4.7 Article

Efficient activation of 2-Iminomethylpyridine/Cobalt-Based alkyne [2+2+2}cycloaddition catalyst by addition of a silver salt

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 349, Issue 14-15, Pages 2368-2374

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200700188

Keywords

catalytic cycloaddition; cobalt; iminomethylpyridine; silver triflate; substituted benzenes

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The addition of silver triflate (AgOTf) or silver hexafluoroantimonate (AgSbF6) significantly increased the activity of the 2-(arylimino)methyl-pyridine/cobalt(II) chloride hexahydrate (COCl2 center dot 6H(2)O)/zinc catalyst in alkyne cyclotrimerizations thereby accelerating the reaction and enabling the use of unactivated, simple internal alkynes as the monoyne substrate: The rate of reaction was found to be highly dependent on the nature of the counter anion (X-) and the ligand (L) in the postulated cationic cobalt(I) complex [LCo(l)]X-+(-).

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