TY  - JOUR
A1  - Schmidt, Bernd
A1  - Geissler, Diana
T1  - Ru- and Pd-Catalysed Synthesis of 2-Arylfurans by One-Flask Heck Arylation/Oxidation
JF  - European journal of organic chemistry
N2  - 2,5-Disubstituted furans were synthesized by one-flask Heck arylation/oxidation sequences. The starting materials are 2-substituted 2,3-dihydrofurans, conveniently available by RCM/isomerization sequences, and arenediazonium salts. These react in ligand-free Heck reactions to afford 2,5-disub-stituted 2,5-dihydrofurans, which are oxidized to the corresponding furans without isolation or intermediate workup. The oxidation is conveniently achieved with chloranil or DDQ, depending on the substrate.
KW  - Diazonium salts
KW  - Palladium
KW  - C-C coupling
KW  - Heck coupling
KW  - Furans
KW  - Oxidation
KW  - Oxygen heterocycles
Y1  - 2011
U6  - https://doi.org/10.1002/ejoc.201100549
SN  - 1434-193X
IS  - 25
SP  - 4814
EP  - 4822
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
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  -