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Biphasic Enantioselective Fluorescent Recognition of Amino Acids by a Fluorophilic Probe

Chemistry : a European journal, 2019-06, Vol.25 (33), p.7866-7873

2019

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E3 ligase ligand optimization of Clinical PROTACs

Frontiers in chemistry, 2023-01, Vol.11, p.1098331-1098331

2023

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Modular Assembly of Six‐Membered Carbocyclic Spirooxindoles via Peterson Olefination/Michael Addition/C(sp3) Arylation Cascade

Chinese journal of chemistry, 2024-11, Vol.42 (21), p.2614-2620

2024

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Free Amino Acid Recognition: A Bisbinaphthyl-Based Fluorescent Probe with High Enantioselectivity

Journal of the American Chemical Society, 2019-01, Vol.141 (1), p.175-181

2019

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Recent Advances in the Chemical Synthesis of β-Nicotinamide Mononucleotide

Current organic chemistry, 2022-01, Vol.26 (24), p.2151-2159

2022

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Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

Bioorganic & medicinal chemistry, 2022-02, Vol.55, p.116597-116597, Article 116597

2022

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Synthesis of Deoxy Pyranosides Via Fe(III) Catalyzed Regioselective Thiocarbonylation of Partially Protected Carbohydrates

European journal of organic chemistry, 2024-07

2024

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Iridium-Catalyzed Intramolecular Asymmetric Allylation of Vinyl Benzoxazinones for the Synthesis of Chiral 4H‑3,1-Benzoxazines via Kinetic Resolution

Organic letters, 2023-02, Vol.25 (7), p.1172-1177

2023

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Quinolines and isoquinolines as HIV-1 inhibitors: Chemical structures, action targets, and biological activities

Bioorganic chemistry, 2023-07, Vol.136, p.106549-106549, Article 106549

2023

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Advances in rationally designed dual inhibitors of HIV-1 reverse transcriptase and integrase

Bioorganic & medicinal chemistry, 2016-11, Vol.24 (21), p.5007-5016

2016

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Preparation of (S)-3,3ʹ-Bis(1-pyrrolidinylmethyl)-5,5ʹ,6,6ʹ, 7,7ʹ,8,8ʹ-octahydro-1,1'-bi-2-naphthol

Organic syntheses, 2023, Vol.100, p.394-403

Hong, Yu

2023

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Preparation of (S)-5,5ʹ,6,6ʹ,7,7ʹ,8,8ʹ-Octahydro-1,1'-bi-2-naphthol [(S)-H8BINOL]

Organic syntheses, 2023, Vol.100, p.404-417

Chen, Jiong

2023

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Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-07, Vol.19 (14), p.4220-4226

2011

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Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review

Bioorganic chemistry, 2024-06, Vol.147, p.107380-107380, Article 107380

2024

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Chiral amino acid recognition in water: A BINOL-based fluorescent probe

Chinese chemical letters, 2023-12, Vol.34 (12), p.108345, Article 108345

2023

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An Efficient Method for Removal of Residual Palladium from Organic Solution of Faropenem Sodium in the Pd(II)-Catalyzed Cleavage of Allyl Faropenem

Organic process research & development, 2010-07, Vol.14 (4), p.939-941

2010

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Structural modifications of diarylpyrimidines (DAPYs) as HIV-1 NNRTIs: Synthesis, anti-HIV activities and SAR

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (8), p.2491-2497

2017

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Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-08, Vol.19 (16), p.4704-4709

2011

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A novel family of diarylpyrimidines (DAPYs) featuring a diatomic linker: Design, synthesis and anti-HIV activities

Bioorganic & medicinal chemistry, 2015-10, Vol.23 (20), p.6587-6593

2015

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Design and synthesis of hybrids of diarylpyrimidines and diketo acids as HIV-1 inhibitors

Bioorganic & medicinal chemistry letters, 2017-04, Vol.27 (8), p.1640-1643

2017

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A Scalable One-Pot Process for the Synthesis of Florfenicol Phosphodiester

Organic process research & development, 2014-04, Vol.18 (4), p.552-554

2014

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Synthesis and structure–activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIs

Bioorganic & medicinal chemistry, 2011-09, Vol.19 (17), p.5117-5124

2011

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Simple and Efficient One-Step Synthesis of a Highly Enantioselective Catalyst 3,3′-Di(pyrrolidinylmethyl)-H8BINOL

Synthetic communications, 2015-07, Vol.45 (13), p.1541-1545

2015

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Design, synthesis and biological evaluation of cycloalkyl arylpyrimidines (CAPYs) as HIV-1 NNRTIs

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (23), p.7093-7099

2011

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Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-08, Vol.19 (15), p.4601-4607

2011

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Biphasic Enantioselective Fluorescent Recognition of Amino Acids by a Fluorophilic Probe

E3 ligase ligand optimization of Clinical PROTACs

Modular Assembly of Six‐Membered Carbocyclic Spirooxindoles via Peterson Olefination/Michael Addition/C(sp3) Arylation Cascade

Free Amino Acid Recognition: A Bisbinaphthyl-Based Fluorescent Probe with High Enantioselectivity

Recent Advances in the Chemical Synthesis of β-Nicotinamide Mononucleotide

Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

Synthesis of Deoxy Pyranosides Via Fe(III) Catalyzed Regioselective Thiocarbonylation of Partially Protected Carbohydrates

Iridium-Catalyzed Intramolecular Asymmetric Allylation of Vinyl Benzoxazinones for the Synthesis of Chiral 4H‑3,1-Benzoxazines via Kinetic Resolution

Quinolines and isoquinolines as HIV-1 inhibitors: Chemical structures, action targets, and biological activities

Advances in rationally designed dual inhibitors of HIV-1 reverse transcriptase and integrase

Preparation of (S)-3,3ʹ-Bis(1-pyrrolidinylmethyl)-5,5ʹ,6,6ʹ, 7,7ʹ,8,8ʹ-octahydro-1,1'-bi-2-naphthol

Preparation of (S)-5,5ʹ,6,6ʹ,7,7ʹ,8,8ʹ-Octahydro-1,1'-bi-2-naphthol [(S)-H8BINOL]

Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors

Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review

Chiral amino acid recognition in water: A BINOL-based fluorescent probe

An Efficient Method for Removal of Residual Palladium from Organic Solution of Faropenem Sodium in the Pd(II)-Catalyzed Cleavage of Allyl Faropenem

Structural modifications of diarylpyrimidines (DAPYs) as HIV-1 NNRTIs: Synthesis, anti-HIV activities and SAR

Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors

A novel family of diarylpyrimidines (DAPYs) featuring a diatomic linker: Design, synthesis and anti-HIV activities

Design and synthesis of hybrids of diarylpyrimidines and diketo acids as HIV-1 inhibitors

A Scalable One-Pot Process for the Synthesis of Florfenicol Phosphodiester

Synthesis and structure–activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIs

Simple and Efficient One-Step Synthesis of a Highly Enantioselective Catalyst 3,3′-Di(pyrrolidinylmethyl)-H8BINOL

Design, synthesis and biological evaluation of cycloalkyl arylpyrimidines (CAPYs) as HIV-1 NNRTIs

Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

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