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By:Kari Plog '11 and Karen Miller September 12, 2018 0 Wall Street State of Mind https://www.plu.edu/resolute/fall-2018/wp-content/uploads/sites/27/2018/09/pape-samba-msf-cover-1024x532.jpg 1024 532 Kari Plog '11 and Karen Miller Kari Plog '11 and Karen Miller https://secure.gravatar.com/avatar/a28c2c7716b27b7026f8295c44c19861?s=96&d=mm&r=g September 12, 2018 October 3, 2018 Wall Street State of Mind A younger Pape Samba ’18 watched movies and news stories from his home in Senegal and became

conflict and water as a vital resource in the struggle against poverty. 4:30-5:30 p.m. Our Thirsty Planet – Reactions and Community Action – 208 Garfield Following the Wang Center Symposium, head on over to 208 on Garfield Street to chat about your reactions to what impacted you from the speakers’ presentations. This will also be an opportunity to connect with others working on sustainability issues such as PLU’s GREAN student club and to be a part of the conversation about what actions we can take as

viability of iodobenzene diacetate as an oxidizing agent for in-situ “ene”-reactions to synthesize nitroso compounds. Green Synthesis of Hydroxyureas from DMDTC Dana L. Hiett, Senior Capstone Seminar Hydroxyureas have been used in medicine since the mid 1900’s, and the biological impacts of these molecules have been widely studied in relation to tumor suppression,  alleviation of sickle cell disease symptoms, and many others. As the medicinal properties of these compounds have been discovered and tested

what we eat Throughout the symposium, keep an eye out for facts about water in the University Center Commons. Our Thirsty Planet – Reaction and Community Action – 4:30-5:30 p.m. Friday, Feb. 24 at 208 Garfield Following the Wang Center Symposium, head on over to 208 on Garfield Street to chat about your reactions to what impacted you from the speakers’ presentations. This will also be an opportunity to connect with others working on sustainability issues such as PLU’s GREAN student club and to be a

(isoxazolidine urea). Multiple routes to isoxazolidine urea were studied. In general there are two ways to make derivatized ureas. 1) Make the ureas first, then substitute the urea or 2) substitute the nitrogen nucleophile first then react it with a carbonic acid derivative. Optimization of one synthesis of isoxazolidine urea was completed. The limiting factors that were  discovered to cause low yielding reactions of the optimized route were purity of reagents and the hygroscopicity of a key intermediate