About: William P. Unsworth

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

British chemist

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) British chemist (en) Suurbritannia keemik (et) chimist britanic (ro) químico británico (es) כימאי בריטי (he) chimiste britannique (fr) químic britànic (ca) químico británico (gl) كيميائي بريطاني (ar) հետազոտող (hy) hulumtues (sq)
rdfs:label	William P Unsworth (nl) William P Unsworth (sl) William P. Unsworth (en) William P. Unsworth (es) William P. Unsworth (tr)
skos:prefLabel	William P Unsworth (nl) William P Unsworth (sl) William P. Unsworth (en) William P. Unsworth (es) William P. Unsworth (tr)
name	William P Unsworth (nl) William P Unsworth (sl) William P. Unsworth (en) William P. Unsworth (es) William P. Unsworth (tr)
Scopus author ID	wds:Q39185278-3E11B636-17D1-4CB9-B4EA-C3F4D28C0041
Scopus author ID	36942678800
given name	wds:Q39185278-70BF7496-4329-4419-B234-6CED2973B629
given name	William
instance of	wds:Q39185278-4740D9A4-F763-44FF-870F-90EDB3C9E534
instance of	Homo sapiens
award received	wds:Q39185278-639d90e3-40a4-a0be-8a80-ba7c93ee1db0
award received	Hickinbottom Award
doctoral student	wds:Q39185278-566D2A22-7422-4A42-8DC2-699CE720331C wds:Q39185278-6C839DAC-BB39-4835-AFD7-3C827755B403 wds:Q39185278-8E9CFEB8-D2AD-4601-BBBD-CE707CE20EAD wds:Q39185278-E5CA54B6-CF54-4FE1-BF9E-E767474A98DB
doctoral student	James Rossi-Ashton Ryan Gordon Epton Tom Stephens Kleopas Palate
ResearchGate profile ID	wds:Q39185278-7a6829ff-47f9-c506-d3d4-0327e768f1bb
ResearchGate profile ID	William-Unsworth
Google Scholar author ID	wds:Q39185278-0545f089-4aa3-a56e-ff37-18b65c90534d
Google Scholar author ID	A7Hp878AAAAJ
skos:altLabel	William Unsworth (en)
occupation	wds:Q39185278-8BB648F5-82EC-43BD-BEDA-F36BB2881CD5 wds:Q39185278-B7C43805-8736-4281-8615-EBFED52CB73F
employer	wds:Q39185278-8C4BB616-711E-426D-A7A7-116FA25FE1D9
work period (start)	wds:Q39185278-B2CFEAFF-B649-4AE6-941B-CBA5EAA7F512
sex or gender	wds:Q39185278-A7E062F4-1D8C-4297-BD71-73F880777D6C
on focus list of Wikimedia project	wds:Q39185278-4CBC6C81-4415-4755-81FA-EFD08331A877
academic degree	wds:Q39185278-E2924122-09C8-4EAF-9E40-ABE880E4921C
educated at	wds:Q39185278-3D45F530-B5D5-4818-BDB6-7145D77294EC
family name	wds:Q39185278-B6311F6E-FE7F-4724-BA12-639625A5CDF6
occupation	senior lecturer researcher
employer	University of York
work period (start)	2008-01-01 00:00:00Z (xsd:dateTime)
sex or gender	male
on focus list of Wikimedia project	UniversityofYorkThesisProject
academic degree	Doctor of Philosophy
educated at	University of Oxford
family name	Unsworth
ORCID iD	wds:Q39185278-F1587BEB-CB76-401A-BB13-2C8566B334A6
ORCID iD	https://orcid.org/0000-0002-9169-5156
ORCID iD	0000-0002-9169-5156
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q39185278
is pr:P3452 of	wdref:5ff0f3abdf345ae6b55f7634b6c99ef57eeb997a
is author of	Ring-Expansion Approach to Medium-Sized Lactams and Analysis of Their Medicinal Lead-Like Properties Direct imine acylation: synthesis of the proposed structures of 'upenamide. From Heteroaromatic Acids and Imines to Azaspirocycles: Stereoselective Synthesis and 3D Shape Analysis Synthesis of Cyclic Peptide Mimetics by the Successive Ring Expansion of Lactams. Iterative Assembly of Macrocyclic Lactones using Successive Ring Expansion Reactions Synthesis of Spirocyclic Indolenines. Selective Synthesis of Six Products from a Single Indolyl α-Diazocarbonyl Precursor. 'Upenamide: trials and tribulations. Stereospecificity in the Au-catalysed cyclisation of monoallylic diols. Synthesis of (+)-isoaltholactone Ring-Expansion Reactions in the Synthesis of Macrocycles and Medium-Sized Rings Internal Nucleophilic Catalyst Mediated Cyclisation/Ring Expansion Cascades for the Synthesis of Medium-Sized Lactones and Lactams Direct Imine Acylation: Rapid Access to Diverse Heterocyclic Scaffolds An expedient protecting-group-free total synthesis of (±)-dievodiamine. Total synthesis of spirobacillene A The Cope rearrangement of gem-dimethyl substituted divinylcyclopropanes Silver(I)- or copper(II)-mediated dearomatization of aromatic ynones: direct access to spirocyclic scaffolds. Preparation and Reactions of Indoleninyl Halides: Scaffolds for the Synthesis of Spirocyclic Indole Derivatives Modular Synthesis of Polycyclic Alkaloid Scaffolds via an Enantioselective Dearomative Cascade

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