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Titlebook: Hydrosilylation; A Comprehensive Revi Bogdan Marciniec Book 2009 Springer Science+Business Media B.V. 2009 Alkenes.Alkynes.Carbon-Carbon mu

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1875-3108 compounds are presented. This monograph shows the extensive development in the application of hydrosilylation in organic and asymmetric syntheses and in polymer and material science..978-90-481-7791-2978-1-4020-8172-9Series ISSN 1875-3108 Series E-ISSN 1875-3086
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Asymmetric Hydrosilylation of Prochiral Alkenes and Their Derivativespresence of rhodium based complexes. Selected processes catalysed by yttrium and lanthanide complexes are also discussed. The chapter ends with brief presentation of some examples of free radical initiated asymmetric hydrosilylation.
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Hydrosilylation of Unsaturated Carbon—Heteroatom Bondsnitiating systems as well as metals (or supported metals) are described. In a separate section, the progress in hydrosilylation of CO. is summarised. Finally, the addition of Si—H to other unsaturated bonds such as C═S, S═O and N═N is shortly described.
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Book 2009n and silicon related compounds. Despite the intensive research and continued interest generated by organosilicon compounds, no comprehensive book incorporating its various aspects has been published this century...The aim of this book is to comprehensively review the advances of hydrosilylation pro
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1875-3108 nistic, structural, and synthetic developments in the field .For fifty years, Hydrosilylation has been one of the most fundamental and elegant methods for the laboratory and industrial synthesis of organosilicon and silicon related compounds. Despite the intensive research and continued interest gen
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Hydrosilylation of Alkenes and Their Derivativese been cited. These catalysts offer many convenient synthetic routes to molecular organosilicon reagents characterised by increased efficiency i.e. the yield and selectivity as well as turnover rate. The choice of catalyst determines the mechanism of catalysis, whose rational development for individual catalytic systems is extensively discussed.
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