Hongyin Gao
0000-0003-4049-6832
Shandong University
16 papers found
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Desulfurdioxidative N‐N Coupling of N‐Arylhydroxylamines and N‐Sulfinylanilines: Reaction Development and Mechanism
Antimicrobial activity of a natural compound and analogs against multi-drug-resistant Gram-positive pathogens
Regioselective umpolung para-C–H functionalization of arylhydroxylamines
Synthesis of ortho-Phosphated (Hetero)Arylamines through Cascade Atherton–Todd Reaction/[3,3]-Rearrangement from Arylhydroxylamines and Dialkyl Phosphites
Transition-Metal-Free Cascade Approach for the Synthesis of Functionalized Biaryls by SNAr of Arylhydroxylamines with Arylsulfonium Salts
[2,3]-Sigmatropic Rearrangement of Arylhydroxylamines: Rapid Access to ortho-Sulfonylated Anilines
Expeditious and Efficient ortho ‐Selective Trifluoromethane‐sulfonylation of Arylhydroxylamines
Rapid Access to Fluorinated Anilides via DAST-Mediated Deoxyfluorination of Arylhydroxylamines
Practical bromination of arylhydroxylamines with SOBr2 towards ortho-bromo-anilides
Cascade Chan‐Lam C‐O Coupling/[3,3]‐Rearrangement of Arylhydroxylamines with Arylboronic Acids Toward NOBIN Analogues
Synthesis of non-C2symmetrical NOBIN-type biaryls through a cascadeN-arylation and [3,3]-sigmatropic rearrangement fromO-arylhydroxylamines and diaryliodonium salts
Transition-metal-free aerobic C–O bond formation via C–N bond cleavage
Tandem approach to NOBIN analogues from arylhydroxylamines and diaryliodonium saltsvia[3,3]-sigmatropic rearrangement
Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines
Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles
Transition metal-free direct dehydrogenative arylation of activated C(sp3)–H bonds: synthetic ambit and DFT reactivity predictions
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