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Methyl 4-chloro-3,5-di-p-tolyl-1H-pyrrole-2-carboxylate dichloromethane hemisolvate

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Gardiner, MG and Jones, Roderick C and Ng, M and Smith, JA (2007) Methyl 4-chloro-3,5-di-p-tolyl-1H-pyrrole-2-carboxylate dichloromethane hemisolvate. Acta Crystallographica Section E, 63 (1). o197-0199. ISSN 1600-5368

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Abstract

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.

Item Type: Article
Journal or Publication Title: Acta Crystallographica Section E
Publisher: Blackwell Publishing
Page Range: o197-0199
ISSN: 1600-5368
Identification Number - DOI: 10.1107/S1600536806052202
Additional Information:

The definitive version is available at www.blackwell-synergy.com

Date Deposited: 07 Apr 2008 14:38
Last Modified: 18 Nov 2014 03:35
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