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- W2013715079 abstract "Abstract CpCo I ‐olefin‐phosphite and CpCo I ‐bisphosphite complexes were systematically prepared and their reactivity in [2+2+2] cycloaddition reactions compared with highly active [CpCo(H 2 CCHSiMe 3 ) 2 ] ( 1 ). Whereas 1 is an excellent precursor for the synthesis of [CpCo(olefin)(phosphite)] complexes ( 2 a – f ), [CpCo(phosphite) 2 ] complexes ( 3 a – e ) were prepared photochemically from [CpCo(cod)]. The complexes were evaluated in the cyclotrimerization reaction of diynes with nitriles yielding pyridines. For [CpCo(olefin)(phosphite)], as well as some of the [CpCo(phosphite) 2 ] complexes, reaction temperatures as low as 50 °C were sufficient to perform the cycloaddition reaction. A direct comparison showed that the order of reactivity for the complex ligands was olefin 2 >olefin/phosphite>phosphites 2 . The complexes with mixed ligands favorably combine reactivity and stability. Calculations on the ligand dissociation from [CpCo(olefin)(phosphite)] proved that the phosphite is dissociating before the olefin. [CpCo(H 2 CCHSiMe 3 ){P(OPh) 3 }] ( 2 a ) was investigated for the co‐cyclization of diynes and nitriles and found to be an efficient catalyst at rather mild temperatures." @default.
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- W2013715079 date "2012-12-18" @default.
- W2013715079 modified "2023-10-18" @default.
- W2013715079 title "Fine-Tuning the Reactivity and Stability by Systematic Ligand Variations in CpCo<sup>I</sup>Complexes as Catalysts for [2+2+2] Cycloaddition Reactions" @default.
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- W2013715079 doi "https://doi.org/10.1002/chem.201202946" @default.
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