Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Hussein Al-Mughaid"'
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100548- (2022)
In the present study, a facile synthesis of six monovalent α-d-mannoside ligands terminated with phthalimido moiety by Cu(I) catalyzed azide-alkyne cycloaddition reaction (CuAAC) has been achieved. All synthesized ligands were tested for their inhib
Externí odkaz:
https://doaj.org/article/575c0f23e1ce407fafa0656658976e00
Publikováno v:
Carbohydrate Research. 515:108559
Two families (A, B) of triazole conjugates derived from d-mannose possessing reversed linkage functionality were easily assembled by Cu(I) catalyzed azide-alkyne cycloaddition reaction (CuAAC). The mannose precursors were built with either 3-azidopro
Autor:
Maha Khazaaleh, Hussein Al-Mughaid
Publikováno v:
Carbohydrate Research. 508:108396
Six mono-, di-, and trivalent α- d -mannopyranosyl conjugates built on aromatic scaffolds were synthesized in excellent yields by Cu(I) catalyzed azide-alkyne cycloaddition reaction (CuAAC). These conjugates were designed to have unique, flexible ta
Publikováno v:
Carbohydrate Research. :76-84
A series of monovalent α-D-mannoside ligands terminated with aromatic methyl esters have been synthesized in excellent yields using the Cu(I) catalyzed azide-alkyne 1,3-dipolar cycloaddition ("click chemistry"). These mannosides were designed to hav
Publikováno v:
Groundwater for Sustainable Development. 12:100505
Contamination of groundwater resources from nitrates is a worldwide problem, and Jordan is not an exception. Source identification of contamination is a prerequisite for the protection of water resources and human health. Moreover, investigating the
Publikováno v:
Carbohydrate Research. 417:27-33
The synthesis of novel tetrameric and hexameric mannoside clusters bearing 1,2,3-trizole linkages via Cu(I)-catalyzed azide-alkyne cycloaddition reaction ("click chemistry") is described. An attractive feature of these multiarmed mannoside clusters a
Publikováno v:
European Journal of Organic Chemistry. 2015:5501-5508
A facile, efficient, and gram-scale method for the conversion of para-anisic acid into 3,4,5-triiodoanisole through a one-pot C–H iodination/ipso-iododecarboxylation reaction was investigated. Commercially available benzoic acid was used, which all
Autor:
Nawal K. Paul, Tyler Mercer, Hussein Al-Mughaid, T. Bruce Grindley, Michael McAlduff, Kulbir Singh, D. Gerrard Marangoni
Publikováno v:
Canadian Journal of Chemistry. 93:502-508
The surface and self-assembly properties of a family of multiheaded, multitailed surfactants based on a tripentaerythritol backbone are described. Critical aggregation concentrations of these unusual surfactant systems have been determined from surfa
Publikováno v:
ChemInform. 46
A facile, efficient, and gram-scale method for the conversion of para-anisic acid into 3,4,5-triiodoanisole through a one-pot C–H iodination/ipso-iododecarboxylation reaction was investigated. Commercially available benzoic acid was used, which all
Publikováno v:
Tetrahedron. 66:9602-9609
Six dendrimer and dendron cores terminated by hydroxyl groups that are neither phenolic nor cleavable by hydrogenolysis have been prepared in a consistent one-pot manner from terminal allyl groups by reduction of the product of reductive ozonolysis.