4414 15 archive 337 disk0/00/00/44/14 2008-04-07 14:38:25 2008-12-09 01:15:00 2008-07-16 17:06:58 article show Michael.Gardiner@utas.edu.au Gardiner MG Michael.Gardiner@utas.edu.au Jones RC Roderick.Jones@utas.edu.au Ng M Sarah.Ng@utas.edu.au Smith JA Jason.Smith@utas.edu.au pub 030503 250301 970103 780103 public The definitive version is available at www.blackwell-synergy.com (IA 9/12/08) The Creative Commons Attribution Licence applies to all articles published in Acta Crystallographica Section E http://journals.iucr.org/e/journalhomepage.html category => A1 categoryDesc => Refereed Article in a Scholarly Journal eprintID => 0 field1 => Acta Crystallographica Section E field10 => field11 => field12 => field13 => field2 => Oxford field3 => 63 field4 => 1 field5 => o197-0199 field6 => Blackwell Publishing field7 => 1600-5368 field8 => field9 => funding => A grant => lastUpdate => 13/03/2007 rfcd => 250301 seo => 780103 themeArea => FT title => "Methyl 4-chloro-3,5-di-p-tolyl-1H-pyrrole-2-carboxylate dichloromethane hemisolvate" tor => SB uid => 43491 update => no Recently, we have developed a synthetic procedure that allows the controlled formation of mono- and diarylpyrroles by chemoselective Suzuki–Miyaura coupling (Smith et al., 2006). The key to the method was using chloride as a blocking group which is not very reactive for cross-coupling, and then its removal by catalytic hydrogenation. 2007 published Acta Crystallographica Section E 63 1 Blackwell Publishing o197-0199 10.1107/S1600536806052202 TRUE 1600-5368 http://dx.doi.org/10.1107/S1600536806052202 http://creativecommons.org/licenses/by-nc/2.0/uk/ 6100 4 4414 1 application/pdf en public cc_by

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