Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Susan E Matthews"'
Autor:
Jean-Jacques Helesbeux, Laura Carro, Florence O. McCarthy, Vânia M. Moreira, Francesca Giuntini, Niamh O’Boyle, Susan E. Matthews, Gülşah Bayraktar, Samuel Bertrand, Christophe Rochais, Pascal Marchand
Publikováno v:
Pharmaceuticals, Vol 14, Iss 12, p 1278 (2021)
The 29th Annual GP2A (Group for the Promotion of Pharmaceutical chemistry in Academia) Conference was a virtual event this year due to the COVID-19 pandemic and spanned three days from Wednesday 25 to Friday 27 August 2021. The meeting brought togeth
Externí odkaz:
https://doaj.org/article/186f3eb6d769421e89d8c8a6c442f19c
Autor:
Samuel BERTRAND, Francesca Giuntini, Vânia Moreira, Niamh O'Boyle, Pascal Marchand, Florence McCarthy, Susan E Matthews, Laura Carro, Christophe Rochais, Jean-Jacques HELESBEUX, Eavan McLoughlin, Gülşah Bayraktar
Publikováno v:
Pharmaceuticals
Pharmaceuticals, Vol 14, Iss 1278, p 1278 (2021)
Pharmaceuticals, Vol 14, Iss 1278, p 1278 (2021)
The 29th Annual GP2A (Group for the Promotion of Pharmaceutical chemistry in Academia) Conference was a virtual event this year due to the COVID-19 pandemic and spanned three days from Wednesday 25 to Friday 27 August 2021. The meeting brought togeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba269fe8f3b0b7a536c0afc5af6f2c8
https://ueaeprints.uea.ac.uk/id/eprint/82764/
https://ueaeprints.uea.ac.uk/id/eprint/82764/
Publikováno v:
Pharmaceuticals, Vol 10, Iss 4, p 97 (2017)
The 25th Conference of GP2A was held on 31 August and 1 September 2017 in Liverpool, UK, with the aim of exchange of ideas and experience, particularly amongst young medicinal chemists. Topics included bioactive compounds from plants and lichens, and
Externí odkaz:
https://doaj.org/article/672656907185416bb3adf8e334227ce3
Autor:
Igor S. Antipin, Ildar Kh. Rizvanov, Susan E. Matthews, Farida B. Galieva, Olga B. Bazanova, A. A. Murav’ev, Kamil A. Ivshin, S. E. Solovieva, Olga Kataeva
Late stage diversification of calix[4]arenes and thiacalix[4]arenes with heterocycles remains a significant synthetic challenge and hampers further exploitation of the scaffolds. Here we describe the development of a short and facile synthetic route
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad48b4d1ef26db256a0875046bac5685
https://ueaeprints.uea.ac.uk/id/eprint/68489/
https://ueaeprints.uea.ac.uk/id/eprint/68489/
Autor:
Garth A. Jones, John E. O'Brien, Samy Cecioni, Colin J. Macdonald, Susan E. Matthews, Stephen H. Ashworth, Sébastien Vidal, David L. Hughes
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (17), pp.4436-4444. ⟨10.1002/chem.201705955⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (17), pp.4436-4444. ⟨10.1002/chem.201705955⟩
International audience; Calix[4]arenes are unique macrocycles that through judicious functionalisation at the lower rim can be either fixed in one of four conformations or remain conformationally flexible. Introduction of propynyl or propenyl groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cf74b893cbcb1e08b6397c5e4e86cac
https://hal-udl.archives-ouvertes.fr/hal-02121302
https://hal-udl.archives-ouvertes.fr/hal-02121302
Autor:
Phatsawee Jansook, Sergey V. Kurkov, Vitaly I. Kalchenko, Elena V. Ukhatskaya, Thorsteinn Loftsson, Roman V. Rodik, Susan E. Matthews
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 79:473-483
The self-aggregation ability of three amphiphilic cationic calix[4]arenes possessing four quaternary amino groups (aminoCAs) was investigated using a variety of methods. All of the studied compounds possess high aggregation ability. Their critical ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4365dd4c219f190cb0f62b7dd44f748b
https://doi.org/10.1007/s10847-013-0370-6
https://doi.org/10.1007/s10847-013-0370-6
Publikováno v:
Journal of Pharmaceutical Sciences. 102:3485-3512
Calix[n]arenes (CAs) are supramolecular compounds able to form guest-host inclusion complexes with metal ions, small organic molecules, and small moieties of larger molecules. Although the CA literature is extensive, relatively few publications deal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb98f84b1fde00d70be63ea2747c2b9
https://doi.org/10.1002/jps.23681
https://doi.org/10.1002/jps.23681
Autor:
Jonathan A. Kitchen, Thomas McCabe, Thorfinnur Gunnlaugsson, Susan E. Matthews, Christophe Lincheneau, Eoin Quinlan
Publikováno v:
Supramolecular Chemistry. 25:869-880
The synthesis and the photophysical studies of a new generation of time resolved luminescent systems based on calix[4]arenes alkylated at the lower rim, capable of hosting lanthanide (III) ions such as terbium and sensitising its emission, are descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2ae64e0012a3752b4307bba75c10b77
https://doi.org/10.1080/10610278.2013.810339
https://doi.org/10.1080/10610278.2013.810339
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 79:47-55
Ionized calixarene derivatives often possess properties of typical surfactants, aggregating in aqueous solutions. Their solubilizing properties, in this case, are often greater than conventional excipients, cyclodextrins. This in addition to their re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6f1e62c5c035cd77d8dc6dac0a93fcc
https://doi.org/10.1007/s10847-013-0302-5
https://doi.org/10.1007/s10847-013-0302-5
Publikováno v:
Organicbiomolecular chemistry. 14(43)
A new family of multivalent ligand platforms, the open-resorcinarenes, has been prepared in a straightforward two-step reaction. Modification of the core gives a range of topologically diverse scaffolds; functionalisation confirms the versatility of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336217654d9cf23baf85ccd1946cfbf6
https://pubmed.ncbi.nlm.nih.gov/27735006
https://pubmed.ncbi.nlm.nih.gov/27735006