L. Yao

发表

Advances and perspectives of proteolysis targeting chimeras (PROTACs) in drug discovery.

Jiayue Xi, Ruyue Zhang, Muqiong Li, 2022, Bioorganic chemistry.

Antisense locked nucleic acids targeting agrA inhibit quorum sensing and pathogenesis of community‐associated methicillin‐resistant Staphylococcus aureus

X. Luo, X. Xue, Z. Hou, 2017, Journal of applied microbiology.

A practical strategy to access chiral α-aryloxy carboxylic acids through ion-pairing directed asymmetric hydrogenation

Hai-xia Ma, Huifang Nie, Dongxu Zhang, 2020 .

Highly enantioselective hydrogenation of α-oxy functionalized α,β-unsaturated acids catalyzed by a ChenPhos-Rh complex in CF3CH2OH.

Xumu Zhang, J. Wen, Shengyong Zhang, 2016, Chemical communications.

Promotion of Henry reactions using Cu(OTf)2 and a sterically hindered Schiff base: access to enantioenriched β-hydroxynitroalkanes

Wei He, Yu Wei, Shengyong Zhang, 2012 .

Novel Schiff base ligands derived from Cinchona alkaloids for Cu(II)-catalyzed asymmetric Henry reaction

Wei He, Yu Wei, Shengyong Zhang, 2011 .

Concise asymmetric synthesis of two natural oxacyclododecindione-type macrolactones from industrial waste

Huifang Nie, Weiping Chen, L. Yao, 2020, RSC advances.

Chiral Ferrocenyl N,N Ligands with Intramolecular Hydrogen Bonds for Highly Enantioselective Allylic Alkylations

Zhenhua Li, Huifang Nie, Dongxu Zhang, 2018 .

Josiphos-Type Binaphane Ligands for Iridium-Catalyzed Enantioselective Hydrogenation of 1-Aryl-Substituted Dihydroisoquinolines.

Huifang Nie, Shengyong Zhang, L. Yao, 2019, Organic letters.

Stereoselective synthesis of α-diazo oxime ethers and their application in the synthesis of highly substituted pyrroles through a [3+2] cycloaddition.

Cheol‐Min Park, L. Yao, E. Lourdusamy, 2010, Angewandte Chemie.

Highly efficient synthesis of chiral aromatic ketones via Rh-catalyzed asymmetric hydrogenation of β,β-disubstituted enones.

Xumu Zhang, Jun Jiang, Tao Zhang, 2017, Chemical communications.

Highly Regio- and Enantioselective Hydrogenation of Conjugated α-Substituted Dienoic Acids.

Y. Lan, Song Liu, Weiping Chen, 2020, Organic letters.

Stereoselective Synthesis of α‐Diazo Oxime Ethers and Their Application in the Synthesis of Highly Substituted Pyrroles Through a [3 + 2] Cycloaddition.

Cheol‐Min Park, L. Yao, E. Lourdusamy, 2011 .

Highly Chemo- and Enantioselective Hydrogenation of 2-Substituted-4-oxo-2-alkenoic Acids.

Xumu Zhang, J. Wen, Huifang Nie, 2020, Organic letters.

Iridium-catalyzed enantioselective reductive amination of aromatic ketones

W. Zhao, Huifang Nie, Dongxu Zhang, 2020 .

Iridium-Catalyzed Asymmetric Hydrogenation of Sterically Hindered Cyclic Imines for Enantioselective Synthesis of Tetrahydroisoquinolines.

Jing Yang, Shengyong Zhang, Huifang Nie, 2020, Organic letters.

Discovery of Novel Non-Oxime Reactivators Showing In Vivo Antidotal Efficiency for Sarin Poisoned Mice

Xinlei Zhang, Huifang Nie, Qin Ouyang, 2022, Molecules.

Molecular modeling-guided optimization of acetylcholinesterase reactivators: A proof for reactivation of covalently inhibited targets

Jun Yang, Huifang Nie, L. Yao, 2021, European Journal of Medicinal Chemistry.

Design, synthesis and evaluation of new classes of nonquaternary reactivators for acetylcholinesterase inhibited by organophosphates.

Shengzheng Wang, Huifang Nie, Jun Yang, 2018, Bioorganic chemistry.

Conjugates of salicylaldoximes and peripheral site ligands: Novel efficient nonquaternary reactivators for nerve agent-inhibited acetylcholinesterase.

Shengzheng Wang, Huifang Nie, Xueying Liu, 2017, Bioorganic & medicinal chemistry.

3-aminoacyl-tetrahydrothiazole-2-thione as an active amide for peptide synthesis (I)

Hsing Chi-yi, L. Yao, Li Chung-hsi, 1981 .

Very Simple and Highly Modular Synthesis of Ferrocene-Based Chiral Phosphines with a Wide Variety of Substituents at the Phosphorus Atom(s)

Huifang Nie, Shengyong Zhang, Weiping Chen, 2014 .

2-Oxy-3-Phenylacrylic Acid Derivatives as Potent Mcl-1 Inhibitors for Treatment of Cancer

Jiayue Xi, Huifang Nie, Dongxu Zhang, 2022, SSRN Electronic Journal.

Conjugates of salicylaldoximes and peripheral site ligands: Novel efficient nonquaternary reactivators for nerve agent-inhibited acetylcholinesterase.

Shengzheng Wang, Xueying Liu, Song Li, 2017, Bioorganic & medicinal chemistry.