About: Sukbok Chang

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South Korean chemist

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) দক্ষিণ কোরীয় রসায়নবিদ (bn) Lõuna-Korea keemik (et) South Korean chemist (en) chimist sud-coreean (ro) chimiste sud-coréen (fr) kimist koreano-jugor (sq) químic sud-coreà (ca) químico surcoreano (es) químico surcoreano (gl) כימאי דרום קוריאני (he) كيميائي كوري جنوبي (ar) químicu surcoreanu (ast)
rdfs:label	Sukbok Chang (en) Sukbok Chang (es) Sukbok Chang (nl) Sukbok Chang (sq) Sukbok Chang (ast) 장석복 (ko)
skos:prefLabel	Sukbok Chang (en) Sukbok Chang (es) Sukbok Chang (nl) Sukbok Chang (sq) Sukbok Chang (ast) 장석복 (ko)
name	Sukbok Chang (en) Sukbok Chang (es) Sukbok Chang (nl) Sukbok Chang (sq) Sukbok Chang (ast) 장석복 (ko)
given name	wds:Q16880404-B065AE0E-1AAD-48DE-A652-EFACB1E1C5E9
given name	Seok-bok
image	wds:Q16880404-958b67ca-4fa2-2ac4-fe7b-4ba35d9df846
instance of	wds:Q16880404-7427e78d-4ab7-4590-2655-86b1b3324391
image
instance of	Homo sapiens
award received	wds:Q16880404-31D53BAE-4A5B-4758-A180-03D74689CE06
award received	Korea Science Award
Google Knowledge Graph ID	wds:Q16880404-0D960C80-8CBF-42B3-A50C-7F1391D4C8D0
Google Knowledge Graph ID	http://g.co/kg/g/1s0524zs2
Google Knowledge Graph ID	/g/1s0524zs2
Google Scholar author ID	wds:Q16880404-8c1ab3fd-43d4-7339-e6d0-100070510b94
Google Scholar author ID	z3-v1EwAAAAJ
Commons category	wds:Q16880404-9b55c5c3-1363-4a93-b585-01d27f315405
Commons category	Sukbok Chang
skos:altLabel	Chang Sukbok (en)
occupation	wds:Q16880404-bd28ba2a-9fee-4f74-8d9e-e05ddeeaf616
employer	wds:Q16880404-80e04a56-ae32-4b15-9e4c-df75e5f53197
sex or gender	wds:Q16880404-449897D2-FBCD-4155-9AF6-2B87CFAAECDC
ISNI	wds:Q16880404-be9d3bfb-4171-997c-aa24-b9ec003db519
VIAF ID	wds:Q16880404-694f6d69-4022-2fe3-0959-af5be0f89bb2
country of citizenship	wds:Q16880404-0a97f59b-4250-3108-40b6-9f9dd8e7a390
National Library of Korea ID	wds:Q16880404-72318fc1-4b17-c405-3455-428a3059497c
date of birth	wds:Q16880404-B77C4D6B-065F-4E78-BCF0-FEECA2F70415
educated at	wds:Q16880404-14aa6a1a-18f0-404c-9a19-f14a2c9389e7
WorldCat Identities ID (superseded)	wds:Q16880404-5AFD510F-1C71-48DA-97E0-0B519916B324
VIAF ID	http://viaf.org/viaf/383155103916776200940
National Library of Korea ID	http://lod.nl.go.kr/resource/KAC2018M0347
occupation	chemist
employer	KAIST
sex or gender	male
ISNI	0000000473818807
VIAF ID	383155103916776200940
country of citizenship	Korea
National Library of Korea ID	KAC2018M0347
date of birth	1962-08-01 00:00:00Z (xsd:dateTime)
educated at	Harvard University
WorldCat Identities ID (superseded)	viaf-383155103916776200940
ORCID iD	wds:Q16880404-DBBF1800-6BB3-4108-940D-02D55ECD7F24
ORCID iD	https://orcid.org/0000-0001-9069-0946
ORCID iD	0000-0001-9069-0946
ResearcherID	wds:Q16880404-445716C3-3449-4B65-A82E-830ED6661518
ResearcherID	C-1594-2011
is owl:sameAs of	Sukbok Chang
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q16880404 Sukbok Chang Category:Sukbok Chang https://ko.wikipedia.org/wiki/%EC%9E%A5%EC%84%9D%EB%B3%B5
is author of	Copper-catalyzed hydrative amide synthesis with terminal alkyne, sulfonyl azide, and water Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation Intramolecular oxidative C-N bond formation for the synthesis of carbazoles: comparison of reactivity between the copper-catalyzed and metal-free conditions Rh-catalyzed one-pot and practical transformation of aldoximes to amides. [Cu(NHC)]-Catalyzed C-H Allylation and Alkenylation of both Electron-Deficient and Electron-Rich (Hetero)arenes with Allyl Halides Recent advances in olefin metathesis and its application in organic synthesis Palladium-catalyzed C-H functionalization of pyridine N-oxides: highly selective alkenylation and direct arylation with unactivated arenes [RuCl(2)(p-cymene)](2) on carbon: an efficient, selective, reusable, and environmentally versatile heterogeneous catalyst Rhodium-catalyzed selective olefination of arene esters via C-H bond activation Acetone cyanohydrin as a source of HCN in the Cu-catalyzed hydrocyanation of alpha-aryl diazoacetates Copper-mediated sequential cyanation of aryl C-B and arene C-H bonds using ammonium iodide and DMF Ruthenium-catalyzed Heck-type olefination and Suzuki coupling reactions: studies on the nature of catalytic species Cooperative multi-catalyst systems for one-pot organic transformations Highly efficient one-pot synthesis of N-sulfonylamidines by Cu-catalyzed three-component coupling of sulfonyl azide, alkyne, and amine Copper-catalyzed synthesis of N-sulfonyl-1,2,3-triazoles: controlling selectivity Mechanistic studies on the Cu-catalyzed three-component reactions of sulfonyl azides, 1-alkynes and amines, alcohols, or water: dichotomy via a common pathway Transition-metal-catalyzed C-N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C-H amination A new combined source of "CN" from N,N-dimethylformamide and ammonia in the palladium-catalyzed cyanation of aryl C-H bonds Synthesis of aromatic nitriles using nonmetallic cyano-group sources

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