About: James Gardiner

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

industrial chemist, organic chemical synthesis

Attributes	Values
rdf:type	Item
field of work	wds:Q40192643-22770fe5-4d3c-3cfa-90ab-044c4545afa7 wds:Q40192643-3df621e3-4af5-fa1f-f089-2a3637878906
field of work	organic synthesis industrial chemistry
description	scheikundige (nl) հետազոտող (hy) industrial chemist, organic chemical synthesis (en)
exact match	wds:Q40192643-6B08A7DA-440C-46E8-AC7A-061FBED306FC
exact match	https://scigraph.springernature.com/person.01200501325.01
rdfs:label	James Gardiner (en) James Gardiner (es) James Gardiner (nl) James Gardiner (ast) James Gardiner (sl) James Gardiner (sq) James Gardiner (it)
skos:prefLabel	James Gardiner (en) James Gardiner (es) James Gardiner (nl) James Gardiner (ast) James Gardiner (sl) James Gardiner (sq) James Gardiner (it)
name	James Gardiner (en) James Gardiner (es) James Gardiner (nl) James Gardiner (ast) James Gardiner (sl) James Gardiner (sq) James Gardiner (it)
Scopus author ID	wds:Q40192643-94E71C24-570C-4ADE-ACCB-C90F46406F87
Scopus author ID	23077129000
given name	wds:Q40192643-10921CBE-4145-4542-B01E-E30C68499BDF
given name	James
instance of	wds:Q40192643-799F6780-FA48-4FD5-9D59-8FCC7AC6DEDE
described at URL	wds:Q40192643-229cc0cf-408a-a0a2-34f0-20ddafbb1eaa
instance of	Homo sapiens
described at URL	https://people.csiro.au/G/J/James-Gardiner
Loop ID	wds:Q40192643-1797561A-B8C3-44E5-958C-6A8C6761D048
Loop ID	290516
ResearchGate profile ID	wds:Q40192643-c7fb6e42-4175-730c-dc2c-07f5fd8937e1
ResearchGate profile ID	James_Gardiner7
academic thesis	wds:Q40192643-0925BF76-9872-4989-A630-41A0A6087C92 wds:Q40192643-E3C309A7-D33E-4581-B440-6BF24E327619
academic thesis	The Synthesis of Conformationally Restricted Amino Acides and Peptide Mimics Using Ring-Closed Metathesis. Conformationally restricted amino acid analogues based on lactams
Google Scholar author ID	wds:Q40192643-a6061c66-4e5f-9d10-7059-bb81266bf14f
Google Scholar author ID	joeXzwQAAAAJ
occupation	wds:Q40192643-75E77E95-B069-44F3-A11D-5292AA8A1D15
employer	wds:Q40192643-88C72CE9-EA16-4756-A913-4AA5217373CD
sex or gender	wds:Q40192643-9ADADBD6-A40C-4758-971B-5D03939DA941
on focus list of Wikimedia project	wds:Q40192643-9036A09D-E3BD-4351-A53F-D0BF9462ACB6
academic degree	wds:Q40192643-08D81543-331A-4A76-AC98-ED2FA938CFAC wds:Q40192643-C406BFDA-5C27-4E30-88E4-4B923725090E
educated at	wds:Q40192643-5e6b2aae-4e39-990e-7668-0b5b3e33dc92
family name	wds:Q40192643-7E8C5C05-D860-459A-A218-392C389F2B70
occupation	chemist
employer	Commonwealth Scientific and Industrial Research Organisation
sex or gender	male
on focus list of Wikimedia project	NZThesisProject
academic degree	Doctor of Philosophy
educated at	University of Canterbury
family name	Gardiner
ORCID iD	wds:Q40192643-FB00C378-BD29-4CD7-AE37-1E91B3B47636
Dimensions author ID	wds:Q40192643-0B1B475F-0106-47B8-BF61-0A325F51098C
ORCID iD	https://orcid.org/0000-0003-0298-5790
ORCID iD	0000-0003-0298-5790
Dimensions author ID	01200501325.01
ResearcherID	wds:Q40192643-2EADE38A-A071-4B01-B3FB-E97F90E04E67
ResearcherID	D-4774-2011
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q40192643
is author of	Beta-peptidic peptidomimetics Emerging rules for effective antimicrobial coatings Synthesis and biological evaluation of phosphatidylinositol phosphate affinity probes Imaging of a beta-peptide distribution in whole-body mice sections by MALDI mass spectrometry Total Chemical Synthesis of an Intra-A-Chain Cystathionine Human Insulin Analogue with Enhanced Thermal Stability 2-nitroveratryl as a photocleavable thiol-protecting group for directed disulfide bond formation in the chemical synthesis of insulin. Synthesis of cyclic beta-amino acid esters from methionine, allylglycine, and serine Permeation of a beta-heptapeptide derivative across phospholipid bilayers. On the terminal homologation of physiologically active peptides as a means of increasing stability in human serum--neurotensin, opiorphin, B27-KK10 epitope, NPY. Solution Structures of β Peptides from Raman Optical Activity Interaction of alpha-and beta-oligoarginine-acids and amides with anionic lipid vesicles: a mechanistic and thermodynamic study. The enantiomer of octreotate binds to all five somatostatin receptors with almost equal micromolar affinity--a comparison with SANDOSTATIN. Synthesis, structure, and biological applications of α-fluorinated β-amino acids and derivatives New Open-Chain and Cyclic Tetrapeptides, Consisting ofα-,β2-, andβ3-Amino-Acid Residues, as Somatostatin Mimics - A Survey Enzymatic degradation of beta- and mixed alpha,beta-oligopeptides ADME investigations of unnatural peptides: distribution of a 14C-labeled beta 3-octaarginine in rats Comparison of Permeation through Phosphatidylcholine Bilayers ofN-Dipicolinyl-α- and -β-Oligopeptides NMR-Solution Structures of Fluoro-Substitutedβ-Peptides: A314-Helix and a Hairpin Turn. The First Case of a 90° OCCF Dihedral Angle in anα-Fluoro-Amide Group Use of Catalytic Static Mixers for Continuous Flow Gas–Liquid and Transfer Hydrogenations in Organic Synthesis Fluoropolymers: Origin, Production, and Industrial and Commercial Applications A diastereoselective synthesis of the tetrahydropyridazinone core of 2-oxo-1,6-diazobicyclo[4.3.0]nonane-9-carboxylate-based peptidomimetics starting from (S)-phenylalanine Rational design of a hexapeptide hydrogelator for controlled-release drug delivery Controlling self-assembly of diphenylalanine peptides at high pH using heterocyclic capping groups The Synthesis of Conformationally Restricted Amino Acides and Peptide Mimics Using Ring-Closed Metathesis. Analysis of cellular phosphatidylinositol (3,4,5)-trisphosphate levels and distribution using confocal fluorescent microscopy Synthesis and solid state conformation of phenylalanine mimetics constrained in a proline-like conformation Dithiocarbamate RAFT agents with broad applicability – the 3,5-dimethyl-1H-pyrazole-1-carbodithioates β-Aminopeptidase-Catalyzed Biotransformations of β2-Dipeptides: Kinetic Resolution and Enzymatic Coupling

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