2002
DOI: 10.1016/s0022-328x(02)01881-8
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Synthesis of bis-oxazoline-ruthenium(II)-arene complexes.

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Cited by 55 publications
(30 citation statements)
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“…Starting from these observations, variations on the catalytic system and especially the use of bidentate ligands such as bisbenzoxazole, [16] chiral bisoxazoline and diimine, [17] associated with a ruthenium source, have shown isomerisation capability. The most efficient catalytic system B was then evaluated for terpenoids.…”
Section: Resultsmentioning
confidence: 99%
“…Starting from these observations, variations on the catalytic system and especially the use of bidentate ligands such as bisbenzoxazole, [16] chiral bisoxazoline and diimine, [17] associated with a ruthenium source, have shown isomerisation capability. The most efficient catalytic system B was then evaluated for terpenoids.…”
Section: Resultsmentioning
confidence: 99%
“…[1] Especially, a variety of RuX 2 (arene)(L) complexes promoting catalytic reactions such as nucleophilic addition to triple bonds to form furans (L ϭ imidazoline, tetrahydropyrimidine, [2] benzimidazole [3] ), hydrogen transfer (L ϭ amino acid, [4] amino alcohol, [5] diamine [6] ), cyclopropanation (L ϭ diamine [7] ), or DielsϪAlder cycloaddition and Claisen rearrangement [L ϭ bis(oxazoline) [8,9] ]. It is also well established that RuCl 2 (arene)(L) complexes can easily be transformed by activation of propargylic alcohols into cationic ruthenium(allenylidene) complexes, which have shown catalytic properties in olefin metathesis.…”
Section: Introductionmentioning
confidence: 99%
“…Scheme 8 The bis(oxazoline) 17 was then used to prepare a welldefined ruthenium() (arene) complex according to the procedure we previously used for achiral bis(oxazoline)ruthenium complexes. [17] Two equiv. of the bis(oxazoline) 17 were reacted with the ruthenium complex [RuCl 2 (p-cymene)] 2 in methanol at room temperature with two equiv.…”
Section: Bis(oxazoline) Ruthenium Precursorsmentioning
confidence: 99%
“…Since well-defined chelating dinitrogen containing ruthenium complexes of type [RuCl{bis(oxazoline)}(arene)] ϩ X Ϫ have already shown some activity for this reaction, [17] we have explored the catalyst modification based on [Ru 3 (CO) 12 ], as a ruthenium source, by replacing the bulky imidazolinylidene precursor by a sterically hindered diimine or bis(oxazoline)ligand.…”
Section: Use Of Dinitrogen Chelating Ligands In Ruthenium Catalyst Prmentioning
confidence: 99%