51770-89-9Relevant articles and documents
Stille cross-couplings of unactivated secondary alkyl halides using monoorganotin reagents
Powell, David A.,Maki, Toshihide,Fu, Gregory C.
, p. 510 - 511 (2005)
The first catalyst that achieves Stille cross-couplings of secondary (as well as primary) alkyl halides has been developed. The method employs easily handled and inexpensive catalyst components (NiCl2 and 2,2′-bipyridine) and, through the use of monoorganotin reagents, avoids the formation of toxic and difficult-to-remove triorganotin side products. Copyright
