403 related articles for article (PubMed ID: 22853624)
1. A C-H borylation approach to Suzuki-Miyaura coupling of typically unstable 2-heteroaryl and polyfluorophenyl boronates.
Robbins DW; Hartwig JF
Org Lett; 2012 Aug; 14(16):4266-9. PubMed ID: 22853624
[TBL] [Abstract][Full Text] [Related]
2. Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters.
Billingsley K; Buchwald SL
J Am Chem Soc; 2007 Mar; 129(11):3358-66. PubMed ID: 17326639
[TBL] [Abstract][Full Text] [Related]
3. Borylation and silylation of C-H bonds: a platform for diverse C-H bond functionalizations.
Hartwig JF
Acc Chem Res; 2012 Jun; 45(6):864-73. PubMed ID: 22075137
[TBL] [Abstract][Full Text] [Related]
4. One-pot synthesis of arylboronic acids and aryl trifluoroborates by Ir-catalyzed borylation of arenes.
Murphy JM; Tzschucke CC; Hartwig JF
Org Lett; 2007 Mar; 9(5):757-60. PubMed ID: 17274623
[TBL] [Abstract][Full Text] [Related]
5. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.
Kinzel T; Zhang Y; Buchwald SL
J Am Chem Soc; 2010 Oct; 132(40):14073-5. PubMed ID: 20858009
[TBL] [Abstract][Full Text] [Related]
6. Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure.
Barder TE; Walker SD; Martinelli JR; Buchwald SL
J Am Chem Soc; 2005 Apr; 127(13):4685-96. PubMed ID: 15796535
[TBL] [Abstract][Full Text] [Related]
7. A general Suzuki cross-coupling reaction of heteroaromatics catalyzed by nanopalladium on amino-functionalized siliceous mesocellular foam.
Bratt E; Verho O; Johansson MJ; Bäckvall JE
J Org Chem; 2014 May; 79(9):3946-54. PubMed ID: 24673451
[TBL] [Abstract][Full Text] [Related]
8. Sterically controlled iodination of arenes via iridium-catalyzed C-H borylation.
Partridge BM; Hartwig JF
Org Lett; 2013 Jan; 15(1):140-3. PubMed ID: 23256483
[TBL] [Abstract][Full Text] [Related]
9. Preparation and Suzuki-Miyaura coupling reactions of tetrahydropyridine-2-boronic acid pinacol esters.
Occhiato EG; Lo Galbo F; Guarna A
J Org Chem; 2005 Sep; 70(18):7324-30. PubMed ID: 16122254
[TBL] [Abstract][Full Text] [Related]
10. Cross-coupling reaction of saccharide-based alkenyl boronic acids with aryl halides: the synthesis of bergenin.
Parkan K; Pohl R; Kotora M
Chemistry; 2014 Apr; 20(15):4414-9. PubMed ID: 24590755
[TBL] [Abstract][Full Text] [Related]
11. DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions.
Reilly MK; Rychnovsky SD
Synlett; 2011 Oct; 2011(16):. PubMed ID: 24371372
[TBL] [Abstract][Full Text] [Related]
12. One-pot reductive amination and Suzuki-Miyaura cross-coupling of formyl aryl and heteroaryl MIDA boronates in array format.
Grob JE; Nunez J; Dechantsreiter MA; Hamann LG
J Org Chem; 2011 Jun; 76(12):4930-40. PubMed ID: 21526832
[TBL] [Abstract][Full Text] [Related]
13. A modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid.
Molander GA; Trice SL; Tschaen B
Tetrahedron; 2015 Sep; 71(35):5758-5764. PubMed ID: 26257439
[TBL] [Abstract][Full Text] [Related]
14. Iridium-catalyzed C-H borylation of heteroarenes: scope, regioselectivity, application to late-stage functionalization, and mechanism.
Larsen MA; Hartwig JF
J Am Chem Soc; 2014 Mar; 136(11):4287-99. PubMed ID: 24506058
[TBL] [Abstract][Full Text] [Related]
15. Palladium-catalyzed borylation of aryl (pseudo)halides and its applications in biaryl synthesis.
Ji H; Cai J; Gan N; Wang Z; Wu L; Li G; Yi T
Chem Cent J; 2018 Dec; 12(1):136. PubMed ID: 30564982
[TBL] [Abstract][Full Text] [Related]
16. Biaryl synthesis via Pd-catalyzed decarboxylative coupling of aromatic carboxylates with aryl halides.
Goossen LJ; Rodríguez N; Melzer B; Linder C; Deng G; Levy LM
J Am Chem Soc; 2007 Apr; 129(15):4824-33. PubMed ID: 17375927
[TBL] [Abstract][Full Text] [Related]
17. Site-differentiated polyboron arenes prepared by direct C-H borylation and their highly selective Suzuki-Miyaura cross-coupling reactions.
Xu L; Ding S; Li P
Angew Chem Int Ed Engl; 2014 Feb; 53(7):1822-6. PubMed ID: 24505002
[TBL] [Abstract][Full Text] [Related]
18. Palladium membrane-installed microchannel devices for instantaneous Suzuki-Miyaura cross-coupling.
Yamada YM; Watanabe T; Beppu T; Fukuyama N; Torii K; Uozumi Y
Chemistry; 2010 Oct; 16(37):11311-9. PubMed ID: 20715196
[TBL] [Abstract][Full Text] [Related]
19. Micelle-Enabled Suzuki-Miyaura Cross-Coupling of Heteroaryl Boronate Esters.
Guo P; Zhang H; Zhou J; Gallou F; Parmentier M; Wang H
J Org Chem; 2018 Jul; 83(14):7523-7527. PubMed ID: 29799748
[TBL] [Abstract][Full Text] [Related]
20. Palladium-Catalyzed ortho-C-H Arylation of Acetophenone Oxime Ethers with Aryl Pinacol Boronic Esters.
Reddy DM; Wang SC; Du K; Lee CF
J Org Chem; 2017 Oct; 82(19):10070-10076. PubMed ID: 28856888
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]