TY - JOUR
T1 - Synthesis of 2,2'-bipyridines : from versatile building blocks to sexy architectures and functional (nano)materials
AU - Newkome, G.R.
AU - Patri, A.K.
AU - Holder, E.
AU - Schubert, U.S.
PY - 2004
Y1 - 2004
N2 - The latest synthetic strategies to prepare 2,2-bipyridine and its mono-substituted, symmetrical and unsymmetrical 3,3-, 4,4-, 5,5-, and 6,6-disubstituted derivatives are critically discussed and evaluated. Different coupling procedures to achieve new symmetrical and unsymmetrical functionalized 2,2-bipyridines, such as Stille-type, Negishi-type, and Suzuki-type cross-coupling reactions are discussed in detail. Moreover, condensation procedures that allow further variations are presented. The application of functional group transformations for access to additional groups is examined.
AB - The latest synthetic strategies to prepare 2,2-bipyridine and its mono-substituted, symmetrical and unsymmetrical 3,3-, 4,4-, 5,5-, and 6,6-disubstituted derivatives are critically discussed and evaluated. Different coupling procedures to achieve new symmetrical and unsymmetrical functionalized 2,2-bipyridines, such as Stille-type, Negishi-type, and Suzuki-type cross-coupling reactions are discussed in detail. Moreover, condensation procedures that allow further variations are presented. The application of functional group transformations for access to additional groups is examined.
U2 - 10.1002/ejoc.200300399
DO - 10.1002/ejoc.200300399
M3 - Article
VL - 2004
SP - 235
EP - 254
JO - European Journal of Organic Chemistry
JF - European Journal of Organic Chemistry
SN - 1434-193X
IS - 2
ER -