Titlebook: Carbonylation; Direct Synthesis of H. M. Colquhoun,D. J. Thompson,M. V. Twigg Book 1991 Springer Science+Business Media New York 1991 ITIE

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Bifurcations and Routes to Chaos,equipment is only occasionally required and there is rarely any need for the extremes of pressure and temperature synonymous with older industrial carbonylation processes. Small-scale atmospheric pressure procedures can in fact often be carried out in conventional laboratory glassware. In procedural

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Pattern Formation and Spatiotemporal Chaos,ntrinsic value of aldehydes as synthetic intermediates but also the scarcity of truly general routes to aldehydes themselves. As a result, a great number of relatively specific syntheses have been devised, often relying on partial oxidation or reduction procedures in which the danger of overreaction

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Linear and Nonlinear Dispersive Waves,vious difference that a carbanion or carbonium ion source is now required in place of a hydride or proton donor. Favored starting materials are again halocarbons, alkenes, or alkynes, which are readily carbonylated to a range of symmetrical, unsymmetrical, or cyclic ketones. For example, one of the

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https://doi.org/10.1007/978-3-642-12799-1other carboxylic acid derivatives. Included here are amides, anhydrides, acyl halides, urethanes, ureas, and isocyanates. The last three types of compound can be viewed, respectively, as the products of esterification, amidation, and dehydration of carbamic acids (RNHCOOH), and carbonylative synthes

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