258 related articles for article (PubMed ID: 19405470)
1. 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]
2. 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]
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. 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]
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. 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]
7. 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]
8. 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]
9. From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks.
Li J; Grillo AS; Burke MD
Acc Chem Res; 2015 Aug; 48(8):2297-307. PubMed ID: 26200460
[TBL] [Abstract][Full Text] [Related]
10. Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks.
Li J; Burke MD
J Am Chem Soc; 2011 Sep; 133(35):13774-7. PubMed ID: 21823591
[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. 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]
13. 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]
14. Hydrogean Peroxide Inducible Acid-Activatable Prodrug for Targeted Cancer Treatment.
Liu J; Wang J; Si S; Xu J; Xue P
ChemMedChem; 2021 Oct; 16(20):3231-3235. PubMed ID: 34288492
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Radical Instability in Aid of Efficiency: A Powerful Route to Highly Functional MIDA Boronates.
Quiclet-Sire B; Zard SZ
J Am Chem Soc; 2015 Jun; 137(21):6762-5. PubMed ID: 25984592
[TBL] [Abstract][Full Text] [Related]
17. MIDA boronates are hydrolysed fast and slow by two different mechanisms.
Gonzalez JA; Ogba OM; Morehouse GF; Rosson N; Houk KN; Leach AG; Cheong PH; Burke MD; Lloyd-Jones GC
Nat Chem; 2016 Nov; 8(11):1067-1075. PubMed ID: 27768100
[TBL] [Abstract][Full Text] [Related]
18. Palladium-catalyzed cross-coupling reactions of aryl boronic acids with aryl halides in water.
Wang S; Zhang Z; Hu Z; Wang Y; Lei P; Chi H
J Environ Sci (China); 2009; 21 Suppl 1():S124-6. PubMed ID: 25084408
[TBL] [Abstract][Full Text] [Related]
19. Suzuki-Miyaura coupling of heteroaryl boronic acids and vinyl chlorides.
Thakur A; Zhang K; Louie J
Chem Commun (Camb); 2012 Jan; 48(2):203-5. PubMed ID: 22083103
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
