Metal Catalyzed Reductive C-C Bond Formation : A Departure from Preformed Organometallic Reagents

TheprototypicalcatalyticreductiveC Cbondformations,theFischer-Tropsch reaction [1] and alkene hydroformylation [2], were discovered in 1922 and 1938, respectively [3,4]. These processes, which involve reductive coupling to carbon monoxide, have long been applied to the industrial manufacture of comm...

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Auteur principal : Krische Michael J (Éditeur scientifique)
Format : Livre
Langue : anglais
Titre complet : Metal Catalyzed Reductive C-C Bond Formation : A Departure from Preformed Organometallic Reagents / edited by Michael J. Krische.
Édition : 1st ed. 2007.
Publié : Berlin, Heidelberg : Springer Berlin Heidelberg , [20..]
Cham : Springer Nature
Collection : Topics in current chemistry (Internet) ; 279
Accès en ligne : Accès Nantes Université
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Condition d'utilisation et de reproduction : Conditions particulières de réutilisation pour les bénéficiaires des licences nationales : https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017
Contenu : Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes. Reductive C C Bond Formation after Epoxide Opening via Electron Transfer. Catalytic Reductive Coupling of Carbonyl Compounds The Pinacol Coupling Reaction and Beyond. Catalytic Reductive Coupling of Alkenes and Alkynes to Carbonyl Compounds and Imines Mediated by Hydrogen. Reductive Aldol, Michael, and Mannich Reactions. Recent Advances in Alkene Hydroformylation. Nickel-Catalyzed Reductive Coupling of Dienes and Carbonyl Compounds. Reductive Coupling of Unactivated Alkenes and Alkynes
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Documents associés : Autre format: Metal catalyzed reductive C-C bond formation
Autre format: Metal Catalyzed Reductive C-C Bond Formation
Autre format: Metal Catalyzed Reductive C-C Bond Formation
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225 0 |a Topics in Current Chemistry  |x 1436-5049  |v 279 
327 1 |a Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes  |a Reductive C C Bond Formation after Epoxide Opening via Electron Transfer  |a Catalytic Reductive Coupling of Carbonyl Compounds The Pinacol Coupling Reaction and Beyond  |a Catalytic Reductive Coupling of Alkenes and Alkynes to Carbonyl Compounds and Imines Mediated by Hydrogen  |a Reductive Aldol, Michael, and Mannich Reactions  |a Recent Advances in Alkene Hydroformylation  |a Nickel-Catalyzed Reductive Coupling of Dienes and Carbonyl Compounds  |a Reductive Coupling of Unactivated Alkenes and Alkynes 
330 |a TheprototypicalcatalyticreductiveC Cbondformations,theFischer-Tropsch reaction [1] and alkene hydroformylation [2], were discovered in 1922 and 1938, respectively [3,4]. These processes, which involve reductive coupling to carbon monoxide, have long been applied to the industrial manufacture of commodity chemicals [5]. Notably, alkene hydroformylation, also known as the oxo-synthesis, has emerged as the largest volume application of homo- neous metal catalysis, accounting for the production of over 7 million metric tons of aldehyde annually. Despite the impact of these prototypical reductive C C bond formations, this ?eld of research lay fallow for several decades. Eventually, the increased availability of mild terminal reductants, in part- ular silanes, led to a renaissance in the area of catalytic reductive C C bond formation.Forexample,the?rstcatalyticreductiveC Ccouplingsbeyond- droformylation, which involve the hydrosilylative dimerization of conjugated dienes [6 12], appeared in 1969 approximately 16 years after the ?rst - ported metal-catalyzed alkene hydrosilylation [13]. Following these seminal studies, the ?eld of catalytic reductive C C bond formation underwent exp- sivegrowth,culminatingintheemergenceofanevergrowingbodyofresearch encompassing a powerful set of transformations. To our knowledge, no thematic volumes devoted solely to metal-catalyzed reductive C C bond formationhave been assembled. For the ?rst time, in this issue of Topics in Current Chemistry,wepresent acompilation ofmonographs from several leaders in this burgeoning area of research. This collection of reviews serves to capture the diversity of catalytic reductive C C couplings presently available and, in turn, the remarkable range of reactivity embodied by such transformations. There is no indication that this ?eld has reached its zenithanditisthehopeofthepresentauthorthatthisvolumewillfuelfurther progress 
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