161 related articles for article (PubMed ID: 18080264)
1. Pd PEPPSI-IPr-mediated reactions in metal-coated capillaries under MACOS: the synthesis of indoles by sequential aryl amination/Heck coupling.
Shore G; Morin S; Mallik D; Organ MG
Chemistry; 2008; 14(4):1351-6. PubMed ID: 18080264
[TBL] [Abstract][Full Text] [Related]
2. Cascade alkenyl amination/Heck reaction promoted by a bifunctional palladium catalyst: a novel one-pot synthesis of indoles from o-haloanilines and alkenyl halides.
Barluenga J; Fernández MA; Aznar F; Valdés C
Chemistry; 2005 Apr; 11(8):2276-83. PubMed ID: 15685588
[TBL] [Abstract][Full Text] [Related]
3. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing.
Glasnov TN; Findenig S; Kappe CO
Chemistry; 2009; 15(4):1001-10. PubMed ID: 19086042
[TBL] [Abstract][Full Text] [Related]
4. Pd on porous glass: a versatile and easily recyclable catalyst for Suzuki and Heck reactions.
Schmöger C; Szuppa T; Tied A; Schneider F; Stolle A; Ondruschka B
ChemSusChem; 2008; 1(4):339-47. PubMed ID: 18605100
[TBL] [Abstract][Full Text] [Related]
5. Genesis of coordinatively unsaturated palladium complexes dissolved from solid precursors during Heck coupling reactions and their role as catalytically active species.
Köhler K; Kleist W; Pröckl SS
Inorg Chem; 2007 Mar; 46(6):1876-83. PubMed ID: 17348718
[TBL] [Abstract][Full Text] [Related]
6. Amination with Pd-NHC complexes: rate and computational studies involving substituted aniline substrates.
Hoi KH; Çalimsiz S; Froese RD; Hopkinson AC; Organ MG
Chemistry; 2012 Jan; 18(1):145-51. PubMed ID: 22139675
[TBL] [Abstract][Full Text] [Related]
7. A microreactor for microwave-assisted capillary (continuous flow) organic synthesis.
Comer E; Organ MG
J Am Chem Soc; 2005 Jun; 127(22):8160-7. PubMed ID: 15926844
[TBL] [Abstract][Full Text] [Related]
8. Diels-Alder cycloadditions by microwave-assisted, continuous flow organic synthesis (MACOS): the role of metal films in the flow tube.
Shore G; Organ MG
Chem Commun (Camb); 2008 Feb; (7):838-40. PubMed ID: 18253521
[TBL] [Abstract][Full Text] [Related]
9. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions.
Marion N; Nolan SP
Acc Chem Res; 2008 Nov; 41(11):1440-9. PubMed ID: 18774825
[TBL] [Abstract][Full Text] [Related]
10. Exploiting noninnocent (E,E)-dibenzylideneacetone (dba) effects in palladium(0)-mediated cross-coupling reactions: modulation of the electronic properties of dba affects catalyst activity and stability in ligand and ligand-free reaction systems.
Fairlamb IJ; Kapdi AR; Lee AF; McGlacken GP; Weissburger F; de Vries AH; Schmieder-van de Vondervoort L
Chemistry; 2006 Nov; 12(34):8750-61. PubMed ID: 16952128
[TBL] [Abstract][Full Text] [Related]
11. A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst.
Organ MG; Avola S; Dubovyk I; Hadei N; Kantchev EA; O'Brien CJ; Valente C
Chemistry; 2006 Jun; 12(18):4749-55. PubMed ID: 16568493
[TBL] [Abstract][Full Text] [Related]
12. Immobilization of palladium in mesoporous silica matrix: preparation, characterization, and its catalytic efficacy in carbon-carbon coupling reactions.
Jana S; Dutta B; Bera R; Koner S
Inorg Chem; 2008 Jun; 47(12):5512-20. PubMed ID: 18459724
[TBL] [Abstract][Full Text] [Related]
13. A highly selective tandem cross-coupling of gem-dihaloolefins for a modular, efficient synthesis of highly functionalized indoles.
Fang YQ; Lautens M
J Org Chem; 2008 Jan; 73(2):538-49. PubMed ID: 18154302
[TBL] [Abstract][Full Text] [Related]
14. Pd-catalyzed aryl amination mediated by well defined, N-heterocyclic carbene (NHC)-Pd precatalysts, PEPPSI.
Organ MG; Abdel-Hadi M; Avola S; Dubovyk I; Hadei N; Kantchev EA; O'Brien CJ; Sayah M; Valente C
Chemistry; 2008; 14(8):2443-52. PubMed ID: 18224651
[TBL] [Abstract][Full Text] [Related]
15. Two flavors of PEPPSI-IPr: activation and diffusion control in a single NHC-ligated Pd catalyst?
Larrosa I; Somoza C; Banquy A; Goldup SM
Org Lett; 2011 Jan; 13(1):146-9. PubMed ID: 21133362
[TBL] [Abstract][Full Text] [Related]
16. Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations.
Baxendale IR; Griffiths-Jones CM; Ley SV; Tranmer GK
Chemistry; 2006 May; 12(16):4407-16. PubMed ID: 16586523
[TBL] [Abstract][Full Text] [Related]
17. Regio- and stereo-selective synthesis of aryl 2-deoxy-C-glycopyranosides by palladium-catalyzed Heck coupling reactions of glycals and aryl iodides.
Li HH; Ye XS
Org Biomol Chem; 2009 Sep; 7(18):3855-61. PubMed ID: 19707693
[TBL] [Abstract][Full Text] [Related]
18. Catalytic sequential reactions involving palladacycle-directed aryl coupling steps.
Catellani M; Motti E; Della Ca' N
Acc Chem Res; 2008 Nov; 41(11):1512-22. PubMed ID: 18680317
[TBL] [Abstract][Full Text] [Related]
19. Biaryls made easy: PEPPSI and the Kumada-Tamao-Corriu reaction.
Organ MG; Abdel-Hadi M; Avola S; Hadei N; Nasielski J; O'brien CJ; Valente C
Chemistry; 2007; 13(1):150-7. PubMed ID: 17143919
[TBL] [Abstract][Full Text] [Related]
20. Rationally designed pincer-type heck catalysts bearing aminophosphine substituents: Pd IV intermediates and palladium nanoparticles.
Bolliger JL; Blacque O; Frech CM
Chemistry; 2008; 14(26):7969-77. PubMed ID: 18618875
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
