about
BN isosteres of indoleStructural Characterization and Computer-Aided Optimization of a Small-Molecule Inhibitor of the Arp2/3 Complex, a Key Regulator of the Actin CytoskeletonHydrogen Bonding of 1,2-Azaborines in the Binding Cavity of T4 Lysozyme Mutants: Structures and ThermodynamicsRhodium-catalyzed B-H activation of 1,2-azaborines: synthesis and characterization of BN isosteres of stilbenes.Electrophilic aromatic substitution of a BN indole.UV-photoelectron spectroscopy of BN indoles: experimental and computational electronic structure analysis1,2-Azaborine cationsA hybrid organic/inorganic benzene.A 1,3-dihydro-1,3-azaborine debuts.1,2-Azaborine: The Boron-Nitrogen Derivative of ortho-BenzyneUV-photoelectron spectroscopy of 1,2- and 1,3-azaborines: a combined experimental and computational electronic structure analysisNucleophilic aromatic substitution reactions of 1,2-dihydro-1,2-azaborine.Photoisomerization of 1,2-dihydro-1,2-azaborine: a matrix isolation study.The Synthesis, Characterization and Dehydrogenation of Sigma-Complexes of BN-Cyclohexanes.Protecting group-free synthesis of 1,2-azaborines: a simple approach to the construction of BN-benzenoidsRhodium-catalyzed boron arylation of 1,2-azaborinesBoron-substituted 1,3-dihydro-1,3-azaborines: synthesis, structure, and evaluation of aromaticity.A single-component liquid-phase hydrogen storage material.Graphene-like Boron-Carbon-Nitrogen Monolayers.Thermodynamically Controlled, Dynamic Binding of Diols to a 1,2-BN Cyclohexane Derivative.Negishi Cross-Coupling Is Compatible with a Reactive B-Cl Bond: Development of a Versatile Late-Stage Functionalization of 1,2-Azaborines and Its Application to the Synthesis of New BN Isosteres of Naphthalene and Indenyl.Hydrogen storage by boron-nitrogen heterocycles: a simple route for spent fuel regeneration.Dehydrogenation reactions of cyclic C(2)B(2)N(2)H(12) and C(4)BNH(12) isomers.BN benzonitrile: an electron-deficient 1,2-dihydro-1,2-azaborine featuring linkage isomerism.Microwave measurements and ab initio calculations of structural and electronic properties of N-Et-1,2-azaborine.Site-Selective and Stereoselective trans-Hydroboration of 1,3-Enynes Catalyzed by 1,4-Azaborine-Based Phosphine-Pd Complex.Microwave spectrum, structural parameters, and quadrupole coupling for 1,2-dihydro-1,2-azaborine.The State of the Art in Azaborine Chemistry: New Synthetic Methods and Applications.Synthesis of 1,2-Azaborines and the Preparation of Their Protein Complexes with T4 Lysozyme Mutants.The Least Stable Isomer of BN Naphthalene: Toward Predictive Trends for the Optoelectronic Properties of BN Acenes.Synthesis by free radical polymerization and properties of BN-polystyrene and BN-poly(vinylbiphenyl).A Boron Protecting Group Strategy for 1,2-Azaborines.The Dewar isomer of 1,2-dihydro-1,2-azaborinines: Isolation, fragmentation, and energy storage.Medicinal Chemistry Profiling of Monocyclic 1,2-Azaborines.Two BN isosteres of anthracene: synthesis and characterization.Monobenzofused 1,4-azaborines: synthesis, characterization, and discovery of a unique coordination mode.Diels-Alder Reactions of 1,2-Azaborines.Crystal clear structural evidence for electron delocalization in 1,2-dihydro-1,2-azaborines.Charge-Transfer-Induced Magic Cluster Formation of Azaborine Heterocycles on Noble Metal SurfacesEffect of BN/CC Isosterism on the Thermodynamics of Surface and Bulk Binding: 1,2-Dihydro-1,2-azaborine vs Benzene
P50
Q26863690-4EB1F3B8-B891-4C68-B16A-4E96F2E26590Q27679277-FEB1E531-040A-4835-80D8-0FF8951A3229Q27728018-1D861394-8435-4157-A9B6-D7DCCF1C2602Q30830236-7E5E199D-6154-4AB8-87F8-AB3EADFD7A79Q33736194-2D1CF7D1-2FA3-4F36-9F8A-2976F92333A4Q34074542-3692BC80-F9D9-4AEC-B220-B7661CE27123Q34787943-E7A1AD97-56C6-4973-9B08-D29F7C55F941Q34910054-6C0BBEC8-CF28-45ED-834E-A8918D40440CQ35621445-6DB1065A-EDB8-4925-AC32-DB640B090195Q36045349-338A8C20-071E-41AB-8DCB-90AC3FC5A4DEQ36049313-061CACCF-51B1-4DA5-A774-B9BB8EF62CD8Q36219987-34F1ACD8-ED0F-49FC-8BDE-9A503CF77734Q36452751-7C2CE643-AD42-4E0C-840A-F3A1888EF31AQ36760068-D9683FD7-9900-47D6-991A-BD80546407ECQ37257533-1169C380-ABDD-4383-BA8D-7A070B408BEBQ37257567-4A73BE75-591B-4EEC-80B6-0C05FD591363Q37268994-6F52A9F9-F667-4DF0-88A9-3C9B030F4B4DQ38420053-8A535A1E-47F5-4836-BD86-DA25EEF887DFQ38976862-B95EB774-3C47-45DD-A187-5172BE1B0F6FQ41180749-24528745-6B94-431F-9CC7-92FD55168D9FQ41873259-AF7E6294-602D-4FEB-90B8-DD2FABBE223BQ43137261-3C8A6DB5-F671-49D5-940D-7C78A94D6CB5Q43180707-9128B7E6-EECE-459A-A707-252E3EA9F185Q43189171-27B31E58-9634-4483-9CDB-44C4BE41EE64Q43225918-310645F5-B2B8-4ABD-AFCC-880850C04629Q43397112-AAA02B7B-5F5F-417A-A6BD-85FE54D98655Q45194613-B45D8EA4-67DF-47F1-9F08-478447B57943Q47743829-6993671F-6D1E-440D-AAD4-EA2DE12EB631Q47798823-2CAD555E-E1D6-4AD2-BF45-87BB8E643067Q48063350-2C6E2F9E-6958-4225-BF30-B4B2CC98E4A7Q48246228-DF346DA0-51E0-4857-9A7F-D13AE2060A2BQ48260019-F75666DF-F817-475E-A96A-DEFD0A4804AEQ49852042-6D6FC207-0D64-40DB-972F-AA8AD506D9E0Q50902844-F9299CF7-6E47-4370-B6F5-AD17EEB0B730Q51047793-AD597697-F99E-4160-8ECE-399206812D1DQ51734399-F6DEEF3A-A0FC-4B58-BB4C-60A88F262328Q53658919-65C794BF-64BE-452C-AB63-1CBD62BB83D5Q53934155-5D8FCEC5-CFEF-4D65-8BD7-541604FDE0B9Q56992988-56D16BB5-6A84-4116-8AD3-034EC684D67CQ56993025-76B5B59D-46F5-493D-8D14-714FA06C3F98
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Shih-Yuan Liu
@ast
Shih-Yuan Liu
@en
Shih-Yuan Liu
@es
Shih-Yuan Liu
@nl
Shih-Yuan Liu
@sl
type
label
Shih-Yuan Liu
@ast
Shih-Yuan Liu
@en
Shih-Yuan Liu
@es
Shih-Yuan Liu
@nl
Shih-Yuan Liu
@sl
prefLabel
Shih-Yuan Liu
@ast
Shih-Yuan Liu
@en
Shih-Yuan Liu
@es
Shih-Yuan Liu
@nl
Shih-Yuan Liu
@sl
P106
P31
P496
0000-0003-3148-9147