TY  - JOUR
A1  - Schmidt, Bernd
A1  - Elizarov, Nelli
A1  - Riemer, Nastja
A1  - Hölter, Frank
T1  - Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalization
JF  - European journal of organic chemistry
N2  - Unlike their ortho counterparts, meta- and para-acetamidoanilines can be converted into the corresponding acetamidoarenediazonium salts. These offer various opportunities for multiple Pd-catalyzed arene functionalization reactions, such as Matsuda-Heck-, Suzuki-Miyaura- or Fujiwara-Moritani couplings.
KW  - Arenes
KW  - Amides
KW  - C-C coupling
KW  - Cross-coupling
KW  - Palladium
Y1  - 2015
U6  - https://doi.org/10.1002/ejoc.201500795
SN  - 1434-193X
SN  - 1099-0690
IS  - 26
SP  - 5826
EP  - 5841
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Schmidt, Bernd
A1  - Hölter, Frank
T1  - Suzuki-Miyaura cross coupling reactions with Phenoldiazonium salts
JF  - Organic & biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry
N2  - The Suzuki-Miyaura coupling of phenol diazonium salts and aryl trifluoroborates yields 4-hydroxybiaryls in a protecting group-free synthesis.
Y1  - 2011
U6  - https://doi.org/10.1039/c1ob05256j
SN  - 1477-0520
VL  - 9
IS  - 13
SP  - 4914
EP  - 4920
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Schmidt, Bernd
A1  - Elizarov, Nelli
A1  - Berger, René
A1  - Hölter, Frank
T1  - Scope and limitations of the Heck-Matsuda-coupling of phenol diazonium salts and styrenes: a protecting-group economic synthesis of phenolic stilbenes
N2  - 4-Phenol diazonium salts undergo Pd-catalyzed Heck reactions with various styrenes to 4ï-hydroxy stilbenes. In almost all cases higher yields and fewer side products were observed, compared to the analogous 4-methoxy benzene diazonium salts. In contrast, the reaction fails completely with 2- and 3-phenol diazonium salts. For these substitution patterns the methoxy-substituted derivatives are superior.
Y1  - 2014
UR  - http://pubs.rsc.org/en/content/articlepdf/2013/ob/c3ob40420j
U6  - https://doi.org/10.1039/C3OB40420J
SN  - 1477-0520
ER  - 
TY  - THES
A1  - Hölter, Frank
T1  - Synthese phenologischer Diazoniumsalze und ihre Anwendung in Palladium-kristalisierten Kupplungsreaktionen
Y1  - 2011
CY  - Potsdam
ER  - 
TY  - GEN
A1  - Schmidt, Bernd
A1  - Elizarov, Nelli
A1  - Berger, René
A1  - Hölter, Frank
T1  - Scope and limitations of the Heck–Matsuda-coupling of phenol diazonium salts and styrenes
BT  - a protecting-group economic synthesis of phenolic stilbenes
N2  - 4-Phenol diazonium salts undergo Pd-catalyzed Heck reactions with various styrenes to 4’-hydroxy stilbenes. In almost all cases higher yields and fewer side products were observed, compared to the analogous 4-methoxy benzene diazonium salts. In contrast, the reaction fails completely with 2- and 3-phenol diazonium salts. For these substitution patterns the methoxy-substituted derivatives are superior.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 242 
KW  - catalyzed cross metathesis
KW  - o bond formation
KW  - arenediazonium salts
KW  - stereoselective-synthesis
KW  - arylboronic acids
KW  - substituted stilbenes
KW  - aryldiazonium salts
KW  - palladium catalyst
KW  - trans-stilbenes
KW  - boronic acid
Y1  - 2013
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-95070
SP  - 3674
EP  - 3691
ER  -