Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Eirini Antonatou"'
Autor:
Dimitris Kalaitzakis, Tamsyn Montagnon, Georgios I. Ioannou, Eirini Antonatou, Georgios Vassilikogiannakis
Publikováno v:
ARKIVOC, Vol 2015, Iss 3, Pp 154-166 (2015)
Externí odkaz:
https://doaj.org/article/8b464bdc7a094fd88eacfea0b3b7cbe5
Autor:
Ewout De Geyter, Laure Tack, Emiel Ongenae, Georgios Vassilikogiannakis, Abhishek Iyer, Dimitris Kalaitzakis, Annemieke Madder, Eirini Antonatou, Sabina Smolen
Publikováno v:
CHEMICAL SCIENCE
Chemical Science
Chemical Science
Recent dramatic expansion in potential uses of protein conjugates has fueled the development of a wide range of protein modification methods; however, the desirable single-site multi-functionalization of proteins has remained a particularly intransig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::490a783cb44b59df6365918da9347f36
https://biblio.ugent.be/publication/8714036
https://biblio.ugent.be/publication/8714036
Publikováno v:
Organic & Biomolecular Chemistry. 15:8140-8144
We here describe a furan oxidation based site-specific chemical ligation approach using unprotected peptide segments. This approach involves two steps: after photooxidation of a furan-containing peptide, ligation is achieved by reaction of the unmask
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b52fb5fd5e8ea2e5494cd370a8ced00
https://doi.org/10.1039/c7ob02245j
https://doi.org/10.1039/c7ob02245j
Autor:
Georgios Vassilikogiannakis, Georgios I. Ioannou, Tamsyn Montagnon, Eirini Antonatou, Dimitris Kalaitzakis
Publikováno v:
ARKIVOC, Vol 2015, Iss 3, Pp 154-166 (2015)
Using a sustainable, green and one-pot protocol, simple furans are transformed into complex aromatic nitrogen-bearing polycycles that are synthetically important. The reaction, which is performed in water, begins with the highly selective and mild ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2341501d655463c78d87f122923d8c87
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.973
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.973
Autor:
Eirini Antonatou, Evelien Focquet, Dorien Van Lysebetten, Lieselot L. G. Carrette, Filip Du Prez, Stefania Felissati, Pieter Espeel, Annemieke Madder
Publikováno v:
Chembiochem : a European journal of chemical biology. 19(6)
The development of straightforward and versatile peptide cyclisation methods is highly desired to meet the demand for more stable peptide-based drugs. Herein, a new method for the synthesis of side-chain-to-tail cyclic peptides with the simultaneous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7604d7787da1a41ee9a1886b0ffdc34
https://pubmed.ncbi.nlm.nih.gov/29314620
https://pubmed.ncbi.nlm.nih.gov/29314620
Peptide and protein labelling methods have been under continuous development over the last few decades. Labelled proteins and peptides are undoubtedly indispensable for the study of biological processes at a molecular level. Nowadays, labels can be o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d0e1a318b1a11e0f2eb0dc895af3c88
https://doi.org/10.1039/9781782626619-00053
https://doi.org/10.1039/9781782626619-00053
Autor:
Annemieke Madder, Dimitris Kalaitzakis, Georgios Vassilikogiannakis, Kurt Hoogewijs, Eirini Antonatou, Andreas Baudot
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(25)
A novel chemoselective ligation methodology has been developed for the facile construction of peptide-based fluorescent probes. Furan-containing peptides were activated by singlet oxygen and covalently engaged by nitrogen nucleophiles to yield stable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958f147d81fd205ae49b9394b884062a
https://pubmed.ncbi.nlm.nih.gov/27113264
https://pubmed.ncbi.nlm.nih.gov/27113264
Publikováno v:
ChemInform. 45
A range of 1-azaspirocycles, spiroaminals and 1,6-diazaspirocycles, are synthesized starting from readily accessible furan precursors using a cascade reaction sequence initiated by singlet oxygen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99fee8876ddc317a11119e95cd270852
https://doi.org/10.1002/chin.201419100
https://doi.org/10.1002/chin.201419100
Autor:
Tamsyn Montagnon, Georgios Vassilikogiannakis, Eirini Antonatou, Nuria Bardaji, Dimitris Kalaitzakis
Publikováno v:
ChemInform. 44
A general one-pot reaction sequence is developed to convert simple furan derivatives into nitrogen-bearing polycyclic heterocycles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba736e3ff2c44a78bad663eb4a1afa2
https://doi.org/10.1002/chin.201351176
https://doi.org/10.1002/chin.201351176
Publikováno v:
ChemInform. 44
A new and efficient one-pot four step sequence allows the synthesis of erythrinanes (III) and (IV) from furyl aldehyde (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06c37497a5efa73489d3605111265d4c
https://doi.org/10.1002/chin.201350172
https://doi.org/10.1002/chin.201350172