TY  - BOOK
AU  - Tengho Toguem, Serge-Mithérand
PY  - 2011
DA  - 2011//
TI  - Twofold Heck
AB  - This thesis presents site-selective Suzuki-Miyaura reactions of 2,3,5-tribromo-thiophene, 2,4,5-tribromothiophene and 2,3,5-tribromo-N-methylpyrrole, which are controlled by steric and electronic parameters. Palladium-catalyzed Heck reactions of brominated thiophenes, N-methylimidazole, N-methylpyrrole and N-methylindole are also presented. The products were transformed by subsequent 6p-electrocyclization and dehydrogenation to functionalized benzothiophenes, dibenzothiophenes, benzimidazoles, indoles and carbazoles, respectively.
UR  - http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2012-0025-5
UR  - http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2012-0025-5&pdf
UR  - http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2012-0025-5
LA  - English
N1  - 6π-electrocyclization and regioselective palladium(0)-catalyzed reactions of brominated thiophenes, pyrroles, imidazoles and indoles / vorgelegt von Serge-Mithérand Tengho Toguem
ID  - 687893097
ER  -