Zobrazeno 1 - 10
of 152
pro vyhledávání: '"John F, Bower"'
Publikováno v:
Cadge, J A, Gates, P J, Bower, J F & Russell, C A 2022, ' Migratory Insertion of CO into a Au-C Bond ', Journal of the American Chemical Society, vol. 144, no. 43, pp. 19719-19725 . https://doi.org/10.1021/jacs.2c10432
A MeDalPhos-ligated gold(III) metallafluorene complex, generated via C-C oxidative addition of biphenylene, reacts with CO to produce 9-fluorenone. Experimental and computational studies show that this proceeds via a hitherto unknown migratory insert
Publikováno v:
Journal of the American Chemical Society
Unique examples of aza-Heck-based C(sp3)-H functionalization cascades are described. Under Pd(0)-catalyzed conditions, the aza-Heck-type cyclization of N-(pentafluorobenzoyloxy)carbamates generates alkyl-Pd(II) intermediates that effect C(sp3)-H pall
Publikováno v:
Angewandte Chemie International Edition. 62
Publikováno v:
Journal of the American Chemical Society. 144:11069-11074
Under Rh-catalyzed conditions, secondary amines and anilines function as directing groups to facilitate regioselective C-C bond activation of nonactivated cyclopropanes. The resulting amino-stabilized rhodacycles undergo carbonylative C-N bond format
Autor:
Andrew G. Dalling, John F. Bower
Publikováno v:
CHIMIA, Vol 72, Iss 9 (2018)
This review concentrates on recent developments from our laboratory concerning the Rh-catalyzed carbonylative C–C bond activation of cyclopropanes. Specifically, we have found that N-based directing groups are effective at controlling the regiosele
Externí odkaz:
https://doaj.org/article/3383f92f6a8a4147a5e98693d93339e8
Autor:
Phillippa Cooper, Andrew G. Dalling, Elliot H. E. Farrar, Timothy P. Aldhous, Simon Grélaud, Eleanor Lester, Lyman J. Feron, Paul D. Kemmitt, Matthew N. Grayson, John F. Bower
Publikováno v:
Cooper, P, Dalling, A G, Farrar, E H E, Aldhous, T P, Grélaud, S, Lester, E, Feron, L J, Kemmitt, P D, Grayson, M N & Bower, J F 2022, ' Atom and step economical synthesis of acyclic quaternary centers via iridium-catalyzed hydroarylative cross-coupling of 1,1-disubstituted alkenes ', Chemical Science, vol. 13, no. 37, pp. 11183-11189 . https://doi.org/10.1039/D2SC02790A
Quaternary benzylic centers are accessed with high atom and step economy by Ir-catalyzed alkene hydroarylation. These studies provide unique examples of the use of non-polarized 1,1-disubstituted alkenes in branch selective Murai-type hydro(hetero)ar
Autor:
Guilherme A. M. Jardim, Renato L. de Carvalho, Mateus P. Nunes, Luana A. Machado, Leandro D. Almeida, Karim A. Bahou, John F. Bower, Eufrânio N. da Silva Júnior
Publikováno v:
Chemical Communications
Metal catalyzed C-H functionalization offers a versatile platform for methodology development and a wide variety of reactions now exist for the chemo- and site-selective functionalization of organic molecules. Cyclopentadienyl-metal (CpM) complexes o
Publikováno v:
Synlett.
Catalytic processes involving oxidative addition of a C–C bond to a transition metal allow the atom economical assembly of complex scaffolds. The focus of this Account is on C–C bond activation-based methodologies that employ minimally activated
Publikováno v:
Angewandte Chemie International Edition. 60:24976-24983
A combined theoretical and experimental approach has been used to study the unusual mechanism of oxidative addition of aryl iodides to [bipyAu(C2 H4 )]+ complexes. The modular nature of this system allowed a systematic assessment of the effects of co
Publikováno v:
Journal of the American Chemical Society. 144(37)
Unique examples of aza-Heck-based C(sp