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You searched for +publisher:"University of Notre Dame" +contributor:("Richard Taylor, Committee Member"). Showing records 1 – 16 of 16 total matches.

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University of Notre Dame

1. Kasey J Clear. Molecular Probes for Biomembrane Recognition</h1>.

Degree: Chemistry and Biochemistry, 2016, University of Notre Dame

  The biological membrane is made up of primarily polar lipids and integral membrane proteins. Polar lipids are a broad class of amphiphilic biomolecules that… (more)

Subjects/Keywords: molecular recognition; anion recognition; cell death; organic chemistry; molecular imaging; lipids; fluorescence

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APA (6th Edition):

Clear, K. J. (2016). Molecular Probes for Biomembrane Recognition</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/dv13zs2842v

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Clear, Kasey J. “Molecular Probes for Biomembrane Recognition</h1>.” 2016. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/dv13zs2842v.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Clear, Kasey J. “Molecular Probes for Biomembrane Recognition</h1>.” 2016. Web. 13 Aug 2020.

Vancouver:

Clear KJ. Molecular Probes for Biomembrane Recognition</h1>. [Internet] [Thesis]. University of Notre Dame; 2016. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/dv13zs2842v.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Clear KJ. Molecular Probes for Biomembrane Recognition</h1>. [Thesis]. University of Notre Dame; 2016. Available from: https://curate.nd.edu/show/dv13zs2842v

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

2. Joseph Bartholomew Gianino. Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>.

Degree: Chemistry and Biochemistry, 2014, University of Notre Dame

  A titanocene catalyst system is described herein for the synthesis of tertiary carbon centers. Using catalytic titanocene, phosphine, and zinc dust, zinc acetylides can… (more)

Subjects/Keywords: titanocene; transition metal catalysis; multicomponent coupling

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APA (6th Edition):

Gianino, J. B. (2014). Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/fj236111169

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gianino, Joseph Bartholomew. “Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>.” 2014. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/fj236111169.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gianino, Joseph Bartholomew. “Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>.” 2014. Web. 13 Aug 2020.

Vancouver:

Gianino JB. Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>. [Internet] [Thesis]. University of Notre Dame; 2014. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/fj236111169.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gianino JB. Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>. [Thesis]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/fj236111169

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

3. Nicholas M. Myers. Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>.

Degree: Chemistry and Biochemistry, 2017, University of Notre Dame

  People need high quality fortified foods and medicines to protect their health. However, bad quality products are on the market. Regulatory agencies can remove… (more)

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APA (6th Edition):

Myers, N. M. (2017). Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/6395w66579v

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Myers, Nicholas M.. “Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>.” 2017. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/6395w66579v.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Myers, Nicholas M.. “Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>.” 2017. Web. 13 Aug 2020.

Vancouver:

Myers NM. Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>. [Internet] [Thesis]. University of Notre Dame; 2017. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/6395w66579v.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Myers NM. Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>. [Thesis]. University of Notre Dame; 2017. Available from: https://curate.nd.edu/show/6395w66579v

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

4. Timothy Adam Wencewicz. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.

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

  Anitibiotic resistance is developing at an alarming rate and is one of the world’s most pressing health problems. New methods for developing microbe-selective antibacterial… (more)

Subjects/Keywords: sideromycin; hydroxylamine; antibiotic delivery; salmycin; albomycin; drug delivery; structure-activity relationship; siderophore; active transport; diversity-oriented synthesis; microcin; nitroso; hydroxamic acid

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APA (6th Edition):

Wencewicz, T. A. (2011). Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/5m60qr48p6n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/5m60qr48p6n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Web. 13 Aug 2020.

Vancouver:

Wencewicz TA. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. [Internet] [Thesis]. University of Notre Dame; 2011. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/5m60qr48p6n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wencewicz TA. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. [Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/5m60qr48p6n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

5. Andrew David Kosal. New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>.

Degree: Chemistry and Biochemistry, 2013, University of Notre Dame

  A method utilizing catalytic titanocene dichloride for the conjugate reduction of α,β-unsaturated carbonyls was developed and described herein. The chemoselective procedure employs an amine… (more)

Subjects/Keywords: Staudinger; titanium; amide; phosphorus; reduction; carbonyl

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APA (6th Edition):

Kosal, A. D. (2013). New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/ns064457m3b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kosal, Andrew David. “New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>.” 2013. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/ns064457m3b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kosal, Andrew David. “New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>.” 2013. Web. 13 Aug 2020.

Vancouver:

Kosal AD. New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>. [Internet] [Thesis]. University of Notre Dame; 2013. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/ns064457m3b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kosal AD. New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>. [Thesis]. University of Notre Dame; 2013. Available from: https://curate.nd.edu/show/ns064457m3b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

6. Raúl Erick Juá‡rez Hernández. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.

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

  Siderophores are extremely versatile molecules synthesized by a variety of organisms with the objective of gathering iron, an essential element for most of living… (more)

Subjects/Keywords: desferrioxamine B; drug-conjugate; mycobactin; siderophore; sideromycin

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APA (6th Edition):

Hernández, R. E. J. (2012). A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/ft848p60v7m

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hernández, Raúl Erick Juá‡rez. “A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.” 2012. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/ft848p60v7m.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hernández, Raúl Erick Juá‡rez. “A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.” 2012. Web. 13 Aug 2020.

Vancouver:

Hernández REJ. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. [Internet] [Thesis]. University of Notre Dame; 2012. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/ft848p60v7m.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hernández REJ. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. [Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/ft848p60v7m

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

7. Erin Wilson. Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>.

Degree: Chemistry and Biochemistry, 2015, University of Notre Dame

  New methods for the phosphorus-mediated activation of C–O, N–O, C=O, and C–X bonds are reported herein. The first of which is a Staudinger ligation… (more)

Subjects/Keywords: catalysis; phosphorus; amidines; amides

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APA (6th Edition):

Wilson, E. (2015). Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/bg257d29b2n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wilson, Erin. “Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>.” 2015. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/bg257d29b2n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wilson, Erin. “Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>.” 2015. Web. 13 Aug 2020.

Vancouver:

Wilson E. Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>. [Internet] [Thesis]. University of Notre Dame; 2015. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/bg257d29b2n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wilson E. Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>. [Thesis]. University of Notre Dame; 2015. Available from: https://curate.nd.edu/show/bg257d29b2n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

8. 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: 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>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b01f5m

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/0k225b01f5m.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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. 13 Aug 2020.

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] [Thesis]. University of Notre Dame; 2012. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/0k225b01f5m.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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>. [Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/0k225b01f5m

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

9. Jeremy A Bates. Efforts toward the Total Synthesis of Sphinxolide</h1>.

Degree: Chemistry and Biochemistry, 2006, University of Notre Dame

  This thesis discusses the efforts toward the total synthesis of sphinxolide; specifically, it focuses on the synthesis of the Joint, East, and South fragments… (more)

Subjects/Keywords: sphinxolide

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APA (6th Edition):

Bates, J. A. (2006). Efforts toward the Total Synthesis of Sphinxolide</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/g445cc10q76

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bates, Jeremy A. “Efforts toward the Total Synthesis of Sphinxolide</h1>.” 2006. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/g445cc10q76.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bates, Jeremy A. “Efforts toward the Total Synthesis of Sphinxolide</h1>.” 2006. Web. 13 Aug 2020.

Vancouver:

Bates JA. Efforts toward the Total Synthesis of Sphinxolide</h1>. [Internet] [Thesis]. University of Notre Dame; 2006. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/g445cc10q76.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bates JA. Efforts toward the Total Synthesis of Sphinxolide</h1>. [Thesis]. University of Notre Dame; 2006. Available from: https://curate.nd.edu/show/g445cc10q76

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

10. Jeremiah J. Gassensmith. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.

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

  Squaraine dyes are a unique class of near-infrared fluorophores that have fascinated researchers because of their interesting donor-acceptor structure and their electron deficient aromatic… (more)

Subjects/Keywords: Squaraine; Dyes; Chemistry; Supramolecular; Macrocycles; Probes; Anthracene

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APA (6th Edition):

Gassensmith, J. J. (2009). The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/jq085h75x57

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/jq085h75x57.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Web. 13 Aug 2020.

Vancouver:

Gassensmith JJ. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. [Internet] [Thesis]. University of Notre Dame; 2009. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/jq085h75x57.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gassensmith JJ. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. [Thesis]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/jq085h75x57

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

11. Coura Rosalie Diène. Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>.

Degree: Chemistry and Biochemistry, 2007, University of Notre Dame

  The ambruticins are a class of polyketide natural products that were isolated in 1977 which have been shown to be completely non-toxic with low… (more)

Subjects/Keywords: synthesis; hydropyran; cyclopropanation; Julia

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APA (6th Edition):

Diène, C. R. (2007). Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/c247dr2919w

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Diène, Coura Rosalie. “Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>.” 2007. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/c247dr2919w.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Diène, Coura Rosalie. “Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>.” 2007. Web. 13 Aug 2020.

Vancouver:

Diène CR. Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>. [Internet] [Thesis]. University of Notre Dame; 2007. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/c247dr2919w.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Diène CR. Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>. [Thesis]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/c247dr2919w

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

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

Degree: 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>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/n583xs57z1t

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/n583xs57z1t.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Web. 13 Aug 2020.

Vancouver:

Chormanski K. Alkyne Substituent Effects in Radicals and Carbocations</h1>. [Internet] [Thesis]. University of Notre Dame; 2010. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/n583xs57z1t.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

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

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

13. James Chenkuo Tung. Towards the synthesis of the cornexistins</h1>.

Degree: Chemistry and Biochemistry, 2007, University of Notre Dame

  Cornexistin and hydroxycornexistin are natural products derived from the fungus Paecilomyces variotti. Both cornexistin and hydroxycornexistin are highly potent herbicides that have the unique… (more)

Subjects/Keywords: cornexistin; nine membered ring; ring closing

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APA (6th Edition):

Tung, J. C. (2007). Towards the synthesis of the cornexistins</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/7h149p3103n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tung, James Chenkuo. “Towards the synthesis of the cornexistins</h1>.” 2007. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/7h149p3103n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tung, James Chenkuo. “Towards the synthesis of the cornexistins</h1>.” 2007. Web. 13 Aug 2020.

Vancouver:

Tung JC. Towards the synthesis of the cornexistins</h1>. [Internet] [Thesis]. University of Notre Dame; 2007. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/7h149p3103n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tung JC. Towards the synthesis of the cornexistins</h1>. [Thesis]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/7h149p3103n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

14. Katherine Waring. Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>.

Degree: Chemistry and Biochemistry, 2007, University of Notre Dame

Subjects/Keywords: 2; retro Diels-Alder reaction; piperine; ergosterol; 5-dihydropyrrole; hetero-Diels-Alder

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APA (6th Edition):

Waring, K. (2007). Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/b5644q79j2q

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Waring, Katherine. “Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>.” 2007. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/b5644q79j2q.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Waring, Katherine. “Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>.” 2007. Web. 13 Aug 2020.

Vancouver:

Waring K. Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>. [Internet] [Thesis]. University of Notre Dame; 2007. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/b5644q79j2q.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Waring K. Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>. [Thesis]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/b5644q79j2q

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

15. Lawrence P. Tardibono Jr. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.

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

  New methodologies were developed and used to synthesize novel benzodiazepines with anti-cancer activity and carbocyclic nucleosides. Appropriately functionalized acylnitroso-derived hetero-Diels-Alder cycloadducts were subjected to… (more)

Subjects/Keywords: organic synthesis; benzodiazepines; palladium allylation; nucleosides; nitroso; decarboxylation

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APA (6th Edition):

Jr., L. P. T. (2010). Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/h128nc60644

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jr., Lawrence P. Tardibono. “Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.” 2010. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/h128nc60644.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jr., Lawrence P. Tardibono. “Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.” 2010. Web. 13 Aug 2020.

Vancouver:

Jr. LPT. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. [Internet] [Thesis]. University of Notre Dame; 2010. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/h128nc60644.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jr. LPT. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. [Thesis]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/h128nc60644

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Notre Dame

16. Joshua Kyle Bolger. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.

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

  Acylnitroso cycloadducts have proven to be valuable intermediates in the syntheses of a plethora of biologically active molecules. The utility of relatively simple intermediates… (more)

Subjects/Keywords: acylnitroso cycloaddition; lipoxygenase inhibitors; regioselective ring-opening

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APA (6th Edition):

Bolger, J. K. (2009). Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/7p88cf97h8n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bolger, Joshua Kyle. “Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.” 2009. Thesis, University of Notre Dame. Accessed August 13, 2020. https://curate.nd.edu/show/7p88cf97h8n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bolger, Joshua Kyle. “Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.” 2009. Web. 13 Aug 2020.

Vancouver:

Bolger JK. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. [Internet] [Thesis]. University of Notre Dame; 2009. [cited 2020 Aug 13]. Available from: https://curate.nd.edu/show/7p88cf97h8n.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bolger JK. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. [Thesis]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/7p88cf97h8n

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.