About: Hideki Yorimitsu

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Hideki Yorimitsu (en) Hideki Yorimitsu (es) Hideki Yorimitsu (nl) Hideki Yorimitsu (sl) Hideki Yorimitsu (ast) 依光英樹 (ja)
skos:prefLabel	Hideki Yorimitsu (en) Hideki Yorimitsu (es) Hideki Yorimitsu (nl) Hideki Yorimitsu (sl) Hideki Yorimitsu (ast) 依光英樹 (ja)
name	Hideki Yorimitsu (en) Hideki Yorimitsu (es) Hideki Yorimitsu (nl) Hideki Yorimitsu (sl) Hideki Yorimitsu (ast) 依光英樹 (ja)
given name	wds:Q42797359-B032829D-26B2-4341-B074-9A4E0641221B
given name	Hideki
instance of	wds:Q42797359-FAE00ED6-CFD9-4510-BCFA-93CAC6D7CDF5
instance of	Homo sapiens
award received	wds:Q42797359-63b8de5c-46f1-6ab6-f534-19946ff4d678
award received	Mukaiyama Award
Researchmap ID	wds:Q42797359-07BE5F37-4350-4C9D-ADEC-F5B47CE174AD
Researchmap ID	read0192968
occupation	wds:Q42797359-3828ADF5-E599-46B9-83F0-B6B684D7324D
employer	wds:Q42797359-12544378-05DD-4F3F-88C8-643F2598BFD8 wds:Q42797359-166D8CFA-7277-4A7F-9151-483CDC078B13 wds:Q42797359-81E1BA39-A1AC-425E-B82B-98D7DCF6BD68 wds:Q42797359-C338D7E7-E7E7-48B8-AFCE-60783660D145
CiNii Research ID	wds:Q42797359-A5CE6CC4-227B-4C3C-A4B0-293D76D8AD28
sex or gender	wds:Q42797359-7D9EA52F-2C4F-4747-857E-6959B7F142D8
VIAF ID	wds:Q42797359-E26D13B7-BCA9-4C31-8BCD-E39F7F297811
GND ID	wds:q42797359-74e41fdc-4056-1700-9c85-1d81af88c40d
country of citizenship	wds:Q42797359-fbf01372-4eb4-83da-cb0a-fcc38dfb3f95
NACSIS-CAT author ID	wds:Q42797359-5E451F4C-0023-4EA2-BA43-48B1009FDD69
date of birth	wds:Q42797359-7A9FA2BF-88A4-4AF7-9FF6-A533C33D5C7B
educated at	wds:Q42797359-E24E3ABC-17E7-4B79-B3A8-64839AFC15D9
J-GLOBAL ID	wds:Q42797359-2822c56f-47ff-5bac-2791-aac987a2524a
CiNii Research ID	https://cir.nii.ac.jp/crid/1420845751146161152.rdf
VIAF ID	http://viaf.org/viaf/441146997241918890829
GND ID	https://d-nb.info/gnd/1261064003
NACSIS-CAT author ID	https://ci.nii.ac.jp/author/DA17600545#entity
occupation	researcher
employer	National Taipei University of Technology Kyoto University Institute for Molecular Science
CiNii Research ID	1420845751146161152
sex or gender	male
VIAF ID	441146997241918890829
GND ID	1261064003
country of citizenship	Japan
NACSIS-CAT author ID	DA17600545
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
educated at	Kyoto University
J-GLOBAL ID	200901099345424118
ORCID iD	wds:Q42797359-4674ADD3-5F41-4ECC-BB6A-4D0AAFB89FF1
ORCID iD	https://orcid.org/0000-0002-0153-1888
ORCID iD	0000-0002-0153-1888
e-Rad researcher number	wds:Q42797359-81F2D702-B039-4B6A-9FF1-00F440422771
e-Rad researcher number	00372566
ResearcherID	wds:Q42797359-FC504702-CAE3-4092-BD95-E6C025B9C715
Publons author ID	wds:Q42797359-eddf42d2-a307-4286-8c50-0dc8dba988d1
ResearcherID	C-2451-2011
Publons author ID	2804407
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42797359
is author of	Stereoselective hydrothiolation of alkynes catalyzed by cesium base: facile access to (Z)-1-alkenyl sulfides. Palladium-catalyzed anti-hydrothiolation of 1-alkynylphosphines. Recent progress in asymmetric allylic substitutions catalyzed by chiral copper complexes. Palladium-catalyzed benzylic arylation of N-benzylxanthone imine. Selective deposition of a gadolinium(III) cluster in a hole opening of single-wall carbon nanohorn. Synthesis of 3-trifluoromethylbenzo[b]furans from phenols via direct ortho functionalization by extended Pummerer reaction Reaction of 2-(2,2,2-trifluoroethylidene)-1,3-dithiane 1-oxide with ketones under Pummerer conditions and its application to the synthesis of 3-trifluoromethyl-substituted five-membered heteroarenes Synthesis of benzo[b]thiophenes by cyclization of arylketene dithioacetal monoxides under pummerer-like conditions. Rhodium-catalyzed allylation of aldehydes with homoallylic alcohols by retroallylation and isomerization to saturated ketones with conventional or microwave heating. 1-Alkynylphosphines and their derivatives as key starting materials in creating new phosphines. Palladium-catalyzed direct arylation of aryl(azaaryl)methanes with aryl halides providing triarylmethanes. Palladium-catalyzed 2-pyridylmethyl transfer from 2-(2-pyridyl)ethanol derivatives to organic halides by chelation-assisted cleavage of unstrained C(sp3 )--C(sp3) bonds. Nickel-catalysed reactions with trialkylboranes and silacyclobutanes Nickel-catalyzed beta-boration of alpha,beta-unsaturated esters and amides with bis(pinacolato)diboron. Transformation of zirconocene-olefin complexes into zirconocene allyl hydride and their use as dual nucleophilic reagents: reactions with acid chloride and 1,4-diketone. Silver-catalyzed transmetalation between chlorosilanes and aryl and alkenyl Grignard reagents for the synthesis of tetraorganosilanes. Nickel-catalyzed borylation of aryl cyclopropyl ketones with bis(pinacolato)diboron to synthesize 4-oxoalkylboronates Synthesis of aziridines by palladium-catalyzed reactions of allylamines with aryl and alkenyl halides: evidence of a syn-carboamination pathway Nickel-catalyzed borylative ring-opening reaction of vinylcyclopropanes with bis(pinacolato)diboron yielding allylic boronates

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