Applied Homogeneous Catalysis with Organometallic Compounds: by Boy Cornils, Wolfgang A. Herrmann

By Boy Cornils, Wolfgang A. Herrmann

Eventually as softcover: Homogeneous catalysis is the luck tale of organometallic chemistry. because the discovery of hydroformylation via O. Roelen in 1938, catalytic functions have cleared the path of organometallic compounds in undefined. Bulk and nice chemical compounds, or even usual items are being produced through homogeneous organometallic catalysis. the big breadth of this subject in view of either easy study and commercial software is met congenially during this instruction manual edited together by means of W. A. Herrmann (Technical collage Munich) and B. Cornils (Hoechst AG, Frankfurt). The record of over ninety individuals reads like a who-is-who in organometallic chemistry and homogeneous catalysis. during this instruction manual, specialists will locate the present state of the art of their box and complicated scholars will enjoy the concise therapy of vital catalytic reactions and techniques. With its balanced presentation of the really interdisciplinary subject and its striking editor- and authorship, the 'Cornils/Herrmann' is past universal criteria.

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Additional info for Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook in Two Volumes

Example text

While the key synthetic feature is a Wittig-type coupling between vinyl-P-ionone (C,,) and y-formylcrotyl acetate (C,), there is also an earlier hydroformylation step in the synthesis of a precursor compound: 1-vinylethylene diacetate is hydroformylated under high-pressure conditions yielding the brunched aldehyde with regioselectivities up to 80 YO. This intermediate is then transferred into the a$-unsaturated derivative which couples with the C1,-ylide building block to form the Czo-vitaminA according to Scheme 1 [39a-c].

Optionally, these complexes may be modified by ligands (L). A general composition is represented by Structure 1. unmodified”, whereas coordination of the metal center by ligands other than CO or hydrogen are designated “modified”. Various precursor compounds may form the active hydroformylation species under suitable conditions. Even transition metal chlorides are converted to metal carbonyl hydrides under drastic conditions (high pressure and temperature) and in the presence of base. Variation of the Central Atom Monornetallic Catalysts Modern hydroformylation research is almost exclusively focused on four transition metals: cobalt, rhodium, platinum and to considerable extent ruthenium [13].

Mizoroki (1971172): Pd-catal. -D coupling" G. Wilkinson (1965): Rh-phosphine complexes as catalysts E. 0. Fischer (1964): metal-carbenecomplexes F. A. Cotton (1962): metal-metal multiple bonds -. T. H. Coffield (1957): alkyl migration M + CO P. L. Pauson I S . A. g. H. Nozaki, R. Noyori, 8. Sharpless) E. G. Kuntz, B. Cornils (1978): two-phase catalysis (hydroformylation) W. Keim ISHELL (1977): SHOP W. S. Knowles IMONSANTO (1971): L-DOPA R. L. for 0x0 synth. + -r F. E. Paulik, J. F. Roth IMONSANTO (1968): carbonylation of CH30H T.

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