about
Transition Metal-Free Tryptophan-Selective Bioconjugation of ProteinsTargeting Ras-Driven Cancer Cell Survival and Invasion through Selective Inhibition of DOCK1.Catalytic migratory oxidative coupling of nitrones through an outer-sphere C(sp3)-H activation process.Identification of modular chiral bisphosphines effective for Cu(i)-catalyzed asymmetric allylation and propargylation of ketones.Catalytic enantioselective allylboration of ketones.A metal-organic framework with covalently bound organometallic complexes.Manganese-catalyzed aerobic dehydrogenative cyclization toward ring-fused indole skeletons.Asymmetric reductive Mannich reaction to ketimines catalyzed by a Cu(I) complex.Directing activator-assisted regio- and oxidation state-selective aerobic oxidation of secondary C(sp(3))-H bonds in aliphatic alcohols.Crystalline covalent organic frameworks with hydrazone linkages.Sulfonamides as new hydrogen atom transfer (HAT) catalysts for photoredox allylic and benzylic C-H arylations.DOCK1 inhibition suppresses cancer cell invasion and macropinocytosis induced by self-activating Rac1P29S mutation.Switchable photooxygenation catalysts that sense higher-order amyloid structures.C(sp3 )-H Cyanation Promoted by Visible-Light Photoredox/Phosphate Hybrid Catalysis.Chemo- and regioselective oxygenation of C(sp3)-H bonds in aliphatic alcohols using a covalently bound directing activator and atmospheric oxygen.A catalytic one-step synthesis of peptide thioacids: the synthesis of leuprorelin via iterative peptide-fragment coupling reactionsA new method for the catalytic aldol reaction to ketonesDramatic ligand effect in catalytic asymmetric reductive aldol reaction of allenic esters to ketonesCu(I)-catalyzed hetero-Diels-Alder reaction between Danishefsky-type siloxy dienes and ketonesCatalytic enantioselective alkylative aldol reaction: efficient multicomponent assembly of dialkylzincs, allenic esters, and ketones toward highly functionalized delta-lactones with tetrasubstituted chiral centersCatalytic enantioselective aldol reaction to ketonesCatalytic enantioselective allylation of ketoiminesFunctional-group-tolerant catalytic migratory oxidative coupling of nitronesCatalytic migratory oxidative coupling of nitronesIron-catalyzed oxidative C(3)-H functionalization of aminesMetal-free C(3)-H arylation of coumarins promoted by catalytic amounts of 5,10,15,20-tetrakis(4-diethylaminophenyl)porphyrinEnhanced Structural Variety of Nonplanar N-Oxyl Radical Catalysts and Their Application to the Aerobic Oxidation of Benzylic C-H BondsSerine-selective aerobic cleavage of peptides and a protein using a water-soluble copper-organoradical conjugate
P50
Q27727706-A81BCF72-EE58-43E6-A420-EC4FE1E6F068Q36362143-B49078CC-CE41-4EB5-9202-56D7488C13CEQ37928616-B44AEEB5-37F2-4AB2-A20E-DE7B25BBF4EEQ43085353-BE0ADCAE-DE75-45EF-ADDD-F01AE3B7DFC1Q44986285-68FF6618-9BFF-46EE-AF97-51F29B1A8FDEQ46078277-505DD8DC-70CE-463E-B3EA-2FFFFD775411Q46175648-4D7D55CE-02DA-4922-A4A5-2B7B3651646CQ46254469-62C39800-E90B-4F97-95B6-B655F650744BQ46558866-65C85AC0-8095-4DF1-BEC5-7E2A921A6493Q46691399-A1C4DB20-2204-4B91-8841-67CBFEB44644Q48116160-8D3B77E5-7971-42A3-83A7-ECF86DD090EAQ50060966-09A79A64-0A2C-4161-A06B-0F03F15E677AQ51474859-010DECAC-B720-4CD6-9D99-4BA5A964BDE2Q52719876-9790B3E0-3B07-42DB-A9F5-917A91FECC98Q55287312-704EF6CD-40F5-4828-A287-09FAA3852FF4Q57470624-31B93530-FE95-4189-A5C1-D9923C5DDB45Q73359696-E4C4F480-F8C1-4771-BD6E-28D2F2DD1508Q79336366-09932E83-2787-4850-90A0-155BE1582B8EQ79719524-82B58BD1-D817-4B3A-B896-076B7AF4ED74Q80339103-8FF2E891-E9A2-4993-A101-225F9439517DQ83874557-8EA53C8A-CF89-48DA-82E6-4566E45E76AAQ83934933-F11E31F9-A4FA-435A-9944-205BB08A2E50Q84524153-17FE77AD-58C8-494F-8579-CD426DB17818Q84568756-7D6C5030-7550-46F8-9E5B-FDBBFDD14487Q86579172-B9C9E934-75C1-46FD-8972-287A0A5C6BBEQ87324242-6E920DBB-1278-43B7-884E-776E2C117717Q87810651-5FE15622-58B1-4E09-8E80-5CA7B2360712Q87872902-F80694E3-9A23-4076-90BA-180A9A22B480
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kounosuke Oisaki
@ast
Kounosuke Oisaki
@en
Kounosuke Oisaki
@es
Kounosuke Oisaki
@nl
type
label
Kounosuke Oisaki
@ast
Kounosuke Oisaki
@en
Kounosuke Oisaki
@es
Kounosuke Oisaki
@nl
prefLabel
Kounosuke Oisaki
@ast
Kounosuke Oisaki
@en
Kounosuke Oisaki
@es
Kounosuke Oisaki
@nl
P106
P31
P496
0000-0002-0499-8168