{"id":40,"date":"2016-07-25T00:44:53","date_gmt":"2016-07-25T00:44:53","guid":{"rendered":"https:\/\/kroutlab.wordpress.com\/?page_id=40"},"modified":"2023-06-29T13:05:09","modified_gmt":"2023-06-29T17:05:09","slug":"publications","status":"publish","type":"page","link":"https:\/\/krout.scholar.bucknell.edu\/?page_id=40","title":{"rendered":"research publications"},"content":{"rendered":"\n<p><strong>Peer-Reviewed Publications<\/strong> <em>(* indicates undergraduate authors) \u2003 <span style=\"font-size: 85%;\"><a style=\"color: #990099;\" href=\"http:\/\/krout.scholar.bucknell.edu\/publications-no_abstracts\/\">[view non-graphical list]<\/a><\/span><\/em><br><!-- This is a comment: Add ORCid to this page --><\/p>\n<ol>\n<li class=\"publications\" value=\"16\">&#8220;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0021979723005118\" target=\"_blank\" rel=\"noopener noreferrer\">Determining sequential micellization steps of bile salts with multi-CMC modeling<\/a>,&#8221; Rovnyak, D.; He, J.*; Kong, S.*; Eckenroad, K. W.*; Manley, G. A.*; Geffert, R. M.*; Krout, M. R.; Strein, T. G. <em>J. Colloid Interface Sci.<\/em><b> 2023<\/b>, <em>644<\/em>, 496-508; DOI: 10.1016\/j.jcis.2023.03.146. [<a href=\"http:\/\/krout.scholar.bucknell.edu\/files\/2023\/06\/jcis2023_496_si.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supplemental information<\/a>]<br><br>\n<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0021979723005118\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" title=\"multi CMC modeling of DCA\" src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0021979723005118-ga1.jpg\"><\/a><\/li>\n<li class=\"publications\" value=\"15\">&#8220;<a href=\"https:\/\/www.nature.com\/articles\/s41586-022-04480-z\" target=\"_blank\" rel=\"noopener noreferrer\">Human gut bacteria produce \u03a4\u039717-modulating bile acid metabolites<\/a>,&#8221; Paik, D.; Yao, L.; Zhang, Y.; Bae, S.; D&#8217;Agostino, G. D.; Zhang, M.; Kim, E.; Franzosa, E. A.; Avila-Pacheco, J.; Bisanz, J. E.; Rakowski, C. R.*; Vlamakis, H.; Xavier, R. J.; Turnbaugh, P. J.; Longman, R. S.; Krout, M. R.; Clish, C. B.; Rastinejad, F.; Huttenhower, C.; Huh, J. R.; Devlin, A. S. <em>Nature<\/em><b> 2022<\/b>, <em>603<\/em>, 907\u2013912; DOI: 10.1038\/s41586-022-04480-z. [<a href=\"https:\/\/static-content.springer.com\/esm\/art%3A10.1038%2Fs41586-022-04480-z\/MediaObjects\/41586_2022_4480_MOESM1_ESM.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<br><br>\n<a href=\"https:\/\/www.biorxiv.org\/content\/10.1101\/2021.01.08.425913v1\">Preprint<\/a> uploaded to <em>Biorxiv<\/em> on January 9, 2021.<br><a href=\"https:\/\/www.nature.com\/articles\/s41586-022-04480-z\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" title=\"Bile acid metabolites control Tcells\" src=\"http:\/\/krout.scholar.bucknell.edu\/files\/2022\/12\/Nature2022-Fig1-e1669904598848.jpeg\"><\/a><\/li>\n<li class=\"publications\" value=\"14\">&#8220;<a href=\"https:\/\/www.nature.com\/articles\/s41586-019-1785-z\" target=\"_blank\" rel=\"noopener noreferrer\">Bile acid metabolites control Th17 and Treg cell differentiation<\/a>,&#8221; Hang, S.; Paik, D.; Yao, L.; Kim, E.; Jamma, T.; Lu, J.; Ha, S.; Nelson, B. N.; Kelly, S. P.*; Wu, L.; Zheng, Y.; Longman, R. S.; Rastinejad, F.; Devlin, A. S.; Krout, M. R.; Fischbach, M. A.; Littman, D. R.; Huh, J. R. <em>Nature<\/em><b> 2019<\/b>, <em>575<\/em>, 143-148; DOI: 10.1038\/s41586-019-1785-z. [<a href=\"https:\/\/static-content.springer.com\/esm\/art%3A10.1038%2Fs41586-019-1785-z\/MediaObjects\/41586_2019_1785_MOESM1_ESM.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<br><br>\n<a href=\"https:\/\/www.biorxiv.org\/content\/10.1101\/465344v1\">Preprint<\/a> uploaded to <em>Biorxiv<\/em> on November 8, 2018.<br><a href=\"https:\/\/www.nature.com\/articles\/s41586-019-1785-z\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" title=\"Bile acid metabolites control Tcells\" src=\"http:\/\/krout.scholar.bucknell.edu\/files\/2019\/11\/Nature2019-e1575046425838.jpeg\"><\/a><\/li>\n<li class=\"publications\" value=\"13\">&#8220;<a href=\"https:\/\/www.jove.com\/video\/59775\/efficient-synthesis-all-carbon-quaternary-centers-via-conjugate\" target=\"_blank\" rel=\"noopener noreferrer\">Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides<\/a>,&#8221; Fulton, T. J.*; Townsend, K. M.*; Krout, M. R. <em>J. Visualized Exp.<\/em><b> 2019<\/b>, <em>147<\/em>, e59775; DOI: 10.3791\/59775.<br><iframe loading=\"lazy\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" src=\"https:\/\/www.jove.com\/embed\/player?id=59775&amp;access=zxqcrex5&amp;s=1\" width=\"368\" height=\"292\" frameborder=\"0\" marginwidth=\"0\" scrolling=\"no\" allowfullscreen=\"allowfullscreen\"><a title=\"Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides\" href=\"https:\/\/www.jove.com\/video\/59775\/efficient-synthesis-all-carbon-quaternary-centers-via-conjugate\">Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides<\/a>\n<p><\/p><\/iframe><\/li>\n<li class=\"publications\" value=\"12\">&#8220;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.8b02201\" target=\"_blank\" rel=\"noopener noreferrer\">Access to Functionalized Quaternary Stereocenters via the Copper-Catalyzed Conjugate Addition of Monoorganozinc Bromide Reagents Enabled by <em>N,N<\/em>-Dimethylacetamide<\/a>,&#8221; Fulton, T. J.*; Alley, P. L.*; Rensch, H. R.; Ackerman, A. M.*; Berlin, C. B.*; Krout, M. R. <em>J. Org. Chem.<\/em><b> 2018<\/b>, <em>83<\/em>, 14723\u201314732; DOI: 10.1021\/acs.joc.8b02201. [<a href=\"https:\/\/pubs.acs.org\/doi\/suppl\/10.1021\/acs.joc.8b02201\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<br><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.8b02201\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" title=\"Cu-catalyzed RZnBr Conjugate Additions\" src=\"https:\/\/pubs.acs.org\/na101\/home\/literatum\/publisher\/achs\/journals\/content\/joceah\/2018\/joceah.2018.83.issue-23\/acs.joc.8b02201\/20181130\/images\/medium\/jo-2018-02201u_0009.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"11\">&#8220;<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.7b02972\" target=\"_blank\" rel=\"noopener noreferrer\">Wolff\/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin<\/a>,&#8221; Krout, M. R.; Henry, C. E.; Jensen, T.; Wu, K.-L.; Virgil, S. R.; Stoltz, B. M. <em>J. Org. Chem.<\/em><b> 2018<\/b>, <em>83<\/em>, 6995\u20137009; DOI: 10.1021\/acs.joc.7b02972. [<a href=\"http:\/\/pubs.acs.org\/doi\/suppl\/10.1021\/acs.joc.7b02972\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.7b02972\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"width: 42%; height: 42%; padding-top: 0.5em;\" title=\"Wolff\/Cope Approach to Variecolin\" src=\"https:\/\/pubs.acs.org\/na101\/home\/literatum\/publisher\/achs\/journals\/content\/joceah\/2018\/joceah.2018.83.issue-13\/acs.joc.7b02972\/20180628\/images\/medium\/jo-2017-02972p_0017.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"10\">&#8220;<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ic5024357\" target=\"_blank\" rel=\"noopener noreferrer\">Resolved P-Metalated Nucleoside Phosphoramidites<\/a>,&#8221; Miller, E. J.*; Garcia, K. J.*; Holahan, E. C.*; Ciccarelli, R. M.*; Bergin, R. A.*; Casino, S. L.*; Bogaczyk, T. L.*; Krout, M. R.; Findeis, P. M.; Stockland, Jr., R. A. <em>Inorg. Chem.<\/em><b> 2014<\/b>, <em>53<\/em>, 12680\u201312682; DOI: 10.1021\/ic5024357. [<a href=\"http:\/\/pubs.acs.org\/doi\/suppl\/10.1021\/ic5024357\/suppl_file\/ic5024357_si_001.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ic5024357\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"width: 42%; height: 42%; padding-top: 0.5em;\" title=\"Resolved P-Metalated Nucleoside Phosphoramidites.\" src=\"https:\/\/pubs.acs.org\/na101\/home\/literatum\/publisher\/achs\/journals\/content\/inocaj\/2014\/inocaj.2014.53.issue-24\/ic5024357\/20141209\/images\/medium\/ic-2014-024357_0004.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"9\">\u201c<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402011015870\" target=\"_blank\" rel=\"noopener noreferrer\">Palladium-Catalyzed Asymmetric Alkylation in the Synthesis of Cyclopentanoid and Cycloheptanoid Core Structures Bearing All-Carbon Quaternary Stereocenters<\/a>,&#8221; Hong, A. Y.; Bennett, N. B.; Krout, M. R.; Jensen, T.; Harned, A. M.; Stoltz, B. M. <em>Tetrahedron<\/em><b> 2011<\/b>, <em>67<\/em>, 10234\u201310248; DOI: 10.1016\/j.tet.2011.10.031. [<a href=\"http:\/\/www.sciencedirect.com\/science\/MiamiMultiMediaURL\/1-s2.0-S0040402011015870\/1-s2.0-S0040402011015870-mmc1.pdf\/271372\/html\/S0040402011015870\/b8afe4ae31ec6f1972190be968d1bf2d\/mmc1.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402011015870\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"padding-top: 0.5em;\" title=\"Palladium-Catalyzed Asymmetric Alkylation in the Synthesis of Cyclopentanoid and Cycloheptanoid Core Structures Bearing All-Carbon Quaternary Stereocenters.\" src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0040402011015870-fx1.jpg\"><\/a><\/li>\n<li class=\"publications\" value=\"8\">&#8220;<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201003383\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Enantioselective Decarboxylative Alkylation Reactions: Catalyst Development, Substrate Scope, and Mechanistic Studies<\/a>,&#8221; Behenna, D. C.; Mohr, J. T.; Sherden, N. H.; Marinescu, S. C.; Harned, A. M.; Tani, K.; Seto, M.; Ma, S.; Nov\u00e1k, Z; Krout, M. R.; McFadden, R. M.; Roizen, J. L., Enquist, Jr., J. A.; White, D. E.; Levine, S. R.*; Petrova, K. V.*; Iwashita, A.; Virgil, S. C.; Stoltz, B. M. <em>Chem.\u2014Eur. J.<\/em><b> 2011<\/b>, <em>17<\/em>, 14199\u201314223; DOI: 10.1002\/chem.201003383. [<a href=\"http:\/\/onlinelibrary.wiley.com\/store\/10.1002\/chem.201003383\/asset\/supinfo\/chem_201003383_sm_miscellaneous_information.pdf?v=1&amp;s=c0d1efb9e67f1bae4a46a8fa9f99df7cf49e7e1f\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<\/li>\n<li class=\"publications\" value=\"7\">&#8220;<a href=\"http:\/\/www.nature.com\/nature\/journal\/v472\/n7344\/abs\/nature09978.html\" target=\"_blank\" rel=\"noopener noreferrer\">Digoxin and its derivatives suppress TH17 cell differentiation by antagonizing ROR\u03b3t activity<\/a>,&#8221; Huh, J. R.; Leung, M. W. L.; Huang, P.; Ryan, D. A.; Krout, M. R.; Malapaka, R. R. V.; Chow, J.; Manel, N.; Ciofani, M.; Kim, S. V.; Cuesta, A.; Santori, F. R.; Lafaille, J. J.; Xu, H. E.; Gin, D. Y.; Rastinejad, F.; Littman, D. R. <em>Nature<\/em> <b>2011<\/b>, <em>472<\/em>, 486\u2013490; DOI: 10.1038\/nature09978. [<a href=\"http:\/\/www.nature.com\/nature\/journal\/v472\/n7344\/extref\/nature09978-s1.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/www.nature.com\/nature\/journal\/v472\/n7344\/abs\/nature09978.html\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter size-large\" style=\"width: 346.5px; height: 275.9px; padding-top: 0.5em;\" title=\"Digoxin and its derivatives suppress TH17 cell differentiation by antagonizing ROR\u03b3t activity.\" src=\"http:\/\/krout.scholar.bucknell.edu\/files\/2021\/02\/nature2009_486-image1-e1612737854905.jpg\"><\/a><\/li>\n<li class=\"publications\" value=\"6\">&#8220;<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201007814\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Ring-Contraction Strategy for the Practical, Scalable, Catalytic Asymmetric Synthesis of Versatile \u03b3-Quaternary Acylcyclopentenes<\/a>,&#8221; Hong, A. Y.; Krout, M. R.; Jensen, T.; Bennett, N. B.; Harned, A. M.; Stoltz, B. M. <em>Angew. Chem., Int. Ed.<\/em><b> 2011<\/b>, <em>50<\/em>, 2756\u20132760; DOI: 10.1002\/anie.201007814. [<a href=\"http:\/\/onlinelibrary.wiley.com\/store\/10.1002\/anie.201007814\/asset\/supinfo\/anie_201007814_sm_miscellaneous_information.pdf?v=1&amp;s=f2aab30fcbf4213205f36ccc33f1d52fb4c3aca0\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201007814\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"width: 55%; height: 55%; padding-top: 0.5em;\" title=\"Practical, Scalable, Catalytic Asymmetric Synthesis of Versatile \u03b3-Quaternary Acylcyclopentenes.\" src=\"https:\/\/wol-prod-cdn.literatumonline.com\/cms\/attachment\/2f71a5fd-74af-407b-9798-ac827a9f77bb\/mcontent.jpg\"><\/a><\/li>\n<li class=\"publications\" value=\"5\">&#8220;<a href=\"https:\/\/doi.org\/10.15227\/orgsyn.086.0194\" target=\"_blank\" rel=\"noopener noreferrer\">Preparation of <em>(S)<\/em>-2-allyl-2-methylcyclohexanone (Cyclohexanone, 2-methyl-2-(2-propen-1-yl)-, <em>(2S)<\/em>-)<\/a>,&#8221; Mohr, J. T.; Krout, M. R.; Stoltz, B. M. <em>Org. Synth.<\/em><b> 2009<\/b>, <em>86<\/em>, 194\u2013211; DOI: 10.15227\/orgsyn.086.0194.<a href=\"https:\/\/doi.org\/10.15227\/orgsyn.086.0194\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter size-small\" style=\"padding-top: 0.5em;\" title=\"Preparation of (S)-2-allyl-2-methylcyclohexanone.\" src=\"http:\/\/orgsyn.org\/content\/figures\/V86P0194-1.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"4\">&#8220;<a href=\"https:\/\/doi.org\/10.15227\/orgsyn.086.0181\" target=\"_blank\" rel=\"noopener noreferrer\">Preparation of <em>(S)<\/em>&#8211;<em>tert<\/em>-ButylPHOX (Oxazole, 4-(1,1-dimethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro- <em>(4S)<\/em>-)<\/a>,&#8221; Krout, M. R.; Mohr, J. T.; Stoltz, B. M. <em>Org. Synth.<\/em><b> 2009<\/b>, <em>86<\/em>, 181\u2013193; DOI: 10.15227\/orgsyn.086.0181.<a href=\"https:\/\/doi.org\/10.15227\/orgsyn.086.0181\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter size-small\" style=\"padding-top: 0.5em;\" title=\"Preparation of (S)-tert-butylPHOX.\" src=\"http:\/\/orgsyn.org\/content\/figures\/V86P0181-1.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"3\">&#8220;<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ol802409h\" target=\"_blank\" rel=\"noopener noreferrer\">Catalytic Enantioselective Approach to the Eudesmane Sesquiterpenoids: Total Synthesis of (+)-Carissone<\/a>,&#8221; Levine, S. R.*; Krout, M. R.; Stoltz, B. M. <em>Org. Lett.<\/em> <b>2009<\/b>, <em>11<\/em>, 289\u2013292; DOI: 10.1021\/ol802409h. [<a href=\"http:\/\/pubs.acs.org\/doi\/suppl\/10.1021\/ol802409h\/suppl_file\/ol802409h_si_001.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ol802409h\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter size-small\" style=\"width: 42%; height: 42%; padding-top: 0.5em;\" title=\"Catalytic Enantioselective Approach to the Eudesmane Sesquiterpenoids.\" src=\"https:\/\/pubs.acs.org\/na101\/home\/literatum\/publisher\/achs\/journals\/content\/orlef7\/2009\/orlef7.2009.11.issue-2\/ol802409h\/production\/images\/medium\/ol-2008-02409h_0007.gif\"><\/a><\/li>\n<li class=\"publications\" value=\"2\">&#8220;<a href=\"http:\/\/www.nature.com\/nature\/journal\/v455\/n7211\/abs\/nature07370.html\" target=\"_blank\" rel=\"noopener noreferrer\">Natural products as inspiration for the development of asymmetric catalysis<\/a>,&#8221; Mohr, J. T.; Krout, M. R.; Stoltz, B. M. <em>Nature<\/em> <b>2008<\/b>, <em>455<\/em>, 323\u2013332; DOI: 10.1038\/nature07370.<\/li>\n<li class=\"publications\" value=\"1\">&#8220;<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ja067703m\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis of 2-Quinuclidonium by Eliminating Water: Experimental Quantification of the High Basicity of Extremely Twisted Amides<\/a>,&#8221; Ly, T.; Krout, M.; Pham, D. K.; Tani, K.; Stoltz, B. M.; Julian, R. M. <em>J. Am. Chem. Soc.<\/em> <b>2007<\/b>, <em>129<\/em>, 1864\u20131865; DOI: 10.1021\/ja067703m. [<a href=\"http:\/\/pubs.acs.org\/doi\/suppl\/10.1021\/ja067703m\/suppl_file\/ja067703msi20070118_030344.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">supporting information<\/a>]<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ja067703m\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" class=\"aligncenter\" style=\"width: 35%; height: 35%; padding-top: 0.5em;\" title=\"Synthesis of 2-Quinuclidonium by Eliminating Water.\" src=\"https:\/\/pubs.acs.org\/na101\/home\/literatum\/publisher\/achs\/journals\/content\/jacsat\/2007\/jacsat.2007.129.issue-7\/ja067703m\/production\/images\/medium\/ja067703mn00001.gif\"><\/a><\/li>\n<\/ol>\n<hr>\n<p><strong>Patents<\/strong><\/p>\n<ol>\n<li class=\"publications\" value=\"2\">Littman, D. R; Huh, J. R.; Manel, N. G. A.; Gin, D. Y.; Krout, M. R.; Ryan, D. A. &#8220;<a href=\"https:\/\/patents.google.com\/patent\/US20140066391A1\/en\" target=\"_blank\" rel=\"noopener noreferrer\">Steroid Compounds as ROR\u03b3t Modulators and Uses Thereof<\/a>,&#8221; U.S. Patent 20140066391 A1, March 6, 2014.<\/li>\n<li class=\"publications\" value=\"1\">Hanney, B.; Kim, Y.; Krout, M. R.; Meissner, R. S.; Mitchell, H. J.; Musselman, J.; Perkins, J. J.; Wang, J. &#8220;<a href=\"https:\/\/patents.google.com\/patent\/US20050277681A1\/en\" target=\"_blank\" rel=\"noopener noreferrer\"><i>N<\/i>-Benzyl-2-phenylbutanamides as tissue-selective androgen modulators, their preparation, pharmaceutical compositions, and use in therapy<\/a>,&#8221; U.S. Patent 20050277681 A1, December 15, 2005.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Peer-Reviewed Publications (* indicates undergraduate authors) \u2003 [view non-graphical list] &#8220;Determining sequential micellization steps of bile salts with multi-CMC modeling,&#8221; Rovnyak, D.; He, J.*; Kong,&#8230;<\/p>\n<div class=\"more-link-wrapper\"><a class=\"more-link\" href=\"https:\/\/krout.scholar.bucknell.edu\/?page_id=40\">Continue reading<span class=\"screen-reader-text\">research publications<\/span><\/a><\/div>\n","protected":false},"author":3719,"featured_media":123,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-40","page","type-page","status-publish","has-post-thumbnail","hentry","entry"],"_links":{"self":[{"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/pages\/40","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/users\/3719"}],"replies":[{"embeddable":true,"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=40"}],"version-history":[{"count":148,"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/pages\/40\/revisions"}],"predecessor-version":[{"id":1161,"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/wp\/v2\/pages\/40\/revisions\/1161"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=\/"}],"wp:attachment":[{"href":"https:\/\/krout.scholar.bucknell.edu\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=40"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}