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 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.
1101668771
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 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.
379.99 In Stock
Metal Catalyzed Reductive C-C Bond Formation: A Departure from Preformed Organometallic Reagents

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

by Michael J Krische (Editor)
Metal Catalyzed Reductive C-C Bond Formation: A Departure from Preformed Organometallic Reagents

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

by Michael J Krische (Editor)

Hardcover(2007)

$379.99 
  • SHIP THIS ITEM
    In stock. Ships in 1-2 days.
  • PICK UP IN STORE

    Your local store may have stock of this item.

Related collections and offers


Overview

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.

Product Details

ISBN-13: 9783540728788
Publisher: Springer Berlin Heidelberg
Publication date: 08/23/2007
Series: Topics in Current Chemistry , #279
Edition description: 2007
Pages: 264
Product dimensions: 6.10(w) x 9.25(h) x (d)

Table of Contents

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.
From the B&N Reads Blog

Customer Reviews