About: Kuiling Ding

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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	forskare (sv) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Kuiling Ding (en) Kuiling Ding (es) Kuiling Ding (nl) Kuiling Ding (ast)
skos:prefLabel	Kuiling Ding (en) Kuiling Ding (es) Kuiling Ding (nl) Kuiling Ding (ast)
name	Kuiling Ding (en) Kuiling Ding (es) Kuiling Ding (nl) Kuiling Ding (ast)
Scopus author ID	wds:Q56452547-CEC998E5-4AEB-42C6-A663-8CCBF41CAE7C
Scopus author ID	7103198017
instance of	wds:Q56452547-E26FA152-CD1F-4705-8234-F0DB1B6C4595
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q56452547-8c53d67b-0237-4c8f-a2de-c13d5d28412c
occupation	wds:Q56452547-E80F82B3-29F9-44FB-BAFA-BB61E2E4F661
employer	wds:Q56452547-FC9B0145-8750-49B3-BB18-3AFE8064CB51
NUKAT ID	wds:Q56452547-CD7AB444-2864-4961-8991-4077067AAC2A
sex or gender	wds:Q56452547-5631AC9A-F1B4-447C-8758-385E65AE7531
ISNI	wds:Q56452547-FA95B8AC-2D32-466F-BFE6-FAC6B57364F8
VIAF ID	wds:Q56452547-0052AD70-01D1-491D-B06E-FD98115F91FB
GND ID	wds:Q56452547-04ccd9ac-cf32-401a-9587-28b7ce5f01cc
Library of Congress authority ID	wds:Q56452547-21E7F7D7-914C-45F0-9970-885A5D0FC523
IdRef ID	wds:Q56452547-E4A7CB82-D695-4F0C-92E4-4AEC7C392AC7
date of birth	wds:Q56452547-C9610026-1A1F-415F-B077-1E8B04C88B72
educated at	wds:Q56452547-36DA8C17-3EDB-4989-B7DC-5DD7DAC45C35
WorldCat Identities ID (superseded)	wds:Q56452547-5C6A967C-0607-45C9-B5F9-F5FF0085E0AB
National Library of Israel J9U ID	wds:Q56452547-E27D8C26-D03A-4645-A0CC-E6876FA70282
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p352647590
VIAF ID	http://viaf.org/viaf/26599368
GND ID	https://d-nb.info/gnd/136290655
Library of Congress authority ID	http://id.loc.gov/authorities/names/nb2008020552
IdRef ID	http://www.idref.fr/130292494/id
Nationale Thesaurus voor Auteursnamen ID	352647590
occupation	researcher
employer	Shanghai Institute of Organic Chemistry
NUKAT ID	n2009167579
sex or gender	male
ISNI	0000000116105307
VIAF ID	26599368
GND ID	136290655
Library of Congress authority ID	nb2008020552
IdRef ID	130292494
date of birth	1966-01-01 00:00:00Z (xsd:dateTime)
educated at	Nanjing University
WorldCat Identities ID (superseded)	lccn-nb2008020552
National Library of Israel J9U ID	987007423689205171
ORCID iD	wds:Q56452547-F62A35BD-09D7-4F25-BB75-7E6F7B43B770
ORCID iD	https://orcid.org/0000-0003-4074-1981
ORCID iD	0000-0003-4074-1981
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56452547
is author of	Enantioselective catalysis of the hetero-Diels-Alder reaction between Brassard's diene and aldehydes by hydrogen-bonding activation: a one-step synthesis of (S)-(+)-dihydrokawain. Copolymerization of cyclohexene oxide with CO2 by using intramolecular dinuclear zinc catalysts. Highly enantioselective Friedel-Crafts reaction of aromatic amines with ethyl glyoxylate catalyzed by chiral titanium(IV) complexes: practical synthesis of aminomandelic acid derivatives. Experimental and theoretical studies on the hydrogen-bond-promoted enantioselective hetero-Diels-Alder reaction of Danishefsky's diene with benzaldehyde Hydrogen bonding makes a difference in the rhodium-catalyzed enantioselective hydrogenation using monodentate phosphoramidites Highly enantioselective asymmetric hydrogenation of (E)-β,β-disubstituted α,β-unsaturated Weinreb amides catalyzed by Ir(I) complexes of SpinPhox ligands Discovery of exceptionally efficient catalysts for solvent-free enantioselective hetero-Diels-Alder reaction. An efficient titanium catalyst for enantioselective cyanation of aldehydes: cooperative catalysis. Mechanistic investigation of chiral phosphoric acid catalyzed asymmetric Baeyer-Villiger reaction of 3-substituted cyclobutanones with H2O2 as the oxidant. Catalytic hydrogenation of cyclic carbonates: a practical approach from CO2 and epoxides to methanol and diols Highly Efficient Ruthenium-Catalyzed N-Formylation of Amines with H₂ and CO₂ Highly stereoselective olefin cyclopropanation of diazooxindoles catalyzed by a C2-symmetric spiroketal bisphosphine/Au(I) complex. Insight into the mechanism of the asymmetric ring-opening aminolysis of 4,4-dimethyl-3,5,8-trioxabicyclo[5.1.0]octane catalyzed by titanium/BINOLate/water system: evidence for the Ti(BINOLate)2-bearing active catalyst entities and the role of water. Modular chiral bidentate phosphonites: design, synthesis, and application in catalytic asymmetric hydroformylation reactions Facile preparation of alpha-aryl nitriles by direct cyanation of alcohols with TMSCN under the catalysis of InX3 Spiro skeletons: a class of privileged structure for chiral ligand design. Enantioselective palladium-catalyzed diboration of 1,1-disubstituted allenes Spiroketal-based diphosphine ligands in Pd-catalyzed asymmetric allylic amination of Morita-Baylis-Hillman adducts: exceptionally high efficiency and new mechanism. Highly Regio- and Enantioselective Alkoxycarbonylative Amination of Terminal Allenes Catalyzed by a Spiroketal-Based Diphosphine/Pd(II) Complex. Aromatic spiroketal bisphosphine ligands: palladium-catalyzed asymmetric allylic amination of racemic Morita-Baylis-Hillman adducts One-pot enantioselective aziridination of olefins catalyzed by a copper(I) complex of a novel diimine ligand by using PhI(OAc)(2) and sulfonamide as nitrene precursors Acid-Free Aza Diels−Alder Reaction of Danishefsky's Diene with Imines The N-H functional group in organometallic catalysis. Self-supported catalysts Development of a continuous-flow system for asymmetric hydrogenation using self-supported chiral catalysts. Catalytic asymmetric hydrogenation of α-CF3- or β-CF3-substituted acrylic acids using rhodium(I) complexes with a combination of chiral and achiral ligands. Spiro[4,4]-1,6-nonadiene-based phosphine-oxazoline ligands for iridium-catalyzed enantioselective hydrogenation of ketimines. Rhodium-Complex-Catalyzed Hydroformylation of Olefins with CO2 and Hydrosilane. Engineering a polymeric chiral catalyst by using hydrogen bonding and coordination interactions. Design, synthesis, biological evaluation and cocrystal structures with tubulin of chiral β-lactam bridged combretastatin A-4 analogues as potent antitumor agents. Direct on-line method to monitor the dynamic structure of noncovalent titanium complexes in solution by using cold-spray ionization time-of-flight mass spectrometry. Chiral Brønsted acid catalyzed asymmetric Baeyer-Villiger reaction of 3-substituted cyclobutanones by using aqueous H2O2 Programmed assembly of two different ligands with metallic ions: generation of self-supported Noyori-type catalysts for heterogeneous asymmetric hydrogenation of ketones Spiroketal-based phosphorus ligands for highly regioselective hydroformylation of terminal and internal olefins

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