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You searched for +publisher:"University of Notre Dame" +contributor:("Paul Helquist, Committee Chair"). Showing records 1 – 6 of 6 total matches.

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University of Notre Dame

1. Jeffrey Munson Carney. Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>.

Degree: PhD, Chemistry and Biochemistry, 2009, University of Notre Dame

  The intramolecular hydroamination reaction is among the more versatile means of forming nitrogen-containing hetereocycles, compounds of interest in a variety of chemical disciplines. While… (more)

Subjects/Keywords: hydroamination; transition metal catalysis; synthesis; unnatural amino acid; ketoimine; prochiral aminodiyne

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Carney, J. M. (2009). Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/dj52w378667

Chicago Manual of Style (16th Edition):

Carney, Jeffrey Munson. “Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/dj52w378667.

MLA Handbook (7th Edition):

Carney, Jeffrey Munson. “Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>.” 2009. Web. 26 Jun 2019.

Vancouver:

Carney JM. Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/dj52w378667.

Council of Science Editors:

Carney JM. Intramolecular Hydroamination of Alkynes Catalyzed by Silver-Phenanthroline Complexes</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/dj52w378667


University of Notre Dame

2. Kyle Chormanski. Alkyne Substituent Effects in Radicals and Carbocations</h1>.

Degree: MS, Chemistry and Biochemistry, 2010, University of Notre Dame

  Alkyne substituent effects in the methylenecyclopropane rearrangement as well as solvolysis studies of the structurally similar trifluoroacetates were determined. The results of these kinetic… (more)

Subjects/Keywords: kinetics; sigma scale; Methylenecyclopropane rearrangement; rate study

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APA (6th Edition):

Chormanski, K. (2010). Alkyne Substituent Effects in Radicals and Carbocations</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/n583xs57z1t

Chicago Manual of Style (16th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Masters Thesis, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/n583xs57z1t.

MLA Handbook (7th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Web. 26 Jun 2019.

Vancouver:

Chormanski K. Alkyne Substituent Effects in Radicals and Carbocations</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2010. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/n583xs57z1t.

Council of Science Editors:

Chormanski K. Alkyne Substituent Effects in Radicals and Carbocations</h1>. [Masters Thesis]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/n583xs57z1t


University of Notre Dame

3. Casey Cosner. Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>.

Degree: PhD, Chemistry and Biochemistry, 2011, University of Notre Dame

  Niemann-Pick type C disease (NPC) is a rare, fatal, autosomal recessive lipid storage disorder. There is currently no cure for NPC and very few… (more)

Subjects/Keywords: trichostatin A; alkenylation; thiadiazoles; palladium; NPC; Niemann-Pick type C disease; pyrrolinones

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APA (6th Edition):

Cosner, C. (2011). Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/73666397v6g

Chicago Manual of Style (16th Edition):

Cosner, Casey. “Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>.” 2011. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/73666397v6g.

MLA Handbook (7th Edition):

Cosner, Casey. “Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>.” 2011. Web. 26 Jun 2019.

Vancouver:

Cosner C. Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2011. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/73666397v6g.

Council of Science Editors:

Cosner C. Potential Niemann-Pick Type C Disease Therapeutics: Synthesis of Pyrrolinones and Enolate-Derived Thiadiazoles, and the Development of a Palladium-Catalyzed Alpha Alkenylation Reaction as a Means to Prepare Trichostatin A</h1>. [Doctoral Dissertation]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/73666397v6g


University of Notre Dame

4. Pauline Bourbon. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  This thesis describes our endeavors towards the development of therapeutic agents for Niemann-Pick type C disease (NPC), which is a rare, autosomal recessive lipid… (more)

Subjects/Keywords: Cholesterol; Caged compound; Niemann-Pick type C

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APA (6th Edition):

Bourbon, P. (2012). Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b01f5m

Chicago Manual of Style (16th Edition):

Bourbon, Pauline. “Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/0k225b01f5m.

MLA Handbook (7th Edition):

Bourbon, Pauline. “Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.” 2012. Web. 26 Jun 2019.

Vancouver:

Bourbon P. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/0k225b01f5m.

Council of Science Editors:

Bourbon P. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/0k225b01f5m


University of Notre Dame

5. Jacob Matthew Plummer. Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>.

Degree: PhD, Chemistry and Biochemistry, 2008, University of Notre Dame

  1,10-Phenanthroline derivatives are important for a variety of synthetic applications and serve as effective ligands in a wide selection of reactions. While a variety… (more)

Subjects/Keywords: chiral ligands; trichostatin A; conjugate additions

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APA (6th Edition):

Plummer, J. M. (2008). Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/v979v12188z

Chicago Manual of Style (16th Edition):

Plummer, Jacob Matthew. “Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>.” 2008. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/v979v12188z.

MLA Handbook (7th Edition):

Plummer, Jacob Matthew. “Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>.” 2008. Web. 26 Jun 2019.

Vancouver:

Plummer JM. Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2008. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/v979v12188z.

Council of Science Editors:

Plummer JM. Development of New Phenanthroline-Based Chiral Ligands, Asymmetric Additions to Lactams, and the Completion of the Synthesis of Trichostatin A</h1>. [Doctoral Dissertation]. University of Notre Dame; 2008. Available from: https://curate.nd.edu/show/v979v12188z


University of Notre Dame

6. Jamie Lynn Zigterman. Toward the Synthesis of Iejimalide B</h1>.

Degree: MS, Chemistry and Biochemistry, 2004, University of Notre Dame

  This thesis discusses synthetic efforts made toward the total synthesis of the iejimalides (1 and 2a-d). The iejimalides exhibit potent cytotoxicity, however, they are… (more)

Subjects/Keywords: natural product synthesis

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APA (6th Edition):

Zigterman, J. L. (2004). Toward the Synthesis of Iejimalide B</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/9c67wm1390q

Chicago Manual of Style (16th Edition):

Zigterman, Jamie Lynn. “Toward the Synthesis of Iejimalide B</h1>.” 2004. Masters Thesis, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/9c67wm1390q.

MLA Handbook (7th Edition):

Zigterman, Jamie Lynn. “Toward the Synthesis of Iejimalide B</h1>.” 2004. Web. 26 Jun 2019.

Vancouver:

Zigterman JL. Toward the Synthesis of Iejimalide B</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2004. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/9c67wm1390q.

Council of Science Editors:

Zigterman JL. Toward the Synthesis of Iejimalide B</h1>. [Masters Thesis]. University of Notre Dame; 2004. Available from: https://curate.nd.edu/show/9c67wm1390q

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