about
Stereoselective alkoxycarbonylation of unactivated C(sp3)-H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis.Stereoselective Synthesis of Chiral β-Fluoro α-Amino Acids via Pd(II)-Catalyzed Fluorination of Unactivated Methylene C(sp(3))-H Bonds: Scope and Mechanistic Studies.Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study.Synthesis of chiral α-hydroxy acids via palladium-catalyzed C(sp(3))-H alkylation of lactic acid.Redox-Activated Light-Up Nanomicelle for Precise Imaging-Guided Cancer Therapy and Real-Time Pharmacokinetic Monitoring.Copper-Catalyzed Enantioselective Markovnikov Protoboration of α-Olefins Enabled by a Buttressed N-Heterocyclic Carbene Ligand.Mechanisms and Origins of Chemo- and Regioselectivities of Ru(II)-Catalyzed Decarboxylative C-H Alkenylation of Aryl Carboxylic Acids with Alkynes: A Computational Study.Stereoretentive C(sp3)–S Cross-CouplingAlternate Heme Ligation Steers Activity and Selectivity in Engineered Cytochrome P450-Catalyzed Carbene-Transfer ReactionsStepwise versus Concerted Reductive Elimination Mechanisms in the Carbon–Iodide Bond Formation of (DPEphos)RhMeI2 ComplexN-Heterocyclic Carbene–Cu-Catalyzed Enantioselective Allenyl Conjugate AdditionPalladium-Catalyzed Selective Five-Fold Cascade Arylation of the 12-Vertex Monocarborane Anion by B–H ActivationRhodium-Catalyzed Asymmetric Addition of Organoboronic Acids to Aldimines Using Chiral Spiro Monophosphite-Olefin Ligands: Method Development and Mechanistic StudiesMechanism and Origins of Chemo- and Regioselectivities of Pd-Catalyzed Intermolecular σ-Bond Exchange between Benzocyclobutenones and Silacyclobutanes: A Computational StudyN-heterocyclic Carbene–Cu-Catalyzed Enantioselective Conjugate Additions with Alkenylboronic Esters as NucleophilesPalladium-catalyzed C(sp3)–H arylation of lactic acid: efficient synthesis of chiral β-aryl-α-hydroxy acidsPractical Synthesis of anti -β-Hydroxy-α-Amino Acids by PdII -Catalyzed Sequential C(sp3 )H FunctionalizationA general and practical palladium-catalyzed monoarylation of β-methyl C(sp3)–H of alaninePalladium(0)-catalyzed cyclopropanation of benzyl bromides via C(sp3)–H bond activationPd(ii)-catalyzed alkoxylation of unactivated C(sp3)–H and C(sp2)–H bonds using a removable directing group: efficient synthesis of alkyl ethersPd(ii)-catalyzed alkylation of unactivated C(sp3)–H bonds: efficient synthesis of optically active unnatural α-amino acidsEngineered Cytochrome -Catalyzed Lactone-Carbene B-H InsertionComputation-Guided Development of the "Click" ortho-Quinone Methide Cycloaddition with Improved KineticsRhodium(III)-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Dienes: An Experimental and DFT StudyNucleophile-Dependent Z/ E- and Regioselectivity in the Palladium-Catalyzed Asymmetric Allylic C-H Alkylation of 1,4-DienesA Unified Explanation for Chemoselectivity and Stereospecificity of Ni-Catalyzed Kumada and Cross-Electrophile Coupling Reactions of Benzylic Ethers: A Combined Computational and Experimental StudyC-H Acidity and Arene Nucleophilicity as Orthogonal Control of Chemoselectivity in Dual C-H Bond ActivationComputational studies on Ni-catalyzed amide C-N bond activation
P50
Q37315229-A0F7800B-8E25-4D19-B76B-84C602B3C04CQ40843253-6B445445-81E8-49D7-96E1-7235E5925470Q46705158-2669C857-0BE6-4327-8ED0-D4D5BE79C239Q46933137-9C45EAFE-178F-4F82-B55B-FB550E5BA3DCQ48117093-E3CD9BDD-8822-4388-BC4A-E4BE65ED7FD0Q48135982-08B42151-ABF8-4F91-A75D-3DF5793D40D7Q48151445-A27E117E-F03C-4C6E-BD76-8A2F1DF78ACAQ59780996-BBA4BCF7-90AA-41B7-804B-1FB95C106529Q59780997-C34DF338-D241-4B88-B99A-BFCB0B5EC820Q59780998-60A20678-12EF-4883-B466-91D6A227FBF6Q59780999-11C0EBDA-D500-468E-B7DC-B8285788C270Q59781000-7774CBA3-3928-41E5-BF2E-FA05ED822C8DQ59781001-3B324709-CF24-421A-B164-9AE06F485EEAQ59781002-543C5E07-4248-48F0-B2E5-AA92A798A988Q59781003-EC565FC5-6065-45B6-A30D-2C63009505CDQ59781004-31AA3790-64B6-445F-BA23-CC952C0BFBC0Q59781005-886AE6EB-97C5-4F60-B08A-8B93D32E0C5DQ59781006-C726D474-D28E-4586-81BF-5C2BC5185DC1Q59781008-2F58B4F5-149B-45FA-9FB5-354E571EC0BBQ59781009-FAECC97B-5A8E-4BBD-8511-AB4FBBE0E04BQ59781010-94861F44-8307-43CB-B94A-9E6874481E03Q64282131-0188A25D-E3FD-45A1-B906-90C297E034D7Q91628751-4EC6B679-D467-4E8F-BA52-9A243FC5E35EQ92179187-00D747D3-4CCA-48B4-92BB-CA6F1870A134Q92306948-E4439C28-A9BD-4A58-ABEC-8095C044433AQ92335892-FCA56A69-5A46-46C1-80E2-B0798CAD96ADQ92502043-38C92D2E-E104-40A8-911A-68D8F76FC3A2Q95572767-5098D5FC-A1D3-418E-9442-BC76DED5FF69
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Shuo-Qing Zhang
@ast
Shuo-Qing Zhang
@en
Shuo-Qing Zhang
@es
Shuo-Qing Zhang
@nl
Shuo-Qing Zhang
@sl
type
label
Shuo-Qing Zhang
@ast
Shuo-Qing Zhang
@en
Shuo-Qing Zhang
@es
Shuo-Qing Zhang
@nl
Shuo-Qing Zhang
@sl
altLabel
Shuo-qing Zhang
@en
Shuoqing Zhang
@en
prefLabel
Shuo-Qing Zhang
@ast
Shuo-Qing Zhang
@en
Shuo-Qing Zhang
@es
Shuo-Qing Zhang
@nl
Shuo-Qing Zhang
@sl
P1053
N-7902-2017
P106
P31
P3829
P496
0000-0002-7617-3042