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...

全面介紹

Enregistré dans:
書目詳細資料
主要作者: Krische, Michael J. (Éditeur intellectuel)
格式: Livre numérique
語言:Anglais
出版: Berlin, Heidelberg : Springer Berlin Heidelberg [20..].
Cham : Springer Nature
版:1st ed. 2007.
叢編:Topics in Current Chemistry 279
主題:
在線閱讀:Accès sur la plateforme de l'éditeur
Accès sur la plateforme Istex
Accès Université d'Orléans
Accès INSA CVL
提示: Archives Springer e-books (Licence nationale)
Archives Springer e-books (Licence nationale)
Autres localisations: Voir dans le Sudoc
Variante du titre:With contributions by numerous experts
Edition sous un autre format:• Metal catalyzed reductive C-C bond formation, a departure from preformed organometallic reagents, Volume editor : Michael J. Krische, Berlin, Springer, 2007, 1 vol. (X-264 p.), Topics in current chemistry, 978-3-540-72878-8
• Metal Catalyzed Reductive C-C Bond Formation, Texte imprimé, 9783642091988
• Metal Catalyzed Reductive C-C Bond Formation, Texte imprimé, 9783540839095
LEADER 05013nam a22004577a 4500
001 939358
008 080410q2000 xx ||| |||| 00| 0 eng d
009 PPN123162742
020 |a 9783540728795 
041 0 |a eng 
082 |a 547 
082 |a 540 
100 1 |a Krische, Michael J. 
240 1 0 |a With contributions by numerous experts 
245 1 0 |a Metal Catalyzed Reductive C-C Bond Formation :  |b A Departure from Preformed Organometallic Reagents   |c edited by Michael J. Krische. 
250 |a 1st ed. 2007. 
260 |a Berlin, Heidelberg :  |b Springer Berlin Heidelberg. 
260 |a Cham :  |b Springer Nature,  |c [20..]. 
490 0 |a Topics in Current Chemistry  |v 279  |x 1436-5049 
500 |a Archives Springer e-books (Licence nationale) 
500 |a Archives Springer e-books (Licence nationale) 
505 1 |a 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 
506 |a Accès en ligne pour les établissements français bénéficiaires des licences nationales 
506 |a Accès soumis à abonnement pour tout autre établissement 
506 |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 
520 |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 
650 |a Chimie organométallique 
650 |a Chimie 
650 |a Composés organiques 
650 |a Chimie organique 
650 |a Catalyseurs métalliques 
650 |a Liaisons carbone-carbone 
700 1 |a Krische, Michael J.  |4 edt 
776 0 |0 119697629  |t Metal catalyzed reductive C-C bond formation  |o a departure from preformed organometallic reagents  |f Volume editor : Michael J. Krische  |c Berlin  |n Springer  |d 2007  |p 1 vol. (X-264 p.)  |s Topics in current chemistry  |z 978-3-540-72878-8 
776 0 |t Metal Catalyzed Reductive C-C Bond Formation  |b Texte imprimé  |z 9783642091988 
776 0 |t Metal Catalyzed Reductive C-C Bond Formation  |b Texte imprimé  |z 9783540839095 
856 4 |q PDF  |u https://doi.org/10.1007/978-3-540-72879-5  |z Accès sur la plateforme de l'éditeur 
856 4 |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-1VQF40CQ-X  |z Accès sur la plateforme Istex 
856 4 |5 452349901:747882894  |u https://ezproxy.univ-orleans.fr/login?url=https://dx.doi.org/10.1007/978-3-540-72879-5  |z Accès Université d'Orléans 
856 4 |5 180339901:750895535  |u https://ezproxy.insa-cvl.fr/login?qurl=https://dx.doi.org/10.1007/978-3-540-72879-5  |z Accès INSA CVL 
997 |0 939358  |1 Livre numérique  |a Ressource numérique  |b INSA  |b ENSA  |c 0/Bibliothèque numérique/  |c 1/Bibliothèque numérique/Autre ressource numérique/