About: Nicolai Cramer

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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) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Nicolai Cramer (en) Nicolai Cramer (es) Nicolai Cramer (nl) Nicolai Cramer (sl) Nicolai Cramer (ast)
skos:prefLabel	Nicolai Cramer (en) Nicolai Cramer (es) Nicolai Cramer (nl) Nicolai Cramer (sl) Nicolai Cramer (ast)
name	Nicolai Cramer (en) Nicolai Cramer (es) Nicolai Cramer (nl) Nicolai Cramer (sl) Nicolai Cramer (ast)
Scopus author ID	wds:Q43166481-41E2AFB7-6BC7-4B31-9E18-31B4A1701CD1
Scopus author ID	7006739893
given name	wds:Q43166481-C3910B42-7AFB-45E2-97EC-B25AA78DE8E7
given name	Nicolai
instance of	wds:Q43166481-90C121D3-8DE2-46CC-A14D-D90C61DD8807
instance of	Homo sapiens
award received	wds:Q43166481-63624A27-D172-4FEE-A5DD-0E00FFA3EA79
award received	ORCHEM-Award
Academic Tree ID	wds:Q43166481-ADB8732B-94E1-4207-8353-96753F0EBA0F
Academic Tree ID	72294
Nationale Thesaurus voor Auteursnamen ID	wds:Q43166481-abd4226d-4471-4df3-861a-fd2da500272b
occupation	wds:Q43166481-C13AC949-555C-43D5-8051-275AA21CAC2A
employer	wds:Q43166481-71136F18-F42C-4EFF-B82B-F71F0E05CA78
NUKAT ID	wds:Q43166481-4D636C7B-7F61-425F-B21E-A86CB3B2134F
sex or gender	wds:Q43166481-0D39C943-7DCD-40B8-8203-591BA3C82ECC
ISNI	wds:Q43166481-77EEA5C1-B367-4817-9692-B6A435759260
VIAF ID	wds:Q43166481-431432D6-EB0E-489A-8EC2-D43732A99CF1
GND ID	wds:q43166481-092c48bc-41ab-00b6-cfb1-ddf950279e5c
Library of Congress authority ID	wds:Q43166481-4FBE3B42-EDD8-4276-9730-FF11EF2134CF
date of birth	wds:Q43166481-C9C3EC88-60B5-48C8-A184-949E6D8EF18B
educated at	wds:Q43166481-0DAF81E8-19CD-4B5B-BE01-F7C518ABFD88 wds:Q43166481-77774B74-8908-4B50-AA99-9D13AE44739F
family name	wds:Q43166481-769574E9-B9CF-488A-971A-09752F1FC9DB
WorldCat Identities ID (superseded)	wds:Q43166481-F1BB1295-B594-4375-B640-086974DA224E
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p382714628
VIAF ID	http://viaf.org/viaf/312881921
GND ID	https://d-nb.info/gnd/13065082X
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2014152772
Nationale Thesaurus voor Auteursnamen ID	382714628
occupation	researcher
employer	Swiss Federal Institute of Technology in Lausanne
NUKAT ID	n2015144094
sex or gender	male
ISNI	0000000444203010
VIAF ID	312881921
GND ID	13065082X
Library of Congress authority ID	no2014152772
date of birth	1977-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Stuttgart
family name	Cramer
WorldCat Identities ID (superseded)	lccn-no2014152772
ORCID iD	wds:Q43166481-64A382F9-24D1-41E5-B96E-68F8B0084978
ORCID iD	https://orcid.org/0000-0001-5740-8494
ORCID iD	0000-0001-5740-8494
is owl:sameAs of	Nicolai Cramer
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q43166481
is author of	Synthesis and biological properties of cylindramide derivatives: evidence for calcium-dependent cytotoxicity of tetramic acid lactams Neutral chiral cyclopentadienyl Ru(ii)Cl catalysts enable enantioselective [2+2]-cycloadditions A tunable class of chiral Cp ligands for enantioselective rhodium(III)-catalyzed C-H allylations of benzamides Chiral Cyclopentadienyls: Enabling Ligands for Asymmetric Rh(III)-Catalyzed C-H Functionalizations Asymmetric Catalysis Powered by Chiral Cyclopentadienyl Ligands. Chiral Cationic Cp(x)Ru(II) Complexes for Enantioselective Yne-Enone Cyclizations. Chiral cyclopentadienyl ligands as stereocontrolling element in asymmetric C-H functionalization. Cyclobutanes in catalysis Chiral monodentate phosphines and bulky carboxylic acids: cooperative effects in palladium-catalyzed enantioselective C(sp3)-H functionalization Concise total synthesis of (+/-)-marcfortine B. Access to β-lactams by enantioselective palladium(0)-catalyzed C(sp3)-H alkylation. Biomimetic synthesis of (+)-ledene, (+)-viridiflorol, (-)-palustrol, (+)-spathulenol, and psiguadial A, C, and D via the platform terpene (+)-bicyclogermacrene Asymmetric synthesis of isoindolones by chiral cyclopentadienyl-rhodium(III)-catalyzed C-H functionalizations. Highly enantioselective rhodium(I)-catalyzed activation of enantiotopic cyclobutanone C-C bonds. Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes Enantioselective palladium-catalyzed direct arylations at ambient temperature: access to indanes with quaternary stereocenters Chiral Cp-rhodium(III)-catalyzed asymmetric hydroarylations of 1,1-disubstituted alkenes. Highly enantioselective rhodium(I)-catalyzed carbonyl carboacylations initiated by C-C bond activation Synthesis of functionalized spiroindolines via palladium-catalyzed methine C-H arylation Palladium(0)-catalyzed enantioselective C-H arylation of cyclopropanes: efficient access to functionalized tetrahydroquinolines Access to sultams by rhodium(III)-catalyzed directed C-H activation Enantioselective synthesis of indanols from tert-cyclobutanols using a rhodium-catalyzed C-C/C-H activation sequence

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