2026
2026
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
2025
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
2024
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
2023
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
2022
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
2021
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
Pre-NKU
Shen, J.-Y.; Cheng, J.-K.; Wang, Y.; Yuan, Z.*; Wang, F.* Amine/Ammonium Buffering Enables Efficient anti-Markovnikov Hydroamination of Olefins with Alkylamines. Nat. Commun. 2026, 17, 8695.
Fan, F.-X.+; Jia, S.-M.+; Mo, Z.; Wang, F.* Iron-Catalyzed Asymmetric NH2-Amination of Sulfenamides. Angew. Chem. Int. Ed. 2026, 65, e1625296. (+These authors contribute equally to this work)
Highlighted in Synfacts by Prof. Martin Oestreich
Zhong, Y.-F.; Xu, H.; Tang, S.-X.; Jia, Z.-Y.; Yang, P.-P.; Mo, Z.; Dang, Y.*; Wang, F.* N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes. J. Am. Chem. Soc. 2026, 148, 26649–26660.
Huang, G.-W.; Mo, Z.; Wang, F.* Hydroxylamine Hydrochloride as Bifunctional Reagent for Aminochlorination of Alkenes via Iron Catalysis. Angew. Chem. Int. Ed. 2026, 65, e1428961.
Highlighted in Synfacts by Prof. Mark Lautens
