about
Preparation, structure, and unique thermal [2+2], [4+2], and [3+2] cycloaddition reactions of 4-vinylideneoxazolidin-2-one.Chelating bis(thiophosphinic amidate)s as versatile supporting ligands for the group 3 metals. An application to the synthesis of highly active catalysts for intramolecular alkene hydroamination.Pd(0)-catalyzed amphiphilic activation of bis-allyl alcohol and ether.Gold-catalyzed intermolecular addition of alcohols toward the allenic bond of 4-vinylidene-2-oxazolidinones.Stereoselective synthesis of vinylsilanes by a gold(I)-catalyzed acetylenic sila-cope rearrangement.Synthesis of Potent and Selective Inhibitors of Aldo-Keto Reductase 1B10 and Their Efficacy against Proliferation, Metastasis, and Cisplatin Resistance of Lung Cancer Cells.Pd(0)-catalyzed amphiphilic allylation of aldehydes with vinyl epoxide.Rhenium-catalyzed C-H and C-C bond activation.Site-selective chemical modification of chymotrypsin using peptidyl derivatives bearing optically active diphenyl 1-amino-2-phenylethylphosphonate: Stereochemical effect of the diphenyl phosphonate moiety.Practical and convenient synthesis of 1,6-di- or 1,2,5,6-tetra-arylhexa-1,3,5-trienes by the dimerization of Pd(0)-complexed alkenylcarbenes generated from π-allylpalladium intermediates.Facile preparation of dehydrodigallic acid and its derivative for the synthesis of ellagitannins.Chameleon reactivity of the allene bond of 4-vinylidene-2-oxazolidinone: novel through-space conjugative nucleophilic addition of electron-rich alkenes and hetero-nucleophilesPd-Catalyzed Three-Component Reaction of 3-(Pinacolatoboryl)ally Acetates, Aldehydes, and Organoboranes: A New Entry to Stereoselective Synthesis of (Z)-anti-Homoallylic AlcoholsControllable Stereoselective Synthesis of (Z)- and (E)-Homoallylic Alcohols Using a Palladium-Catalyzed Three-Component ReactionTrialkylborane-Mediated Multicomponent Reaction for the Diastereoselective Synthesis of Anti-δ,δ-Disubstituted Homoallylic AlcoholsTrialkylborane-Mediated Propargylation of Aldehydes Using γ-Stannylated Propargyl AcetatesDMSO-Perturbing Assay for Identifying Promiscuous Enzyme Inhibitors
P50
Q44470664-48984188-64A4-4C46-8323-AE205419778CQ44540110-34D2D1F0-0A67-44A5-8B50-C1D04605B0D1Q45049767-C4578BE7-79F0-4094-A19F-CC7CA317AFCBQ46275070-E57B078D-D36B-4A4A-9AB6-FCB1A62E7CA4Q46314365-3A1D6FE3-91D1-4981-826A-4BC86061D3F6Q47602500-BDB2DBE6-E861-4284-A83D-4F3423246BA9Q51042854-E132F22F-0EDF-4D62-AB5A-E6A48D5E21E9Q51059221-FBAC7231-55D2-46FF-8E16-AFAAB0B680CBQ51626000-212F65FA-31D3-4996-9E43-96961A8F36F3Q53527343-6FBCC64B-E559-4A8D-ADBB-E951FAFFB453Q53662221-750FBD5D-93A1-44D9-8D4B-C71C34C487E9Q80985533-8CAA6C13-5EAB-4DE1-945D-B66D741F7555Q87354018-F7FA3B77-423C-4AD1-82CC-447326C44097Q89721454-29CE52DE-9B92-48A2-A587-F341B6609CD1Q90819842-3946C947-90E7-4AD0-ACF5-6E8B5D829610Q91461097-32D77034-9F7E-42ED-AA71-22DB96A24333Q92929507-F2C7AF4B-AE70-48F3-8AEB-5497901BA53C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Yoshikazu Horino
@ast
Yoshikazu Horino
@en
Yoshikazu Horino
@es
Yoshikazu Horino
@nl
Yoshikazu Horino
@sl
type
label
Yoshikazu Horino
@ast
Yoshikazu Horino
@en
Yoshikazu Horino
@es
Yoshikazu Horino
@nl
Yoshikazu Horino
@sl
prefLabel
Yoshikazu Horino
@ast
Yoshikazu Horino
@en
Yoshikazu Horino
@es
Yoshikazu Horino
@nl
Yoshikazu Horino
@sl
P1053
G-6212-2013
P106
P1153
7006394420
P21
P31
P3829
P3835
yoshikazu-horino
P496
0000-0002-8916-6298
P569
2000-01-01T00:00:00Z