Liu Y, Zhang X, Li J, Pei X, Pang S, He C
JACS Au. 2025; 5(2):990-997.
PMID: 40017768
PMC: 11862949.
DOI: 10.1021/jacsau.4c01239.
Li J, Li G, Tsang S
Acc Chem Res. 2025; 58(4):555-569.
PMID: 39873634
PMC: 11840930.
DOI: 10.1021/acs.accounts.4c00683.
Yamamoto Y, Konakazawa Y, Fujiwara K, Ogawa A
Beilstein J Org Chem. 2024; 20:2577-2584.
PMID: 39403306
PMC: 11472659.
DOI: 10.3762/bjoc.20.216.
Dai C, Xu J, Xu X, Wang C, You T, Li W
JACS Au. 2024; 4(8):3183-3193.
PMID: 39211611
PMC: 11350594.
DOI: 10.1021/jacsau.4c00492.
Kang S, Lv J, Wang T, Wu B, Wang M, Shi Z
Nat Commun. 2024; 15(1):7380.
PMID: 39191737
PMC: 11350172.
DOI: 10.1038/s41467-024-51484-6.
Transition Metal Mimetic π-Activation by Cationic Bismuth(III) Catalysts for Allylic C-H Functionalization of Olefins Using C═O and C═N Electrophiles.
Wang R, Martinez S, Schwarzmann J, Zhao C, Ramler J, Lichtenberg C
J Am Chem Soc. 2024; 146(32):22122-22128.
PMID: 39102739
PMC: 11328129.
DOI: 10.1021/jacs.4c06235.
Engineering Frustrated Lewis Pair Active Sites in Porous Organic Scaffolds for Catalytic CO Hydrogenation.
Das S, Laplaza R, Blaskovits J, Corminboeuf C
J Am Chem Soc. 2024; 146(23):15806-15814.
PMID: 38814248
PMC: 11177311.
DOI: 10.1021/jacs.4c01890.
Tunable molecular editing of indoles with fluoroalkyl carbenes.
Liu S, Yang Y, Song Q, Liu Z, Lu Y, Wang Z
Nat Chem. 2024; 16(6):988-997.
PMID: 38443494
DOI: 10.1038/s41557-024-01468-2.
Systematic Assessment of the Catalytic Reactivity of Frustrated Lewis Pairs in C-H Bond Activation.
Guo Y, Lian X, Zhang H, Zhang X, Chen J, Chen C
Molecules. 2024; 29(1).
PMID: 38202607
PMC: 10780200.
DOI: 10.3390/molecules29010024.
Borylation directed borylation of -alkyl anilines using iodine activated pyrazaboles.
Millet C, Noone E, Schellbach A, Pahl J, Losiewicz J, Nichol G
Chem Sci. 2023; 14(43):12041-12048.
PMID: 37969579
PMC: 10631245.
DOI: 10.1039/d3sc04269c.
Reversible Oxidative Addition of Nonactivated C-H Bonds to Structurally Constrained Phosphenium Ions.
Roth D, Radosevich A, Greb L
J Am Chem Soc. 2023; 145(44):24184-24190.
PMID: 37877607
PMC: 10842376.
DOI: 10.1021/jacs.3c08456.
Metal-free C-H Borylation and Hydroboration of Indoles.
Nad P, Mukherjee A
ACS Omega. 2023; 8(41):37623-37640.
PMID: 37867714
PMC: 10586279.
DOI: 10.1021/acsomega.3c05071.
Reversible C-H bond silylation with a neutral silicon Lewis acid.
Thorwart T, Greb L
Chem Sci. 2023; 14(40):11237-11242.
PMID: 37860638
PMC: 10583699.
DOI: 10.1039/d3sc03488g.
Atroposelective Ir-Catalyzed C-H Borylation of Phthalazine Heterobiaryls.
Stehrer P, Spannenberg A, Hapke M
J Org Chem. 2023; 88(19):14222-14226.
PMID: 37751525
PMC: 10563123.
DOI: 10.1021/acs.joc.3c01534.
Main Group Catalyzed Arene Borylation: Challenges and Opportunities.
Ingleson M
ACS Catal. 2023; 13(11):7691-7697.
PMID: 37288098
PMC: 10242676.
DOI: 10.1021/acscatal.3c01668.
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using -Br Sulfoximines as Both Brominating and Sulfoximinating Reagents.
Chen X, Tang Y, Xiang X, Tang Y, Huang M, Zheng S
Molecules. 2023; 28(8).
PMID: 37110617
PMC: 10146707.
DOI: 10.3390/molecules28083380.
Probing the Impact of Solvent on the Strength of Lewis Acids via Fluorescent Lewis Adducts.
Laturski A, Gaffen J, Demay-Drouhard P, Caputo C, Baumgartner T
Precis Chem. 2023; 1(1):49-56.
PMID: 37025975
PMC: 10069026.
DOI: 10.1021/prechem.2c00009.
Group 13 exchange and transborylation in catalysis.
Willcox D, Thomas S
Beilstein J Org Chem. 2023; 19:325-348.
PMID: 36998308
PMC: 10043741.
DOI: 10.3762/bjoc.19.28.
Understanding and Expanding Zinc Cation/Amine Frustrated Lewis Pair Catalyzed C-H Borylation.
Grundy M, Sotorrios L, Kumar Bisai M, Yuan K, Macgregor S, Ingleson M
ACS Catal. 2023; 13(4):2286-2294.
PMID: 36846822
PMC: 9942201.
DOI: 10.1021/acscatal.2c05995.
Metal-Free Intermolecular C-H Borylation of N-Heterocycles at B-B Multiple Bonds.
Bruckner T, Ritschel B, Jimenez-Halla J, Fantuzzi F, Duwe D, Markl C
Angew Chem Int Ed Engl. 2022; 62(5):e202213284.
PMID: 36440659
PMC: 10107673.
DOI: 10.1002/anie.202213284.