TY  - JOUR
N1  - The definitive version is available at www.blackwell-synergy.com
ID  - epprod4414
UR  - http://dx.doi.org/10.1107/S1600536806052202
IS  - 1
A1  - Gardiner, MG
A1  - Jones, RC
A1  - Ng, M
A1  - Smith, JA
Y1  - 2007///
N2  - 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.
PB  - Blackwell Publishing
JF  - Acta Crystallographica Section E
VL  - 63
SN  - 1600-5368
TI  - Methyl 4-chloro-3,5-di-p-tolyl-1H-pyrrole-2-carboxylate dichloromethane hemisolvate
SP  - o197
AV  - public
EP  - 0199
ER  -