
{"id":19,"date":"2012-11-20T19:31:37","date_gmt":"2012-11-20T19:31:37","guid":{"rendered":"http:\/\/pages.charlotte.edu\/john-risley\/?page_id=19"},"modified":"2013-04-08T18:45:42","modified_gmt":"2013-04-08T18:45:42","slug":"publications","status":"publish","type":"page","link":"http:\/\/pages.charlotte.edu\/john-risley\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<ol start=\"24\">\n<li>J. M. Risley and R. L. Van Etten (1990) &#8220;Assignment of Oligosaccharide Structures to Specific Sites on Human Prostatic Acid Phosphatase&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Protein Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">9<\/span>, 366-367.<\/li>\n<li>J. M. Risley (1991) &#8220;Investigations Utilizing the\u00a0<sup>18<\/sup>O Isotope Shift in\u00a0<sup>13<\/sup>C Nuclear Magnetic Resonance Spectroscopy.\u00a0 1.\u00a0 Correlation with\u00a0<sup>17<\/sup>O NMR Chemical Shifts&#8221;\u00a0<span style=\"text-decoration: underline;\">Magn. Reson. Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">29<\/span>, 143-147.<\/li>\n<li>W. Arias and J. M. Risley (1991) &#8220;Investigations Utilizing the\u00a0<sup>18<\/sup>O Isotope Shift in\u00a0<sup>13<\/sup>C Nuclear Magnetic Resonance Spectroscopy.\u00a0 2.\u00a0 Observation of a Downfield Isotope Shift in 2,6-Dimethyl-4-pyrone&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Org. Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">56<\/span>, 3741-3744.<\/li>\n<li>J. M. Risley (1991) &#8220;Preparing Solutions in the Biochemistry Lab.\u00a0 An Essential, Basic Skill&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Chem. Educ.<\/span>\u00a0<span style=\"text-decoration: underline;\">68<\/span>, 1054-1055.<\/li>\n<li>J. R. Rasmussen, J. Davis, J. M. Risley, and R. L. Van Etten (1992) &#8220;Identification and Derivatization of (Oligosaccharyl)amines Obtained by Treatment of Asparagine-Linked Glycopeptides with N-GLYCANASE Enzyme&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Am. Chem. Soc.<\/span>\u00a0<span style=\"text-decoration: underline;\">114<\/span>, 1124-1126.<\/li>\n<li>J. M. Risley (1996) &#8220;An Organoleptic Laboratory Experiment&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Chem. Educ.<\/span>\u00a0<span style=\"text-decoration: underline;\">73<\/span>, 1181-1183.<\/li>\n<li>L. J. Hasbrouck, C.M. Carlin, and J. M. Risley (1997) &#8220;Origin of the oxygen in the oxidation of triphenylphosphine by potassium perphosphate&#8221;\u00a0<span style=\"text-decoration: underline;\">Inorg. Chim. Acta<\/span>\u00a0<span style=\"text-decoration: underline;\">258<\/span>, 123-125.<\/li>\n<li>L. J. Hasbrouck and J. M. Risley (1998) &#8220;Investigations Utilizing the\u00a0<sup>18<\/sup>O Isotope Shift in\u00a0<sup>13<\/sup>C Nuclear Magnetic Resonance Spectroscopy. 3. Observation of a Solvent Dependence for tert-Butyl Alcohol&#8221;\u00a0<span style=\"text-decoration: underline;\">Tetrahedron Lett.<\/span>\u00a0<span style=\"text-decoration: underline;\">39<\/span>, 4191-4194.<\/li>\n<li>D. H. Huang and J. M. Risley (2000) &#8220;Synthesis of N<sup>4<\/sup>-(2-acetamido-2-deoxy-b-D-glucopyranosyl)-L-asparagine analogues:\u00a0 Succinamide, L-2-hydroxysuccinamide, and L-2-hydroxysuccinamic acid hydrazide analogues&#8221;\u00a0<span style=\"text-decoration: underline;\">Carbohydr. Res.<\/span>\u00a0<span style=\"text-decoration: underline;\">329<\/span>, 487-493.<\/li>\n<li>32a.\u00a0D. H. Huang and J. M. Risley (2001) Corrigendum to \u201cSynthesis of N<sup>4<\/sup>-(2-acetamido-2-deoxy-b-D-glucopyranosyl)-L-asparagine analogues:\u00a0 Succinamide, L-2-hydroxysuccinamide, and L-2 hydroxysuccinamic acid hydrazide analogues\u201d\u00a0<span style=\"text-decoration: underline;\">Carbohydr.<\/span><span style=\"text-decoration: underline;\">Res.<\/span>\u00a0<span style=\"text-decoration: underline;\">331,<\/span>\u00a0225.<\/li>\n<li>Y.-Q. Xia and J. M. Risley (2001) &#8220;Synthesis of N<sup>4<\/sup>-(2-Acetamido-2-deoxy-b-D-glucopyranosyl)-L-Asparagine Analogues. L-2-Chloro-, L-2-Bromo-, and D,L-2-Methylsuccinamic Acid Analogues&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Carbohydr. Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">20<\/span>, 45-55.<\/li>\n<li>J. J. Malik and J. M. Risley (2001) &#8220;Synthesis of N<sup>4<\/sup>-(2-acetamido-2-deoxy-b-D-glucopyranosyl)-L-asparagine analogues.\u00a0 Complete NMR assignments of chloroacetamide, bromoacetamide and glycinamide analogues&#8221;\u00a0<span style=\"text-decoration: underline;\">Magn. Reson. Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">39<\/span>, 98-100.\u00a0 DOI: 10.1002\/1097-458X(200102)39:2&lt;101::AID-MRC797&gt;3.0.CO;2-F<\/li>\n<li>J. J. Kaylor and J. M. Risley (2001) &#8220;Synthesis of N<sup>4<\/sup>-(2-acetamido-2-deoxy-b-D-glucopyranosyl)-L-asparagine analogues:\u00a0 n-Butyramide, 3-chloropropionamide, 3-aminopropionamide, and isovaleramide analogues&#8221;\u00a0<span style=\"text-decoration: underline;\">Carbohydr. Res.<\/span>\u00a0<span style=\"text-decoration: underline;\">331<\/span>, 439-444.<\/li>\n<li>J. M. Risley, D. H. Huang, J. J. Kaylor, J. J. Malik, and Y.-Q. Xia (2001) &#8220;Glycosylasparaginase Inhibition Studies:\u00a0 Competitive Inhibitors, Transition State Mimics, Noncompetitive Inhibitors&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Enzyme Inhib.<\/span>\u00a0<span style=\"text-decoration: underline;\">16<\/span>, 269-274.<\/li>\n<li>J. M. Risley, D. H. Huang, J. J. Kaylor, J. J. Malik, Y.-Q. Xia, and W. M. York (2001) &#8220;Glycosylasparaginase Activity Requires the\u00a0a-Carboxyl Group, But Not the\u00a0a-Amino Group, on N<sup>4<\/sup>-(2-Acetamido-2-Deoxy-b-D-Glucopyranosyl)-L-Asparagine&#8221;<span style=\"text-decoration: underline;\">Arch. Biochem. Biophys.<\/span>\u00a0<span style=\"text-decoration: underline;\">391<\/span>, 165-170.\u00a0 DOI: 10.1006\/abbi.2001.2416<\/li>\n<li>J. M. Risley (2002) &#8220;Cholesterol Biosynthesis:\u00a0 Lanosterol to Cholesterol&#8221;\u00a0<span style=\"text-decoration: underline;\">J. Chem. Educ.<\/span>\u00a0<span style=\"text-decoration: underline;\">79<\/span>, 377-384.<\/li>\n<li>W. Du and J. M. Risley (2003) \u201cAcylation is rate-limiting in glycosylasparaginase-catalyzed hydrolysis of\u00a0<em>N<\/em><sup>4<\/sup>-(4\u00b4-substituted phenyl)-L-asparagines\u201d\u00a0<span style=\"text-decoration: underline;\">Org. Biomol. Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">1<\/span>,\u00a0<span style=\"text-decoration: underline;\">1900-1905.\u00a0 DOI: 10.1039\/b301513k<\/span><\/li>\n<li>J. M. Risley (2007) \u201cReworking Exams To Teach Chemistry Content and Reinforce Student Learning\u201d\u00a0<span style=\"text-decoration: underline;\">J. Chem. Educ.<\/span>\u00a0<span style=\"text-decoration: underline;\">84<\/span>, 1445-1447.<\/li>\n<li>J. M. Risley (2007) \u201cStructures for the ABO(H) Blood Group: Which Textbook is Correct?\u201d\u00a0<span style=\"text-decoration: underline;\">J. Chem. Educ.<\/span>\u00a0<span style=\"text-decoration: underline;\">84<\/span>, 1546-1547.<\/li>\n<li>J. M. Risley, J. P. Kastanis, and A. M. Young (2011) \u201cDetermination of the Second-Order\u00a0<sup>1<\/sup>H NMR Parameters for the Aromatic Protons in 4-Fluoroaniline and Application to the Analysis of the\u00a0<sup>1<\/sup>H NMR Spectra for the Aromatic Protons in\u00a0<em>N<\/em><sup>4<\/sup>-(4\u2032-Fluorophenyl)succinamic Acid and in\u00a0<em>N<\/em><sup>4<\/sup>-(4\u2032-Fluorophenyl-3,3-difluorosuccinamic Acid\u201d\u00a0<span style=\"text-decoration: underline;\">J. Fluorine Chem.<\/span>\u00a0<span style=\"text-decoration: underline;\">132<\/span>, 269-275.\u00a0 DOI: 10.1016\/j.jfluchem.2011.02.003&nbsp;<\/li>\n<li>L. E. Burnham, K. J. Gano, A. M. Young, J. M. Risley, and D. S. Jones (2012) \u201c<em>N<\/em>-(4-Isocyanophenyl)succinamic acid\u201d\u00a0<span style=\"text-decoration: underline;\">Acta Cryst.<\/span>\u00a0<span style=\"text-decoration: underline;\">E68<\/span>, o2078.\u00a0 DOI: 10.1107\/S1600536812025226<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>J. M. Risley and R. L. Van Etten (1990) &#8220;Assignment of Oligosaccharide Structures to Specific Sites on Human Prostatic Acid Phosphatase&#8221;\u00a0J. Protein Chem.\u00a09, 366-367. J. M. Risley (1991) &#8220;Investigations Utilizing the\u00a018O Isotope Shift in\u00a013C Nuclear Magnetic Resonance Spectroscopy.\u00a0 1.\u00a0 Correlation with\u00a017O NMR Chemical Shifts&#8221;\u00a0Magn. Reson. Chem.\u00a029, 143-147. W. Arias and J. M. Risley (1991) &#8220;Investigations [&hellip;]<\/p>\n","protected":false},"author":582,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"jetpack_post_was_ever_published":false,"footnotes":""},"class_list":["post-19","page","type-page","status-publish","hentry"],"jetpack_shortlink":"https:\/\/wp.me\/P2UMQA-j","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/pages\/19","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/users\/582"}],"replies":[{"embeddable":true,"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/comments?post=19"}],"version-history":[{"count":4,"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/pages\/19\/revisions"}],"predecessor-version":[{"id":35,"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/pages\/19\/revisions\/35"}],"wp:attachment":[{"href":"http:\/\/pages.charlotte.edu\/john-risley\/wp-json\/wp\/v2\/media?parent=19"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}