Publications
82.) Zhang, G.-W.; Ge, H.-B.* Asymmetric C–C bond functionalization. (to be submitted)
81.) Zhang, G.-W.; Ge, H.-B.* Nickel-catalyzed alkyne C–C bond functionalization. (to be submitted)
80.) Ge, R.; Herington, F.; Mangawang, A.; Maiti, D.* Ge, H.-B.* Pd-Catalyzed Cascade Reactions via Directed Functionalization of Unactivated C-H Bonds. (submitted)
79.) Liu, C.; Ge, R.; Chen, J.; Guo, H.-M.; Bartholomore, T.; Maiti, D.* Ge, H.-B.* Facile Construction of Distal and Diversified Tertiary and Quaternary Stereocenters. (submitted)
78.) Zhang, G.-W.; Ge, H.-B.* Palladium-catalyzed selective C–F bond functionalization. (submitted)
77.) Pradhan, S.; Biswas, J. P.; Elsaid, M.; Ge, H.-B.* Maiti, D.* Selectivity Switch in Distal C-H Arylation of 1-Naphthamides. (under revision)
76.) Yang, K.; Yuan, D.; Herington, F.; Ge, H.-B.* Removable Template-Assisted Transition Metal-Catalyzed Distal C–H Functionalization. In 'Directed C-H Bond Functionalization: Concepts and Applications'. (accepted)
75.) Ge, R.; Yang, K.; Ge, H.-B.* Nickel-Catalyzed C–H Bond Functionalization for Nitrogen-Containing Heterocycles. In 'Functionalisation of Heterocycles through Transition Metal Catalyzed C-H Activation. (accepted)
74.) Li, Q.; Yuan, D.; Liu, C.; Herington, F.; Yang, K.; Ge, H.-B.* An Environmentally Friendly Method for Oxidation of Sulfides. Molecules 2024, DOI:10.3390/molecules29163899
73.) Dutta, B.; Mahajan, M.; Ghosh, A.; Dajek, M.; Kowalczyk, R.;* Mondal, B.;* Ge, H.-B.;* Zhang, X.-L.;* Maiti, D.* Hydrogen bonding template enables meta-C-H alkenylation of Nitroarenes. Nat. Commun. 2024, DOI: 10.1038/s41467-024-51764-1
72.) Zhang, J.X.; Sun, T.; Wang, K.-M.; Hu, R.-K.; Zhou, C.-L.; Ge, H.-B.* Li, B.-J.* Rh(III)-Catalyzed Build-Up Fused Heterocyclic Cations: Facile Access to White-Light-Emitting Materials. Chem. Sci. 2024, DOI: 10.1039/D4SC02188F
71.) Pal, T.; Ghosh, P.; Islam, M.; Guin, S.; Maji, S.; Dutta, S.; Das, J.; Ge, H.-B.;* Maiti, D.* Tandem dehydrogenation-olefination -decarboxylation of cycloalkyl carboxylic acids via multifold C-H activation. Nat. Commun. 2024, DOI: 10.1038/s41467-024-49359-x
70.) Ge, R.; Xu, Z.-T.; Yang, K.;* Ge, H.-B.* Transition Metal-Catalyzed C(sp3)–H Bond Fluorination Reactions. Chem. Catal. 2024, DOI: 10.1016/j.checat.2024.101009
69.) Xu, Z.; Li, Z.; Liu, C.; Yang, K.; Ge, H. Palladium-Catalyzed β-C(sp3)–H Bond Arylation of Tertiary Aldehydes Facilitated by 2-Pyridone Ligands. Molecules 2024, 29, 259. DOI: 10.3390/molecules29010259
67.) Bhattacharya, T.; Ghosh, S.; Dutta, S.; Guin, S.; Ge, H.-B.;* Sunoj, R. B.;* Maiti, D.* Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C-H Allylation. Angew. Chem. Int. Ed. 2023, DOI: 10.1002/anie.202310112
66.) Das, J.; Ali, W.; Ghosh, A.; Pal, T.; Mandal, A.; Teja, C.; Dutta, S.; Pothikumar, R.; Ge, H.-B.;* Zhang, X.-L.;* Maiti, D.* Access to Unsaturated Bicyclic Lactones by Overriding Conventional C(sp3)‒H Site Selectivity. Nat. Chem, 2023, doi: 0.1038/s41557-023-01295-x.
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50.) Li, B.; Lawrence, B.; Li, G.; Ge, H. Ligand-Controlled Direct gamma-C-H Arylation of Aldehydes. Angew. Chem. 2020, 59, 3078-3082.
49.) Yang, K.; Niu, B.; Ma, Z.; Wang, H.; Lawrence, B.; Ge, H. Silver-Promoted Site-Selective Intramolecular Cyclization of 2-Methylthiobenzamide Through alpha-C(sp(3))-H Functionalization. J. Org. Chem. 2019, 84, 14045-14052.
42.) Mei, Y.; Ye, Q.; Yang, B.; Xiao, L.; Ge, H. Novel synthesis method of ataluren. From Faming Zhuanli Shenqing (2017), CN 106279057 A 20170104.
41.) Ye, Q.; Ge, H.; Mei, Y.; Xiao, L. Process for synthesizing fingolimod. From Faming Zhuanli Shenqing (2017), CN 106397224 A 20170215.​
40.) Liu, Y.; Ge, H. Site-selective C-H arylation of primary aliphatic amines enabled by a catalytic transient directing group. Nat. Chem. 2017, 9, 26-32.
18.) Wu, X.-S.; Zhao, Y.; Ge, H.-B. Nickel-Catalyzed Site-Selective Alkylation of Unactivated C(sp3 )–H Bonds, Synform, 2014, DOI: 10.1055/s-0033-1341123
4.) Peng, Y.-L.; Li, Q.; Liu, X.-G.; Yang, X.-L.; Ge, H.-B.; Chen, X.-F. “A New Method for The Preparation of Methyl tri-O-Benzoyl-4-deoxy-4-fluoro-a-D-glucopyranoside. CN 101245086, 2008.