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Organic Letters|September 26, 2008
Tetrazoles are potent anion recognition elements that emulate the disfavored anti conformations of carboxylic acidsAaron H McKie, Sayuri Friedland, Fraser Hof
Chemical Communications (Cambridge, England)|November 1, 2011
Just add tetrazole: 5-(2-pyrrolo)tetrazoles are simple, highly potent anion recognition elementsRebecca J M Courtemanche, Thomas Pinter, Fraser Hof
The Journal of Organic Chemistry|December 17, 2013
Minimalist synthetic host with stacked guanidinium ions mimics the weakened hydration shells of protein-protein interaction interfacesXing Wang, Joshua Post, Dennis K Hore, et al.
Angewandte Chemie (International Ed. in English)|September 16, 2009
Molecular encapsulationFraser Hof, Stephen L Craig, Colin Nuckolls, et al.
The Journal of Organic Chemistry|April 6, 2011
Recognition properties of carboxylic acid bioisosteres: anion binding by tetrazoles, aryl sulfonamides, and acyl sulfonamides on a calix[4]arene scaffoldThomas Pinter, Subrata Jana, Rebecca J M Courtemanche, et al.
The Analyst|September 3, 2014
Quantification of an exogenous cancer biomarker in urinalysis by Raman spectroscopyGuangyi Cao, Ghazal Hajisalem, Wei Li, et al.
Chemical Communications (Cambridge, England)|January 25, 2006
Anion-pi interaction augments halide binding in solutionOrion B Berryman, Fraser Hof, Michael J Hynes, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|February 22, 2017
Aza-amino acid scanning of chromobox homolog 7 (CBX7) ligandsMariam Traoré, Michael Gignac, Ngoc-Duc Doan, et al.
Journal of the American Chemical Society|March 5, 2004
Kinetically stable complexes in water: the role of hydration and hydrophobicityShannon M Biros, Elke C Ullrich, Fraser Hof, et al.
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