Ruthenium-Catalyzed [1,n]-Metallotropic Shift (n = 3, 5) of Alkynyl Carbene Complex Intermediates
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文摘
The ruthenium-catalyzed isomerization of diynes and triynes involving propargyl carboxylate moieties affords dienynes and dienediynes, respectively. The [1,n]-metallotropic shift (n = 3, 5) (carbene walk) of in situ generated alkynyl carbene complexes has been proposed for the catalytic isomerization reaction.

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