Dominea C. K. Rathwell

ORCID: 0000-0001-7809-6565
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About
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Research Areas
  • Synthesis of Indole Derivatives
  • Carbohydrate Chemistry and Synthesis
  • Oxidative Organic Chemistry Reactions
  • Marine Toxins and Detection Methods
  • Bioactive Compounds and Antitumor Agents
  • Glycosylation and Glycoproteins Research
  • Pneumonia and Respiratory Infections
  • Synthetic Organic Chemistry Methods
  • Organic Electronics and Photovoltaics
  • Marine Sponges and Natural Products
  • Microbial Natural Products and Biosynthesis
  • Organic Light-Emitting Diodes Research
  • Respiratory viral infections research
  • Galectins and Cancer Biology
  • Crystallization and Solubility Studies
  • Immunotherapy and Immune Responses
  • Synthesis and Biological Activity
  • Legume Nitrogen Fixing Symbiosis
  • Conducting polymers and applications
  • Polyamine Metabolism and Applications
  • Synthesis and biological activity
  • X-ray Diffraction in Crystallography
  • Luminescence and Fluorescent Materials
  • Synthesis of Organic Compounds
  • Synthesis and Biological Evaluation

Seoul National University of Science and Technology
2019

Max Planck Institute of Colloids and Interfaces
2014-2018

Freie Universität Berlin
2015-2017

Yonsei University
2015

University of Auckland
2008-2012

Maurice Wilkins Centre
2010

Fully synthetic glycan-based vaccines hold great potential as preventive and therapeutic against infectious diseases well cancer. Here, we present a two-component platform based on the facile conjugation of carbohydrate antigens to α-galactosylceramide (α-GalCer) yield fully vaccine candidates. Formulation cancer-associated Tn antigen glycolipid model candidate into liposomes different sizes subsequent immunization mice generated specific, high-affinity antibodies with characteristics T...

10.1021/acs.jmedchem.8b00312 article EN Journal of Medicinal Chemistry 2018-05-09

Balancing act: The correct balance of electronic factors in the naphthazarin and isocoumarin fragments facilitates acid-mediated spiroketalization step to afford key densely functionalized spiroketal (see picture; EOM=ethoxymethyl) formal synthesis (±)-γ-rubromycin. A novel regioselective allyloxylation/Claisen rearrangement 2-azido-1,4-naphthoquinone provides access highly oxygenated fragment. Detailed facts importance specialist readers are published as "Supporting Information". Such...

10.1002/anie.200903316 article EN Angewandte Chemie International Edition 2009-07-30

Dual-modal fluorescent magnetic glyconanoparticles have been prepared and shown to be powerful in probing lectins displayed on pathogenic mammalian cell surfaces. Blood group H1- Leb-conjugated nanoparticles were found bind BabA displaying Helicobacter pylori, Lea- Leb-modified are both recognized by internalized into DC-SIGN SIGN-R1 expressing cells via lectin-mediated endocytosis. In addition, block adhesion of H. pylori cells, suggesting that they can serve as inhibitors infection host...

10.1021/jacs.5b00592 article EN Journal of the American Chemical Society 2015-05-05

A<italic>Haemophilus influenzae</italic>b vaccine lead antigen was identified by the immunological evaluation of chemically precisely defined capsular polysaccharide repeating unit oligosaccharides.

10.1039/c7sc04521b article EN cc-by Chemical Science 2017-12-11

Studies toward the synthesis of three biologically active [5,6]-benzannulated spiroketal natural products are described. The first total paecilospirone is reported, employing a late-stage, pH-neutral spiroketalization. A formal γ-rubromycin described, where moiety formed by delicate manipulation electronic properties spirocyclization precursor. Finally, model work berkelic acid summarized, introducing novel Horner–Wadsworth–Emmons/oxa-Michael (HWE/oxa-M) cascade to access

10.1351/pac-con-11-08-06 article EN Pure and Applied Chemistry 2011-10-31

Host-guest structures are used in most state-of-the-art organic light-emitting devices, with the host transporting charge and confining excitons on guest. While often plays a critical role achieving high efficiency stability, predicting understanding these effects is persistent design challenge which slows discovery of new active materials. Closely related molecules, differ only by several functional groups, show drastically different degradation behavior. Here, we explore this observation...

10.1063/1.5124802 article EN Applied Physics Letters 2020-02-10

The synthesis of a series 5,5-, 5,6-, and 6,6-mono­benzannulated spiroketals using novel cross-metathesis-radical-­cyclisation approach is reported. Cross metathesis between two olefin coupling partners resulted in the formation heterodimer which upon hydrogenation furnished saturated alcohol product. Oxidative radical cyclisation then afforded desired monobenz­annulated good overall yield.

10.1055/s-0028-1087942 article EN Synlett 2009-02-24

Abstract We demonstrate improved stability in phosphorescent organic light‐emitting devices (OLEDs) by incorporating a wide energy gap host material into an ambipolar emissive layer. Unlike conventional mixed‐host OLEDs that combine hole‐ and electron‐transporting hosts, charge transport this device occurs primarily along the emitter, while serves to modify injection characteristics of This approach allows both width position exciton recombination zone be tuned without introducing exciplex...

10.1002/jsid.761 article EN Journal of the Society for Information Display 2019-03-21

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.200931101 article EN ChemInform 2009-07-09

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.200941141 article EN ChemInform 2009-09-17

In the crystal structure of title compound, C(16)H(16)O(6), a pair naphthoquinone rings are linked via O-H⋯O-C hydrogen bonds in nearly orthogonal arrangement. This dimeric unit is to neighbouring dimer by π-π stacking inter-actions between rings, where distance mean plane naphtoquinone backbones 3.468 Å, and bonds.

10.1107/s1600536808028432 article EN cc-by Acta Crystallographica Section E Structure Reports Online 2008-09-12
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