Zobrazeno 1 - 10
of 497
pro vyhledávání: '"John M Gardiner"'
Publikováno v:
Designed Monomers and Polymers, Vol 26, Iss 1, Pp 117-131 (2023)
The synthesis of glycopolymers by copolymerising an allyl glucosamine (AG) monomer with co-monomers methyl methacrylate (MMA), acrylonitrile (AN) and 2-hydroxyethyl methacrylate (HEMA) was investigated via free-radical polymerisation of 2,2-azobisiso
Externí odkaz:
https://doaj.org/article/ff039db5df1e4da8b44ac78354076db5
Akademický článek
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Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 1, Pp 3571-3584 (2020)
An efficient synthesis of the new (E)-N′-(3,4-dimethoxybenzylidene)furan-2-carbohydrazide is described. Its molecular structural features have been characterized by FTIR, 1H NMR, 13C NMR and MS, then have been confirmed by single crystal X-ray diff
Externí odkaz:
https://doaj.org/article/cc0b2c499bde433f8504cb282589439a
Autor:
Fahad Ayesh Alharthi, Garrett T. Potter, Gordon C. Jayson, George F. S. Whitehead, Iñigo J. Vitórica-Yrezábal, John M. Gardiner
Publikováno v:
Organic Letters. 25:2196-2200
Autor:
Rami Y. Morjan, Said M. El-Kurdi, Jannat N. Azarah, Neda A. Eleiwa, Omar S. Abu-Teim, Adel M. Awadallah, James Raftery, John M. Gardiner
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 9, Pp 1362-1365 (2018)
Trimethyl citrate, C9H14O7 (systematic name: trimethyl 2-hydroxypropane-1,2,3-tricarboxylate), 2, was prepared by the esterification of citric acid and methanol in the presence of thionyl chloride at 273 K. The bond lengths and angles in 2 compare cl
Externí odkaz:
https://doaj.org/article/35880002a57d45478dfb347045f5d885
Autor:
Rami Y. Morjan, Amany F. El-Hallaq, Jannat N. Azarah, Ihab M. Almasri, Mazen M. Alzaharna, Mariam R. Al-Reefi, Ian Beadham, Omar S. Abu-Teim, Abdelraouf A. Elmanama, Adel M. Awadallah, James Raftery, John M. Gardiner
Publikováno v:
Journal of Molecular Structure. 1288:135754
Autor:
Marek Baráth, Steen U. Hansen, Charlotte E. Dalton, Gordon C. Jayson, Gavin J. Miller, John M. Gardiner
Publikováno v:
Molecules, Vol 20, Iss 4, Pp 6167-6180 (2015)
Heparin and heparan sulphate (H/HS) are important members of the glycosaminoglycan family of sugars that regulate a substantial number of biological processes. Such biological promiscuity is underpinned by hetereogeneity in their molecular structure.
Externí odkaz:
https://doaj.org/article/1e16d2015b644657a226a97d08326947
Autor:
John M. Gardiner, James Raftery, Ian G. Beadham, Jannat N. Azarah, Mohammed Y. Abu-Foul, Adel M. Awadallah, Rami Y. Morjan
Publikováno v:
Zeitschrift für Kristallographie - New Crystal Structures. 238:109-110
C8H10N2O2, orthorhombic, Pbca (no. 61), a = 11.0571(2) Å, b = 8.1172(2) Å, c = 17.6080(4) Å, V = 1580.37(6) Å3, Z = 8, R gt (F) = 0.0324, wR ref (F 2) = 0.0872, T = 100(2) K.
Publikováno v:
Carbohydrate Research. 524:108744
Autor:
Egle Avizienyte, Claire L Cole, Graham Rushton, Gavin J Miller, Antonella Bugatti, Marco Presta, John M Gardiner, Gordon C Jayson
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0159739 (2016)
Heparan sulphate (HS), a ubiquitously expressed glycosaminoglycan (GAG), regulates multiple cellular functions by mediating interactions between numerous growth factors and their cell surface cognate receptors. However, the structural specificity of
Externí odkaz:
https://doaj.org/article/44a851b5c5644841994c9c35f621831b