169 related articles for article (PubMed ID: 24224801)
1. Transforming Suzuki-Miyaura cross-couplings of MIDA boronates into a green technology: no organic solvents.
Isley NA; Gallou F; Lipshutz BH
J Am Chem Soc; 2013 Nov; 135(47):17707-10. PubMed ID: 24224801
[TBL] [Abstract][Full Text] [Related]
2. Regioselective synthesis and slow-release Suzuki-Miyaura cross-coupling of MIDA boronate-functionalized isoxazoles and triazoles.
Grob JE; Nunez J; Dechantsreiter MA; Hamann LG
J Org Chem; 2011 Dec; 76(24):10241-8. PubMed ID: 22047083
[TBL] [Abstract][Full Text] [Related]
3. Recent advances in the synthesis and reactivity of MIDA boronates.
Aich D; Kumar P; Ghorai D; Kanti Das K; Panda S
Chem Commun (Camb); 2022 Dec; 58(96):13298-13316. PubMed ID: 36382511
[TBL] [Abstract][Full Text] [Related]
4. A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.
Knapp DM; Gillis EP; Burke MD
J Am Chem Soc; 2009 May; 131(20):6961-3. PubMed ID: 19405470
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Multistep synthesis of complex boronic acids from simple MIDA boronates.
Gillis EP; Burke MD
J Am Chem Soc; 2008 Oct; 130(43):14084-5. PubMed ID: 18837550
[TBL] [Abstract][Full Text] [Related]
7. Nanonickel-catalyzed Suzuki-Miyaura cross-couplings in water.
Handa S; Slack ED; Lipshutz BH
Angew Chem Int Ed Engl; 2015 Oct; 54(41):11994-8. PubMed ID: 26305994
[TBL] [Abstract][Full Text] [Related]
8. Vibrational spectroscopy of N-methyliminodiacetic acid (MIDA)-protected boronate ester: examination of the B-N dative bond.
Reinemann DN; Wright AM; Wolfe JD; Tschumper GS; Hammer NI
J Phys Chem A; 2011 Jun; 115(24):6426-31. PubMed ID: 21557585
[TBL] [Abstract][Full Text] [Related]
9. One-pot C-N/C-C cross-coupling of methyliminodiacetic acid boronyl arenes enabled by protective enolization.
Grob JE; Dechantsreiter MA; Tichkule RB; Connolly MK; Honda A; Tomlinson RC; Hamann LG
Org Lett; 2012 Nov; 14(21):5578-81. PubMed ID: 23092156
[TBL] [Abstract][Full Text] [Related]
10. A Mild Method for Making MIDA Boronates.
Kelly AM; Chen PJ; Klubnick J; Blair DJ; Burke MD
Org Lett; 2020 Dec; 22(24):9408-9414. PubMed ID: 32841037
[TBL] [Abstract][Full Text] [Related]
11. Asymmetric Rh(I)-catalyzed addition of MIDA boronates to N-tert-butanesulfinyl aldimines: development and comparison to trifluoroborates.
Brak K; Ellman JA
J Org Chem; 2010 May; 75(9):3147-50. PubMed ID: 20387846
[TBL] [Abstract][Full Text] [Related]
12. Efficient Suzuki-Miyaura coupling of (hetero)aryl chlorides with thiophene- and furanboronic acids in aqueous n-butanol.
Fleckenstein CA; Plenio H
J Org Chem; 2008 Apr; 73(8):3236-44. PubMed ID: 18355081
[TBL] [Abstract][Full Text] [Related]
13. General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates.
Dick GR; Knapp DM; Gillis EP; Burke MD
Org Lett; 2010 May; 12(10):2314-7. PubMed ID: 20465293
[TBL] [Abstract][Full Text] [Related]
14. Speciation control during Suzuki-Miyaura cross-coupling of haloaryl and haloalkenyl MIDA boronic esters.
Fyfe JW; Valverde E; Seath CP; Kennedy AR; Redmond JM; Anderson NA; Watson AJ
Chemistry; 2015 Jun; 21(24):8951-64. PubMed ID: 25959852
[TBL] [Abstract][Full Text] [Related]
15. Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar catalysis.
Lipshutz BH; Taft BR; Abela AR; Ghorai S; Krasovskiy A; Duplais C
Platin Met Rev; 2012 Apr; 56(2):62-74. PubMed ID: 23555153
[TBL] [Abstract][Full Text] [Related]
16. Copper-facilitated Suzuki reactions: application to 2-heterocyclic boronates.
Deng JZ; Paone DV; Ginnetti AT; Kurihara H; Dreher SD; Weissman SA; Stauffer SR; Burgey CS
Org Lett; 2009 Jan; 11(2):345-7. PubMed ID: 19093828
[TBL] [Abstract][Full Text] [Related]
17. Suzuki-Miyaura cross-coupling reactions in aqueous media: green and sustainable syntheses of biaryls.
Polshettiwar V; Decottignies A; Len C; Fihri A
ChemSusChem; 2010 May; 3(5):502-22. PubMed ID: 20191633
[TBL] [Abstract][Full Text] [Related]
18. On the way towards greener transition-metal-catalyzed processes as quantified by E factors.
Lipshutz BH; Isley NA; Fennewald JC; Slack ED
Angew Chem Int Ed Engl; 2013 Oct; 52(42):10952-8. PubMed ID: 24030905
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of trans-2-(trifluoromethyl)cyclopropanes via Suzuki reactions with an N-methyliminodiacetic acid boronate.
Duncton MA; Singh R
Org Lett; 2013 Sep; 15(17):4284-7. PubMed ID: 23952128
[TBL] [Abstract][Full Text] [Related]
20. Palladium-catalyzed Suzuki-Miyaura cross-couplings of stable glycal boronates for robust synthesis of C-1 glycals.
Chen A; Han Y; Wu R; Yang B; Zhu L; Zhu F
Nat Commun; 2024 Jun; 15(1):5228. PubMed ID: 38898022
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
