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An efficient [4 + 2 + 1] entry to seven-membered rings
Authors:Ni Yike  Montgomery John
Institution:Department of Chemistry, Wayne State University, Detroit, Michigan 48202, USA.
Abstract:A new nickel-catalyzed procedure for the 4 + 2 + 1] cycloaddition of trimethylsilyl diazomethane with alkynes tethered to dienes has been developed. A broad range of unsaturated substrates participate in the sequence, and stereoselectivities are generally excellent. Three possible mechanisms are proposed, and each involves the generation of a transient nickel carbene species.
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