Some scientific research about 172222-30-9

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Ruthenium-catalyzed ring-closing metathesis on alkene-tethered Fischer carbene complexes

Alkene-terminated tethers have been assembled around a Fischer carbene moiety by C-alkylation of the alpha-carbon or N-alkylation of amino carbene complexes by a phase-transfer catalyzed procedure developed in this laboratory. Small or medium-sized, pendant, fused or spirocyclic rings have then been formed by ring-closing metathesis involving such substrates in good to excellent yields. By engaging one of the allyl tethers of a diallylamino group as a ligand for the metal center, it is possible to dictate the direction of cyclization by metathesis.

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Reference£º
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI