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Fast Enantio‐ and Chemoselective Arylation of Ketones with Organoboronic Esters Enabled by Nickel/N‐Heterocyclic Carbene Catalysis

Angewandte Chemie International Edition, 2021-03, Vol.60 (10), p.5262-5267

International ed. in English, 2021

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Copper‐Catalyzed Enantioselective Markovnikov Protoboration of α‐Olefins Enabled by a Buttressed N‐Heterocyclic Carbene Ligand

Angewandte Chemie International Edition, 2018-01, Vol.57 (5), p.1376-1380

International ed. in English, 2018

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Dynamic kinetic asymmetric arylation and alkenylation of ketones

Science (American Association for the Advancement of Science), 2023-02, Vol.379 (6633), p.662-670

2023

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Diffusion Tensor Imaging With Tract-Based Spatial Statistics Reveals White Matter Abnormalities in Patients With Vascular Cognitive Impairment

Frontiers in neuroanatomy, 2018-06, Vol.12, p.53-53

2018

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Fast Enantio‐ and Chemoselective Arylation of Ketones with Organoboronic Esters Enabled by Nickel/N‐Heterocyclic Carbene Catalysis

Angewandte Chemie, 2021-03, Vol.133 (10), p.5322-5327

2021

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Copper‐Catalyzed Enantioselective Markovnikov Protoboration of α‐Olefins Enabled by a Buttressed N‐Heterocyclic Carbene Ligand

Angewandte Chemie, 2018-01, Vol.130 (5), p.1390-1394

2018

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Dynamic kinetic asymmetric allylation, propargylation and crotylation of ketones using copper catalysis

Nature Synthesis, 2024-09, Vol.3 (9), p.1091-1103

2024

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Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia

PloS one, 2024-10, Vol.19 (10), p.e0310547

2024

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Short-term safety and efficacy of the biodegradable iron stent in mini-swine coronary arteries

Chinese medical journal, 2013, Vol.126 (24), p.4752-4757

2013

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Distribution and Migration of Heavy Metals in Undisturbed Forest Soils： A High Resolution Sampling Method

Pedosphere, 2008-06, Vol.18 (3), p.386-393

2008

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Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

Scientific reports, 2024-04, Vol.14 (1), p.7638-14, Article 7638

2024

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Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

BioMed research international, 2021-05, Vol.2021, p.1-12

2021

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Development a novel nomogram model for predicting significant hepatic histological changes in chronic hepatitis B virus carriers

Journal of medical virology, 2023-07, Vol.95 (7), p.e28943-n/a

2023

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Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome

Journal of medical genetics, 2023-12, Vol.60 (12), p.1210-1214

2023

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A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

The journal of gene medicine, 2022-02, Vol.24 (2), p.e3398-n/a

2022

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Ultrasomics differentiation of malignant and benign focal liver lesions based on contrast-enhanced ultrasound

BMC medical imaging, 2024-09, Vol.24 (1), p.242-12, Article 242

2024

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Multi-Angle method to retrieve infrared spectral properties of a high-transparency material at high temperatures

Solar energy materials and solar cells, 2018-08, Vol.183, p.173-180

2018

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Multi-layer-combination method to retrieve high-temperature spectral properties of C-plane sapphire

International journal of heat and mass transfer, 2018-06, Vol.121, p.1011-1020

2018

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Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier

Digestive diseases and sciences, 2024-06, Vol.69 (6), p.2109-2122

2024

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Exposing Cu(100) Surface via Ion-Implantation-Induced Oxidization and Etching for Promoting Hydrogen Evolution Reaction

Langmuir, 2022-03, Vol.38 (9), p.2993-2999

2022

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Function of PHEX mutations p.Glu145 and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

Cell death & disease, 2022-06, Vol.13 (6), p.518-518, Article 518

2022

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Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family

Neurological sciences, 2022-04, Vol.43 (4), p.2555-2563

2022

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Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

Pediatric rheumatology online journal, 2023-10, Vol.21 (1), p.130-130, Article 130

2023

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Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report

Annals of hematology, 2024-05, Vol.103 (5), p.1765-1774

2024

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A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification

BMC pulmonary medicine, 2024-07, Vol.24 (1), p.343-13, Article 343

2024

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Fast Enantio‐ and Chemoselective Arylation of Ketones with Organoboronic Esters Enabled by Nickel/N‐Heterocyclic Carbene Catalysis

Copper‐Catalyzed Enantioselective Markovnikov Protoboration of α‐Olefins Enabled by a Buttressed N‐Heterocyclic Carbene Ligand

Dynamic kinetic asymmetric arylation and alkenylation of ketones

Diffusion Tensor Imaging With Tract-Based Spatial Statistics Reveals White Matter Abnormalities in Patients With Vascular Cognitive Impairment

Fast Enantio‐ and Chemoselective Arylation of Ketones with Organoboronic Esters Enabled by Nickel/N‐Heterocyclic Carbene Catalysis

Copper‐Catalyzed Enantioselective Markovnikov Protoboration of α‐Olefins Enabled by a Buttressed N‐Heterocyclic Carbene Ligand

Dynamic kinetic asymmetric allylation, propargylation and crotylation of ketones using copper catalysis

Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia

Short-term safety and efficacy of the biodegradable iron stent in mini-swine coronary arteries

Distribution and Migration of Heavy Metals in Undisturbed Forest Soils： A High Resolution Sampling Method

Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

Development a novel nomogram model for predicting significant hepatic histological changes in chronic hepatitis B virus carriers

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

Ultrasomics differentiation of malignant and benign focal liver lesions based on contrast-enhanced ultrasound

Multi-Angle method to retrieve infrared spectral properties of a high-transparency material at high temperatures

Multi-layer-combination method to retrieve high-temperature spectral properties of C-plane sapphire

Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier

Exposing Cu(100) Surface via Ion-Implantation-Induced Oxidization and Etching for Promoting Hydrogen Evolution Reaction

Function of PHEX mutations p.Glu145 and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family

Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report

A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification

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