{"id":2233,"date":"2018-08-30T19:18:04","date_gmt":"2018-08-30T19:18:04","guid":{"rendered":"http:\/\/commons.trincoll.edu\/chemistry\/?page_id=2233"},"modified":"2018-08-31T14:31:36","modified_gmt":"2018-08-31T14:31:36","slug":"2017-2","status":"publish","type":"page","link":"http:\/\/commons.trincoll.edu\/chemistry\/publications\/2017-2\/","title":{"rendered":"Publications from 2017"},"content":{"rendered":"<p>Boekell, N. G.; Cerone, D. J.; Boucher, M. M.; Quach, P. K.; Nganyak Tentchou, W. B.; Reavis, C. G.; Okoh, I. I.; Reid, J. O. A.; Berg, H. E.; Chang, B. A.; Brindle, C. S. 2017. Triarylmethyl Cation Catalysis: A Tunable Lewis Acid Organocatalyst for the Synthesis of Bisindolylmethanes<em>. <\/em><em>SynOpen.<\/em> <strong>1<em>: <\/em><\/strong>97\u2013102. <strong>DOI<\/strong>:\u00a0<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1588559\">10.1055\/s-0036-1588559<\/a><\/p>\n<p>Boucher, M. M.; Furigay, M. H.; Quach, P. K.; Brindle, C. S. 2017. Liquid-Liquid Extraction Protocol for the Removal of Aldehydes and Highly Reactive Ketones from Mixtures. \u00a0<em>Org. Process Res. Dev.<\/em> <strong>21<\/strong>: 1394\u20131403. <strong>DOI<\/strong>:\u00a0<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.oprd.7b00231\">10.1021\/acs.oprd.7b00231<\/a><\/p>\n<p>Tierney, A. J.; Pham, N.; Yang, K.; Emerick, B. K.; Kovarik, M. L. 2017. Interspecies Comparison of Peptide Substrate Reporter Metabolism Using Compartment-Based Modeling. <i>Analytical and Bioanalytical Chemistry<\/i>, <b>409<\/b>: 1173-1183. <strong>DOI<\/strong>: <span class=\"bibliographic-informationvalue\"><a id=\"LPlnk277201\" class=\"OWAAutoLink\" href=\"https:\/\/doi.org\/10.1007\/s00216-016-0085-9\">10.1007\/s00216-016-0085-9<\/a><\/span><\/p>\n<p>Curran, T. P.; Lawrence, A. P.; Murtaugh, T. S.; Ji, W.; Pokharel, N.; Gober, C. G.; Suitor, J. 2017. Conformationally Rigid Cyclic Tungsten Bis-Alkyne Complexes Derived from 1,1&#8242;-Dialkynylferrocenes. <em>J. Organometallic Chem.,<\/em> <strong>846<\/strong>:\u00a024-32. <strong>DOI<\/strong>:<a class=\"doi\" title=\"Persistent link using digital object identifier\" href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2017.05.048\" target=\"_blank\" rel=\"noopener\">10.1016\/j.jorganchem.2017.05.048<\/a><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Boekell, N. G.; Cerone, D. J.; Boucher, M. M.; Quach, P. K.; Nganyak Tentchou, W. B.; Reavis, C. G.; Okoh, I. I.; Reid, J. O. A.; Berg, H. E.; Chang, B. A.; Brindle, C. S. 2017. Triarylmethyl Cation Catalysis: A Tunable Lewis Acid Organocatalyst for the Synthesis of Bisindolylmethanes. SynOpen. 1: 97\u2013102. DOI:\u00a010.1055\/s-0036-1588559 Boucher, M. [&hellip;]<\/p>\n","protected":false},"author":166,"featured_media":0,"parent":19,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/pages\/2233"}],"collection":[{"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/users\/166"}],"replies":[{"embeddable":true,"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/comments?post=2233"}],"version-history":[{"count":7,"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/pages\/2233\/revisions"}],"predecessor-version":[{"id":2257,"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/pages\/2233\/revisions\/2257"}],"up":[{"embeddable":true,"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/pages\/19"}],"wp:attachment":[{"href":"http:\/\/commons.trincoll.edu\/chemistry\/wp-json\/wp\/v2\/media?parent=2233"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}