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Fangfang Shen

University of Hong Kong

H指数:14

被引数:1,125

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Engineering Cell-Specific Protein Delivery Vehicles for Erythroid Lineage Cells

ACS BIO & MED CHEM AU

IF4.3

2025-02-270

OAAI

Opportunities and challenges of protein-based targeted protein degradation

CHEMICAL SCIENCE

IF7.4

2023-01-0115

OAAI

A Cell-Permeant Nanobody-Based Degrader That Induces Fetal Hemoglobin

一种可渗透细胞的基于纳米抗体的降解剂，可诱导胎儿血红蛋白

ACS CENTRAL SCIENCE

IF10.4

2022-12-1419

OAAI

CircRNA circ-NNT mediates myocardial ischemia/reperfusion injury through activating pyroptosis by sponging miR-33a-5p and regulating USP46 expression

CELL DEATH DISCOVERY

IF7

2021-11-2933

OAAI

Mediating K+/H+ Transport on Organelle Membranes to Selectively Eradicate Cancer Stem Cells with a Small Molecule

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2020-05-2238

PREAI

A small synthetic molecule functions as a chloride-bicarbonate dual-transporter and induces chloride secretion in cells

CHEMICAL COMMUNICATIONS

IF4.2

2016-01-0120

OAAI

Catalytic Asymmetric 1,2-Addition of α-Isothiocyanato Phosphonates: Synthesis of Chiral β-Hydroxy- or β-Amino-Substituted α-Amino Phosphonic Acid Derivatives

Α-异硫氰酸酯的催化不对称1，2-加成: 手性 β-羟基或 β-氨基取代的 α-氨基膦酸衍生物的合成

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2014-01-1337

PREAI

Catalytic Enantioselective Ring-Opening Reaction of meso-Aziridines with -Isothiocyanato Imides

CHEMISTRY-A EUROPEAN JOURNAL

IF3.7

2013-06-0733

PREAI

Catalytic Asymmetric Michael Addition/Cyclization of Isothiocyanato Oxindoles: Highly Efficient and Versatile Approach for the Synthesis of 3,2'-Pyrrolidinyl Mono- and Bi-spirooxindole Frameworks

CHEMISTRY-A EUROPEAN JOURNAL

IF3.7

2012-12-18143

PREAI

Enantioselective Michael/Cyclization Reaction Sequence: Scaffold-Inspired Synthesis of Spirooxindoles with Multiple Stereocenters

对映选择性Michael/环化反应序列: 具有多个立体中心的螺氧吲哚的支架启发合成

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2011-08-25258

OAAI

A Unique Approach to the Concise Synthesis of Highly Optically Active Spirooxazolines and the Discovery of a More Potent Oxindole-Type Phytoalexin Analogue

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2010-10-12292

PRE

Direct Organocatalytic Asymmetric Aldol Reaction of α-Isothiocyanato Imides to α-Ketoesters under Low Ligand Loading: A Doubly Stereocontrolled Approach to Cyclic Thiocarbamates Bearing Chiral Quaternary Stereocenters

ORGANIC LETTERS

IF5

2010-03-0568

PREAI