About: Paul Lloyd-Williams

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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) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Paul Lloyd-Williams (en) Paul Lloyd-Williams (es) Paul Lloyd-Williams (fr) Paul Lloyd-Williams (it) Paul Lloyd-Williams (nl) Paul Lloyd-Williams (sl) Paul Lloyd-Williams (ast)
skos:prefLabel	Paul Lloyd-Williams (en) Paul Lloyd-Williams (es) Paul Lloyd-Williams (fr) Paul Lloyd-Williams (it) Paul Lloyd-Williams (nl) Paul Lloyd-Williams (sl) Paul Lloyd-Williams (ast)
name	Paul Lloyd-Williams (en) Paul Lloyd-Williams (es) Paul Lloyd-Williams (fr) Paul Lloyd-Williams (it) Paul Lloyd-Williams (nl) Paul Lloyd-Williams (sl) Paul Lloyd-Williams (ast)
given name	wds:Q48358318-8EB927C4-A78F-4788-8717-21A7256273A2
given name	Paul
instance of	wds:Q48358318-09848017-C8EC-4EDC-8C76-A8EB2CCBBE11
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q48358318-dcb0fd4f-2746-4842-982f-f4a101061d4a
occupation	wds:Q48358318-F25D19A3-C780-4114-A8E5-250BB17DD16F
employer	wds:Q48358318-3215728C-B916-4BF5-996E-DE27E977178F
University of Barcelona authority ID	wds:Q48358318-2C099683-5CD0-4216-A207-59BFACE2BFEF
NUKAT ID	wds:Q48358318-7BF9E542-0338-4174-9EC8-D36999B93980
University of Barc...D (former scheme)	wds:Q48358318-B582E30C-94CB-4E40-A065-E7E2A233A54E
sex or gender	wds:Q48358318-B5DB8784-1F28-4619-BD0D-5C9648AC6152
ISNI	wds:Q48358318-686042D3-6F4B-4F3F-A24C-4C9EBACCF55A
VIAF ID	wds:Q48358318-39AA32C3-51BB-4320-B7F9-AB2F26EC58F3
Library of Congress authority ID	wds:Q48358318-D7B4F12A-C671-465F-BC17-9C4EE3A8DDC9
IdRef ID	wds:Q48358318-3D613799-B745-4770-BA98-13BA302EAE2B
WorldCat Identities ID (superseded)	wds:Q48358318-6ADA334F-4DEF-471F-851C-13DEA2BE7B1A
National Library of Israel J9U ID	wds:Q48358318-246CC7F4-A7E8-4F1A-92E1-88A75B4CC1DD
CANTIC ID	wds:Q48358318-38BA6005-9286-45D3-9778-D6D6A025D643
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p194980898
VIAF ID	http://viaf.org/viaf/182754
Library of Congress authority ID	http://id.loc.gov/authorities/names/n97013879
IdRef ID	http://www.idref.fr/053486722/id
Nationale Thesaurus voor Auteursnamen ID	194980898
occupation	researcher
employer	University of Barcelona
University of Barcelona authority ID	981058529876806706
NUKAT ID	n2005130631
University of Barc...D (former scheme)	a1263936
sex or gender	male
ISNI	0000000117357768
VIAF ID	182754
Library of Congress authority ID	n97013879
IdRef ID	053486722
WorldCat Identities ID (superseded)	lccn-n97013879
National Library of Israel J9U ID	987007460113505171
CANTIC ID	981058529876806706
ORCID iD	wds:Q48358318-AB476C9A-BCF1-445B-9F57-33952BDE5527
Dimensions author ID	wds:Q48358318-25114045-9DE8-4FF2-8EAC-027C313572FB
ORCID iD	https://orcid.org/0000-0003-1618-1822
ORCID iD	0000-0003-1618-1822
Dimensions author ID	01003022430.47
ResearcherID	wds:Q48358318-AAB9FA27-341F-470D-8AE4-616407210234
Publons author ID	wds:Q48358318-b09327cd-eacb-4327-899b-73abb8a878c7
ResearcherID	K-4378-2014
Publons author ID	2494323
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q48358318
is author of	Convergent solid-phase peptide synthesis Total Synthesis of Dehydrodidemnin B. Use of Uronium and Phosphonium Salt Coupling Reagents in Peptide Synthesis in Solution† Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides Convergent solid-phase peptide synthesis. XI. Synthesis and purification of protected peptide segments spanning the entire sequence of the uteroglobin monomer using the photolabile nbb-resin Convergent solid-phase peptide synthesis. X. Synthesis and purification of protected peptide fragments using the photolabile Nbb-resin Solid-phase synthesis of peptides using allylic anchoring groups. An investigation of their palladium-catalysed cleavage Use of BOP reagent for the suppression of diketopiperazine formation in boc/bzl solid-phase peptide synthesis Arylboronic acids and arylpinacolboronate esters in Suzuki coupling reactions involving indoles. Partner role swapping and heterocycle protection Severe side-reaction in the acidolytic cleavage of a C-terminal Met-containing peptide from the solid support. Formation of the homoserine lactone peptide Molecules Designed to Contain Two Weakly Coupled Spins with a Photoswitchable Spacer Total synthesis of (-)-isoavenaciolide Analysis of conformational equilibria in aplidine using selective excitation 2D NMR spectroscopy and molecular mechanics/dynamics calculations Racemization in suzuki couplings: a quantitative study using 4-hydroxyphenylglycine and tyrosine derivatives as probe molecules Simple methods for the preparation of protected derivatives of and Synthesis, conformational analysis, and cytotoxicity of conformationally constrained aplidine and tamandarin A analogues incorporating a spirolactam beta-turn mimetic. Use of the SPhos ligand to suppress racemization in arylpinacolboronate ester Suzuki couplings involving alpha-amino acids. Synthesis of biaryl derivatives of 4-hydroxyphenylglycine, tyrosine, and tryptophan A Useful Allene for the Stereoselective Synthesis of Protected Quaternary 2-Amino-2-vinyl-1,3-diols. Designed asymmetric coordination helicates with bis-β-diketonate ligands

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