Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 46, Pages 6194-6196Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b815665d
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Using density functional theory with the B3LYP and M06 functionals, we show conclusively that the (H(2)IMes)(Cl)(2)Ru olefin metathesis mechanism is bottom-bound with the chlorides remaining trans throughout the reaction, thus attempts to effect diastereo- and enantioselectivity should focus on manipulations that maintain the trans-dichloro Ru geometry.
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