arkat-usa.org/get-file/19185/	en