Erhong Hao

No. 1 East Beijing Road
Wuhu, 241000, China

Last Updated: 09/26/2026

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Found 113 publications

Tandem Oxidative Nucleophilic Hydrogen Substitution/B-O Cyclization Enables Chiral Near-Infrared N,O,B-Chelated BODIPYs.

Tandem Oxidative Nucleophilic Hydrogen Substitution/B-O Cyclization Enables Chiral Near-Infrared N,O,B-Chelated BODIPYs.

Journal: Organic letters
Published: July 27, 2026

Suppressing reverse intersystem crossing via ring-fusion: turning fluorophores into efficient photosensitizers.

Suppressing reverse intersystem crossing via ring-fusion: turning fluorophores into efficient photosensitizers.

Journal: Chemical communications (Cambridge, England)
Published: July 14, 2026

Unsymmetric 2,3- and 3,6-Disubstituted BODIPYs: Regioselective Synthesis, Reactivity, and Photophysical Properties.

Unsymmetric 2,3- and 3,6-Disubstituted BODIPYs: Regioselective Synthesis, Reactivity, and Photophysical Properties.

Journal: Organic letters
Published: June 12, 2026

Naphthalimide-fused BODIPYs via one-pot quadruple C-H activation: ultra-low LUMO n-type semiconductors with efficient near-infrared emission.

Naphthalimide-fused BODIPYs via one-pot quadruple C-H activation: ultra-low LUMO n-type semiconductors with efficient near-infrared emission.

Journal: Chemical science
Published: June 11, 2026

Bisbenzoselenophene[b]-Fused AzaBODIPYs as Strong Near-Infrared-Absorbing Photosensitizers for Effective Photodynamic Tumor Therapy.

Bisbenzoselenophene[b]-Fused AzaBODIPYs as Strong Near-Infrared-Absorbing Photosensitizers for Effective Photodynamic Tumor Therapy.

Journal: Journal of medicinal chemistry
Published: June 02, 2026

A spirocyclic BODIPY photosensitizer with pH-triggered triplet-state activation for tumor-selective photodynamic therapy.

A spirocyclic BODIPY photosensitizer with pH-triggered triplet-state activation for tumor-selective photodynamic therapy.

Journal: Chemical communications (Cambridge, England)
Published: May 28, 2026

Correction to "Tuning Molecular Rigidity with Seven-Membered Ring Fusion: A Strategy toward Bright Near-Infrared azaBODIPY Fluorophores".

Correction to "Tuning Molecular Rigidity with Seven-Membered Ring Fusion: A Strategy toward Bright Near-Infrared azaBODIPY Fluorophores".

Journal: Organic letters
Published: May 27, 2026

Tuning Molecular Rigidity with Seven-Membered Ring Fusion: A Strategy toward Bright Near-Infrared azaBODIPY Fluorophores.

Tuning Molecular Rigidity with Seven-Membered Ring Fusion: A Strategy toward Bright Near-Infrared azaBODIPY Fluorophores.

Journal: Organic letters
Published: May 08, 2026

Chiral bowl-shaped thiazole-embedded B(III)-azatriphyrins(2.1.1): a nonaromatic platform via triple core-modification.

Chiral bowl-shaped thiazole-embedded B(III)-azatriphyrins(2.1.1): a nonaromatic platform via triple core-modification.

Journal: Chemical communications (Cambridge, England)
Published: March 19, 2026

Modular Access to Boron Tripyrrolic Complexes from a Sequential Buchwald-Hartwig Amination/Boron Complexation Reaction.

Modular Access to Boron Tripyrrolic Complexes from a Sequential Buchwald-Hartwig Amination/Boron Complexation Reaction.

Journal: Organic letters
Published: February 14, 2026

A Palladium(II)-Catalyzed Dehydrogenative Strategy to NIR-Emissive BODIPY Dimers and Trimers with Reactive Oxygen Species Generation Characteristics.

A Palladium(II)-Catalyzed Dehydrogenative Strategy to NIR-Emissive BODIPY Dimers and Trimers with Reactive Oxygen Species Generation Characteristics.

Journal: Organic letters
Published: January 28, 2026

Construction of Chiral 1,2-Azaborines via Rhodium-Catalyzed Enantioselective Carbene N-H Bond Insertion.

Construction of Chiral 1,2-Azaborines via Rhodium-Catalyzed Enantioselective Carbene N-H Bond Insertion.

Journal: Organic letters
Published: December 23, 2025
Showing 1-12 of 113

Last Updated: 09/26/2026