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Titlebook: Advances in Metal Carbene Chemistry; U. Schubert Book 1989 Kluwer Academic Publishers 1989 ITIES.Ion.Organometallic chemistry.Ruthenium.ca

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Beatriz Andres,Raul Poler,Raquel Sanchis with SMe. cations to yield first η.-thiocarbene complexes and then dithiatungstabicyclo[1.1.0]butane complexes. Comparable η.-phosphinocarbene complexes are obtained on mild thermolysis of tungstaphosphabicyclo[1.1.0]-butanone cations.
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Dario Antonelli,Sergey Astanin,Giulia Brunoum complex (1); oxidation of (3a-f) with Ce. leads to the corresponding γ-lactones. The extension of the above reactions to oxetane allowed the synthesis of the new pentacarbonyl(2-oxacyclohexylidene)chromium complex. It is noteworthy that the oxetane ring opening occurs only in the presence of BF..Et.0.
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Collaboration in a Hyperconnected Worldel synthesis of vinylidene complexes involves reaction of 1-halogeno-l-silylalkenes with unsaturated metal fragments. In the latter reaction butatriene complexes are formed instead, if an excess of alkene is used. On grounds of model reactions, a possible mechanism for the coupling of two vinylidene units is discussed.
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Collaboration in a Hyperconnected World of CpMo(SnPh.) (=CHPh) (CO). migrates to the alkylidene forming an η.-benzyl complex. We conclude that a number of X to carbene or alkylidene migrations proceed at rates suitable for an extensive general study of the phenomenon.
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