“…Driven by the favourable binding enthalpy of Si–N, 17 a σ-bond metathesis took place via a four-membered ring transition state ( B ) to form intermediate C and 1-(trimethylsilyl)-1 H -benzotriazole ( D ). 18 Finally, C underwent reductive elimination to release the β-chloro esters ( 3 ) and regenerated Ni(0).…”
Ni-catalyzed cross-coupling of N-acyl benzotriazoles, oxiranes/oxetanes and trimethylsilyl halides afforded β- and γ-halo esters with good yields and wide substrate scope. Preliminary mechanistic studies point to a σ-bond metathesis pathway.
“…Driven by the favourable binding enthalpy of Si–N, 17 a σ-bond metathesis took place via a four-membered ring transition state ( B ) to form intermediate C and 1-(trimethylsilyl)-1 H -benzotriazole ( D ). 18 Finally, C underwent reductive elimination to release the β-chloro esters ( 3 ) and regenerated Ni(0).…”
Ni-catalyzed cross-coupling of N-acyl benzotriazoles, oxiranes/oxetanes and trimethylsilyl halides afforded β- and γ-halo esters with good yields and wide substrate scope. Preliminary mechanistic studies point to a σ-bond metathesis pathway.
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