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(WKP)Q43178316
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scopus
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(OCoLC)Q43178316
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Fang Liu
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ast
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nl
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es
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sl
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400
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0 |
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Fang Liu
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researcher (ORCID 0000-0002-0046-8434)
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en
|
670
|
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|
‡a
Author's 1,2,4-Triazines Are Versatile Bioorthogonal Reagents.
|
670
|
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|
‡a
Author's 1,3-Dipolar Cycloaddition Reactions of Low-Valent Rhodium and Iridium Complexes with Arylnitrile N-Oxides
|
670
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‡a
Author's Aziridine nitrogen inversion by dynamic NMR: activation parameters in a fused bicyclic structure
|
670
|
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|
‡a
Author's Bialternacins A-F, Aromatic Polyketide Dimers from an Endophytic Alternaria sp
|
670
|
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|
‡a
Author's Bioorthogonal Cycloadditions: Computational Analysis with the Distortion/Interaction Model and Predictions of Reactivities.
|
670
|
|
|
‡a
Author's Bioorthogonal release of sulfonamides and mutually orthogonal liberation of two drugs
|
670
|
|
|
‡a
Author's Biosynthesis of Strained Piperazine Alkaloids - Uncovering the Concise Pathway of Herquline A.
|
670
|
|
|
‡a
Author's Control and design of mutual orthogonality in bioorthogonal cycloadditions
|
670
|
|
|
‡a
Author's Diazo Esters as Dienophiles in Intramolecular
|
670
|
|
|
‡a
Author's Diazo Esters as Dienophiles in Intramolecular (4 + 2) Cycloadditions: Computational Explorations of Mechanism.
|
670
|
|
|
‡a
Author's Diels-Alder Reactivities of Benzene, Pyridine, and Di-, Tri-, and Tetrazines: The Roles of Geometrical Distortions and Orbital Interactions
|
670
|
|
|
‡a
Author's Diels-Alder reactivities of strained and unstrained cycloalkenes with normal and inverse-electron-demand dienes: activation barriers and distortion/interaction analysis
|
670
|
|
|
‡a
Author's Holy Grails for Computational Organic Chemistry and Biochemistry
|
670
|
|
|
‡a
Author's Isomeric triazines exhibit unique profiles of bioorthogonal reactivity
|
670
|
|
|
‡a
Author's Molecular Basis for the Final Oxidative Rearrangement Steps in Chartreusin Biosynthesis
|
670
|
|
|
‡a
Author's Molecular dynamics of the Diels-Alder reactions of tetrazines with alkenes and N2 extrusions from adducts
|
670
|
|
|
‡a
Author's Origins of halogen effects in bioorthogonal sydnone cycloadditions
|
670
|
|
|
‡a
Author's Reversible photochemically gated transformation of a hemicarcerand to a carcerand
|
670
|
|
|
‡a
Author's The expanding world of biosynthetic pericyclases: cooperation of experiment and theory for discovery
|
670
|
|
|
‡a
Author's Theoretical elucidation of the origins of substituent and strain effects on the rates of Diels-Alder reactions of 1,2,4,5-tetrazines
|
909
|
|
|
‡a
(orcid) 0000000200468434
‡9
1
|
909
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|
|
‡a
(scopus) 57091770800
‡9
1
|
919
|
|
|
‡a
124triazinesareversatilebioorthogonalreagents
‡A
1,2,4-Triazines Are Versatile Bioorthogonal Reagents.
‡9
1
|
919
|
|
|
‡a
13dipolarcycloadditionreactionsoflowvalentrhodiumandiridiumcomplexeswitharylnitrilenoxides
‡A
1,3-Dipolar Cycloaddition Reactions of Low-Valent Rhodium and Iridium Complexes with Arylnitrile N-Oxides
‡9
1
|
919
|
|
|
‡a
aziridinenitrogeninversionbydynamicnmractivationparametersinafusedbicyclicstructure
‡A
Aziridine nitrogen inversion by dynamic NMR: activation parameters in a fused bicyclic structure
‡9
1
|
919
|
|
|
‡a
bialternacinsafaromaticpolyketidedimersfromanendophyticalternariasp
‡A
Bialternacins A-F, Aromatic Polyketide Dimers from an Endophytic Alternaria sp
‡9
1
|
919
|
|
|
‡a
bioorthogonalcycloadditionscomputationalanalysiswiththedistortioninteractionmodelandpredictionsofreactivities
‡A
Bioorthogonal Cycloadditions: Computational Analysis with the Distortion/Interaction Model and Predictions of Reactivities.
‡9
1
|
919
|
|
|
‡a
bioorthogonalreleaseofsulfonamidesandmutuallyorthogonalliberationof2drugs
‡A
Bioorthogonal release of sulfonamides and mutually orthogonal liberation of two drugs
‡9
1
|
919
|
|
|
‡a
biosynthesisofstrainedpiperazinealkaloidsuncoveringtheconcisepathwayofherqulinea
‡A
Biosynthesis of Strained Piperazine Alkaloids - Uncovering the Concise Pathway of Herquline A.
‡9
1
|
919
|
|
|
‡a
controlanddesignofmutualorthogonalityinbioorthogonalcycloadditions
‡A
Control and design of mutual orthogonality in bioorthogonal cycloadditions
‡9
1
|
919
|
|
|
‡a
diazoestersasdienophilesinintramolecular
‡A
Diazo Esters as Dienophiles in Intramolecular
‡9
1
|
919
|
|
|
‡a
diazoestersasdienophilesinintramolecular4+2cycloadditionscomputationalexplorationsofmechanism
‡A
Diazo Esters as Dienophiles in Intramolecular (4 + 2) Cycloadditions: Computational Explorations of Mechanism.
‡9
1
|
919
|
|
|
‡a
dielsalderreactivitiesofbenzenepyridineand501triandtetrazinestherolesofgeometricaldistortionsandorbitalinteractions
‡A
Diels-Alder Reactivities of Benzene, Pyridine, and Di-, Tri-, and Tetrazines: The Roles of Geometrical Distortions and Orbital Interactions
‡9
1
|
919
|
|
|
‡a
dielsalderreactivitiesofstrainedandunstrainedcycloalkeneswithnormalandinverseelectrondemanddienesactivationbarriersanddistortioninteractionanalysis
‡A
Diels-Alder reactivities of strained and unstrained cycloalkenes with normal and inverse-electron-demand dienes: activation barriers and distortion/interaction analysis
‡9
1
|
919
|
|
|
‡a
holygrailsforcomputationalorganicchemistryandbiochemistry
‡A
Holy Grails for Computational Organic Chemistry and Biochemistry
‡9
1
|
919
|
|
|
‡a
isomerictriazinesexhibituniqueprofilesofbioorthogonalreactivity
‡A
Isomeric triazines exhibit unique profiles of bioorthogonal reactivity
‡9
1
|
919
|
|
|
‡a
molecularbasisforthefinaloxidativerearrangementstepsinchartreusinbiosynthesis
‡A
Molecular Basis for the Final Oxidative Rearrangement Steps in Chartreusin Biosynthesis
‡9
1
|
919
|
|
|
‡a
moleculardynamicsofthedielsalderreactionsoftetrazineswithalkenesandn2extrusionsfromadducts
‡A
Molecular dynamics of the Diels-Alder reactions of tetrazines with alkenes and N2 extrusions from adducts
‡9
1
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919
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‡a
originsofhalogeneffectsinbioorthogonalsydnonecycloadditions
‡A
Origins of halogen effects in bioorthogonal sydnone cycloadditions
‡9
1
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919
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‡a
reversiblephotochemicallygatedtransformationofahemicarcerandtoacarcerand
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Reversible photochemically gated transformation of a hemicarcerand to a carcerand
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1
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919
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|
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‡a
expandingworldofbiosyntheticpericyclasescooperationofexperimentandtheoryfordiscovery
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The expanding world of biosynthetic pericyclases: cooperation of experiment and theory for discovery
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1
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919
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theoreticalelucidationoftheoriginsofsubstituentandstraineffectsontheratesofdielsalderreactionsof1245tetrazines
‡A
Theoretical elucidation of the origins of substituent and strain effects on the rates of Diels-Alder reactions of 1,2,4,5-tetrazines
‡9
1
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|
‡2
BNF|14176250
|
996
|
|
|
‡2
ISNI|0000000382400990
|
996
|
|
|
‡2
NSK|000593725
|
996
|
|
|
‡2
ISNI|0000000382655221
|
996
|
|
|
‡2
NUKAT|n 2019070526
|
996
|
|
|
‡2
LC|nr 90002749
|
996
|
|
|
‡2
LC|nr 94022881
|
996
|
|
|
‡2
LC|n 84161878
|
996
|
|
|
‡2
DNB|1245903330
|
996
|
|
|
‡2
DNB|130082260
|
996
|
|
|
‡2
ISNI|0000000498412635
|
996
|
|
|
‡2
B2Q|0000691796
|
996
|
|
|
‡2
PLWABN|9812790795505606
|
996
|
|
|
‡2
CYT|AC000242536
|
996
|
|
|
‡2
NII|DA14405383
|
996
|
|
|
‡2
ISNI|0000000435969479
|
996
|
|
|
‡2
DNB|1129708152
|
996
|
|
|
‡2
ISNI|0000000064269130
|
996
|
|
|
‡2
CYT|AC000633255
|
996
|
|
|
‡2
CYT|AC000009238
|
996
|
|
|
‡2
BIBSYS|90303105
|
996
|
|
|
‡2
NUKAT|n 2022181688
|
996
|
|
|
‡2
DNB|1164455974
|
996
|
|
|
‡2
DNB|118768239X
|
996
|
|
|
‡2
LC|no2019113996
|
996
|
|
|
‡2
LC|no2024100379
|
996
|
|
|
‡2
ISNI|0000000063718555
|
996
|
|
|
‡2
PLWABN|9812744456705606
|
996
|
|
|
‡2
PLWABN|9810573341605606
|
996
|
|
|
‡2
LC|n 2014021986
|
996
|
|
|
‡2
LC|n 2013071534
|
996
|
|
|
‡2
DBC|87097991393387
|
996
|
|
|
‡2
PLWABN|9810554773105606
|
996
|
|
|
‡2
DNB|1011661764
|
996
|
|
|
‡2
ISNI|0000000063334914
|
996
|
|
|
‡2
CAOONL|ncf10287771
|
996
|
|
|
‡2
PLWABN|9811536907005606
|
996
|
|
|
‡2
LC|nr 92001841
|
996
|
|
|
‡2
LC|no2018040024
|
996
|
|
|
‡2
DNB|105689461X
|
996
|
|
|
‡2
LC|n 99265593
|
996
|
|
|
‡2
LC|n 87910564
|
996
|
|
|
‡2
ISNI|0000000420524207
|
996
|
|
|
‡2
ISNI|0000000072091619
|
996
|
|
|
‡2
LC|no2006110835
|
996
|
|
|
‡2
LC|n 2015057525
|
996
|
|
|
‡2
ISNI|0000000384798832
|
996
|
|
|
‡2
ISNI|0000000409435406
|
996
|
|
|
‡2
BIBSYS|1615358755453
|
996
|
|
|
‡2
LC|nr 97025678
|
996
|
|
|
‡2
ISNI|000000006346839X
|
996
|
|
|
‡2
DNB|120642334X
|
996
|
|
|
‡2
LC|no2021135011
|
996
|
|
|
‡2
J9U|987007437282905171
|
996
|
|
|
‡2
LC|n 83158795
|
996
|
|
|
‡2
DNB|1017813124
|
996
|
|
|
‡2
ISNI|0000000381505272
|
996
|
|
|
‡2
LC|n 85314944
|
996
|
|
|
‡2
ISNI|000000006349677X
|
996
|
|
|
‡2
CYT|AC000631568
|
996
|
|
|
‡2
NKC|jo2013796042
|
996
|
|
|
‡2
ISNI|0000000063549675
|
996
|
|
|
‡2
ISNI|0000000064372496
|
996
|
|
|
‡2
ISNI|0000000063888781
|
996
|
|
|
‡2
LC|n 85213853
|
996
|
|
|
‡2
ISNI|0000000382601039
|
996
|
|
|
‡2
ISNI|0000000053403744
|
996
|
|
|
‡2
ISNI|0000000359856498
|
997
|
|
|
‡a
0 0 lived 0 0
‡9
1
|
998
|
|
|
‡a
Fang, Liu
‡2
DNB|17175090X
‡3
exact name
|