63731-32-8Relevant articles and documents
A direct, copper-catalyzed functionalization of pyridines with alkynes
Beveridge, Ramsay E.,Arndtsen, Bruce A.
experimental part, p. 1000 - 1008 (2010/06/16)
A one-pot, copper-catalyzed method to construct 2-alk-ynylpyridines is presented. This provides a route to access these products directly from terminal alkynes and the parent pyridine, and without prefunctionalization of the pyridine core. In addition, (Z)-alk-2-enylpyridines can be prepared via a related procedure. These reactions are used to synthesize a number of new alkynyl-and alkenyl-substituted pyridines in one pot.
A Novel Ethynylation of Pyridines by Reissert-Henze Type Reaction
Nishiwaki, Nagatoshi,Minakata, Satoshi,Komatsu, Mitsuo,Ohshiro, Yoshiki
, p. 773 - 776 (2007/10/02)
Reaction of N-benzoyloxypyridinium chloride, Reissert-Henze salt, with silver acetylide gave the pyridine ethynylated selectively at 2-position.The reaction is applicable to various substituted pyridines and pyridine homologs.