{"id":47,"date":"2016-05-24T17:00:32","date_gmt":"2016-05-24T21:00:32","guid":{"rendered":"http:\/\/blog.richmond.edu\/downey\/?page_id=47"},"modified":"2025-05-12T12:53:51","modified_gmt":"2025-05-12T16:53:51","slug":"former-group-members","status":"publish","type":"page","link":"https:\/\/blog.richmond.edu\/downey\/former-group-members\/","title":{"rendered":"Former Group Members"},"content":{"rendered":"<p>Daniel Lawrence &#8217;07 &#8211; Aldol reactions of acetic acid<\/p>\n<p>Ryan Sault &#8217;07 &#8211; Intramolecular conjugate addition-Diels\u2013Alder sequences<\/p>\n<p>Eric Etchill &#8217;07 &#8211; Conjugate additions of nitroalkanes to ethyl propiolate<\/p>\n<p>Brian Southall &#8217;07 &#8211; Conjugate additions of thiols to ethyl propiolate<\/p>\n<p>Katie Tracy &#8217;08 &#8211; Aldol reactions of acetic acid; aldol-type additions to acetals<\/p>\n<p>Odamea Akomah &#8217;09 &#8211; Addition of ketones to nitrones<\/p>\n<p>Steph Corsi &#8217;09 &#8211; Conjugate addition-Diels\u2013Alder sequences<\/p>\n<p>Miles Johnson &#8217;09 &#8211; Aldol reactions of ketones; aldol reactions of acetic acid; aldol-type additions to acetals<\/p>\n<p>Brian Mahoney &#8217;09 &#8211; Zinc acetylide additions to aldehydes<\/p>\n<p>Vin Lipari &#8217;10 &#8211; Zinc acetylide additions to aldehydes<\/p>\n<p>Dave Widmayer &#8217;10 &#8211; Intramolecular conjugate addition-Diels\u2013Alder sequences<\/p>\n<p>Smaranda Craciun &#8217;11 &#8211; Conjugate addition-Diels\u2013Alder sequences<\/p>\n<p>Alan Fleisher &#8217;11 &#8211; Aldol reactions of carboxylic acids; N,O-acetalization reactions of N-phenyl amides<\/p>\n<p>Jimmy Rague &#8217;11 &#8211; N,O-acetalization reactions of N-phenyl amides, alkyne additions to acetals, methyl ether electrophiles<\/p>\n<p>Megan Venable &#8217;11 &#8211; N,O-acetalization reactions of N-phenyl amides<\/p>\n<p>Chelsea Safran &#8217;12 &#8211; N,O-acetalization reactions of N-phenyl amides, addition of ketones to nitrones<\/p>\n<p>Christina Vivelo &#8217;12 &#8211; Conjugate addition-Diels\u2013Alder sequences<\/p>\n<p>Sarah Covington &#8217;13 &#8211; Methyl ether electrophiles<\/p>\n<p>Ana Neferu &#8217;13 &#8211; Conjugate addition-Diels\u2013Alder sequences, additions of secondary amines to ethyl propiolate<\/p>\n<p>Rohina Sediqui &#8217;13 &#8211; Aldol reactions of thioesters<\/p>\n<p>Carolyn Dombrowski &#8217;14 &#8211; Addition of ketones to nitrones, addition of ketones to imines<\/p>\n<p>Evan Halliday &#8217;14 &#8211; Methyl ether electrophiles<\/p>\n<p>Jimmy Maiarana &#8217;14 &#8211; Aldol reactions of ketones<\/p>\n<p>Erin Maxwell &#8217;14 &#8211; Addition of thioesters to nitrones, addition of zinc acetylides to nitrones<\/p>\n<p>Carly Mueller &#8217;14 &#8211; Conjugate addition-Diels\u2013Alder sequences, addition of silylnitriles to aldehydes<\/p>\n<p>Alissa Nizinski &#8217;14 &#8211; Addition of indoles to aldehydes<\/p>\n<p>Derek Obenschain &#8217;14 &#8211; Methyl ether electrophiles<\/p>\n<p>Adam Barnett &#8217;15 &#8211; Alpha-oxygenation of ketones<\/p>\n<p>Courtney Botelho &#8217;15 &#8211; Addition of silylnitriles to acetals<\/p>\n<p>Jared Ingersoll &#8217;15 &#8211; Aldol additions of thioesters, addition of thioesters to imines<\/p>\n<p>Nick Yeutter &#8217;15 &#8211; Epoxide openings with halides<\/p>\n<p>Danielle Confair &#8217;16 &#8211; Methyl ether electrophiles, addition of zinc acetylides to nitrones, alkylation of ketones with propargyl carboxylates<\/p>\n<p>Hadleigh Glist &#8217;16 &#8211; Addition of amides, esters, and ketones to imines; chalcone formation reactions<\/p>\n<p>Alice Lee &#8217;16 &#8211; Addition of silylnitriles to aldehydes and acetals<\/p>\n<p>Ken MacCormac &#8217;16 &#8211; Aldol additions in ethyl acetate<\/p>\n<p>Chris Poff &#8217;17 &#8211; Addition of indoles to aldehydes and nitrones<\/p>\n<p>Matt Santa &#8217;17 &#8211; Addition of acetonitrile to nitrones<\/p>\n<p>Anna Takashima &#8217;17 &#8211; Chalcone formation reactions and aldol additions in ethyl acetate<\/p>\n<p>Jack Goodin &#8217;18 &#8211; Condensations of TMS-acetonitrile with acetals<\/p>\n<p>Alethea Lin &#8217;18 &#8211; One-pot enol silane formation-alkylation reactions of ketones with allyl acetates<\/p>\n<p>Yiqi Liu &#8217;18 &#8211;\u00a0Alkylation of ketones with propargyl carboxylates<\/p>\n<p>William Stith &#8217;18 &#8211; Addition of nitriles and silylnitriles to acetals<\/p>\n<p>Kylie Britt &#8217;19 &#8211; TMSOTf-mediated additions of TMS-acetonitrile to aldehydes.<\/p>\n<p>Kari Flicker &#8217;19 &#8211; Addition of acetonitrile to nitrones<\/p>\n<p>Elizabeth Heafner &#8217;19 &#8211; One-pot enol silane formation-alkylation reactions of ketones<\/p>\n<p>Zach Oracheff &#8217;19 &#8211; Friedel\u2013Crafts additions of indoles to nitrones<\/p>\n<p>Sam Bottum &#8217;20 &#8211; Aldol condensations and nitrile aldol reactions<\/p>\n<p>Grant Dixon &#8217;20 &#8211; Aldehyde-aldehyde aldol coupling and styrene synthesis<\/p>\n<p>Kevin Kim &#8217;20 &#8211; \u00a0TMSOTf-promoted reactions of acylated oxazolidinones<\/p>\n<p>Dani Sklar &#8217;20 &#8211; One-pot furan synthesis<\/p>\n<p>Claire Fuller &#8217;21 &#8211; Aldol reactions in ester solvents, aziridine-opening reactions<\/p>\n<p>Scott Isaacson &#8217;21 &#8211; Friedel\u2013Crafts additions of indoles to nitrones<\/p>\n<p>Grace Ann Robertson &#8217;21 &#8211; Addition of acetonitrile to nitrones and acetals<\/p>\n<p>Hanyu &#8220;Ivy&#8221; Zhong &#8217;21 &#8211; One-pot enol silane formation-allylation reactions<\/p>\n<p>Bianca Bicalho &#8217;22 &#8211; Indole alkylations<\/p>\n<p>Ramsey Goodner &#8217;22 &#8211; Synthesis of 2,3-dihydroisoxazoles<\/p>\n<p>Ryan Kern &#8217;22 &#8211; Friedel\u2013Crafts addition of indoles to nitrones<\/p>\n<p>Michael Rodriguez &#8217;22 &#8211; Styrene synthesis<\/p>\n<p>Tyler Chong &#8217;23 &#8211; N-alkylation of amides with propargyl propionates, styrene synthesis<\/p>\n<p>Joseph Coyle &#8217;23 &#8211; One-pot enol silane formation-allylation reactions<\/p>\n<p>Alex Helbling &#8217;23 &#8211; One-pot furan synthesis, N-alkylation of amides with propargyl propionates<\/p>\n<p>Mohamad Hussein &#8217;23 &#8211; One-pot silyl imidate formation-allylation reactions<\/p>\n<p>Olivia Lambertson &#8217;23 &#8211; Mannich addition-reduction sequences of N-benzyl nitrones<\/p>\n<p>Alexa Connors &#8217;24 &#8211; One-pot enol silane formation-allylation reactions<\/p>\n<p>Greg Hughes &#8217;24 &#8211; Synthesis of 4-isoxazolines<\/p>\n<p>Helen Xia &#8217;24 &#8211; Friedel\u2013Crafts additions of indoles to nitrones, Friedel\u2013Crafts alkylations of indoles and benzofuran<\/p>\n<p>Karmen Smith &#8217;25 &#8211; One-pot enol silane formation-alkylation reactions of ketones<\/p>\n<p>Katie Marchione &#8217;25 &#8211; One-pot enol silane formation-alkylation reactions of ketones<\/p>\n<p>Joshua Pae &#8217;25 &#8211; N-Propargylation of carbamates<\/p>\n<p>Lauren Rausch &#8217;25 &#8211; Povarov cyclization of 4-isoxazolines<\/p>\n<p>Mark Strigel &#8217;25 &#8211; Mannich addition-reduction sequences of N-benzyl nitrones, Synthesis of 4-isoxazolines<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Daniel Lawrence &#8217;07 &#8211; Aldol reactions of acetic acid Ryan Sault &#8217;07 &#8211; Intramolecular conjugate addition-Diels\u2013Alder sequences Eric Etchill &#8217;07 &#8211; Conjugate additions of nitroalkanes to ethyl propiolate Brian Southall &#8217;07 &#8211; Conjugate additions of thiols to ethyl propiolate Katie<\/p>\n","protected":false},"author":2955,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-47","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/pages\/47","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/users\/2955"}],"replies":[{"embeddable":true,"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/comments?post=47"}],"version-history":[{"count":10,"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/pages\/47\/revisions"}],"predecessor-version":[{"id":342,"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/pages\/47\/revisions\/342"}],"wp:attachment":[{"href":"https:\/\/blog.richmond.edu\/downey\/wp-json\/wp\/v2\/media?parent=47"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}