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Mnemonic use for aiding students to determine erythro vs threo stereochemistry in additions to internal alkenes John H. MacMillan Ph.D. Department of Chemistry, Temple University, Philadelphia, Pa

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GRANVILLE ISLAND SCHEDULE 6:00 PM PROCESSION • Granville Island Triangle Square – Carnival Band • Leg-in-Boot-Square – Bloco Energia • H.R. MacMillan Space Centre – Rhythm Spirit Drummers

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In situ propargylic Grignard addition to vinylic ketone; 3-Methyl-1-hexene-5-yn-3-ol John H. MacMillan Department of Chemistry, Temple University, Philadelphia, Pa

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Managing Red Hat Enterprise Linux 5 Daniel J Walsh SELinux Lead Engineer Karl MacMillan

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Synthesis of Additional 4 and 5-Aryl Substituted 1,3(3H) Oxazine-2,6-Diones. John H. MacMillan and Stephen S. Washburne Department of Chemistry, Temple University, Philadelphia, PaThe following additional 4-and 5

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Allyl Grignard addition to the internal alkyne carbon of propargyl alcohol; 2-Methylene-4-penten-1-ol Synthetic Page 596 Submitted Jun 02, 2013, published Jun 07, 2013 John MacMillan ()

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Investigation of Possible Phenyl Participation in the Oxy-Cope and Acetylenic Oxy-Cope Rearrangements By John H. MacMillan and Alfred Viola Department of Chemistry Northeastern University

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Mild esterification with diazomethane; Methyl-2E,4E-hexadienoate Synthetic Page 701 Submitted Nov 12, 2013, published Nov 13, 2013 DOI: SP701 John MacMillan ()

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