Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

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

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/jq085h75x57.

MLA Handbook (7th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Web. 26 Jun 2019.

Vancouver:

Gassensmith JJ. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/jq085h75x57.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Myers, Nicholas M.. “Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>.” 2017. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/6395w66579v.

MLA Handbook (7th Edition):

Myers, Nicholas M.. “Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>.” 2017. Web. 26 Jun 2019.

Vancouver:

Myers NM. Lab on Paper: Adapting Quantitative Chemical Techniques for Use in Low Resource Areas</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2017. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/6395w66579v.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Kosal, Andrew David. “New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>.” 2013. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/ns064457m3b.

MLA Handbook (7th Edition):

Kosal, Andrew David. “New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>.” 2013. Web. 26 Jun 2019.

Vancouver:

Kosal AD. New Discoveries in Titanium and Phosphorus Mediated Carbonyl Additions</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2013. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/ns064457m3b.

Council of Science Editors:

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


University of Notre Dame

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/5m60qr48p6n.

MLA Handbook (7th Edition):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Web. 26 Jun 2019.

Vancouver:

Wencewicz TA. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2011. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/5m60qr48p6n.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Clear, Kasey J. “Molecular Probes for Biomembrane Recognition</h1>.” 2016. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/dv13zs2842v.

MLA Handbook (7th Edition):

Clear, Kasey J. “Molecular Probes for Biomembrane Recognition</h1>.” 2016. Web. 26 Jun 2019.

Vancouver:

Clear KJ. Molecular Probes for Biomembrane Recognition</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2016. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/dv13zs2842v.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Gianino, Joseph Bartholomew. “Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>.” 2014. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/fj236111169.

MLA Handbook (7th Edition):

Gianino, Joseph Bartholomew. “Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>.” 2014. Web. 26 Jun 2019.

Vancouver:

Gianino JB. Development of Titanocene-Catalyzed Multicomponent Coupling Reactions</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2014. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/fj236111169.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/7p88cf97h8n.

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. 26 Jun 2019.

Vancouver:

Bolger JK. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/7p88cf97h8n.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Wilson, Erin. “Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>.” 2015. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/bg257d29b2n.

MLA Handbook (7th Edition):

Wilson, Erin. “Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>.” 2015. Web. 26 Jun 2019.

Vancouver:

Wilson E. Phosphorus Mediated Reactions Toward the Advancement of C-N and C-C Bond Formations</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2015. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/bg257d29b2n.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/h128nc60644

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. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/h128nc60644.

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. 26 Jun 2019.

Vancouver:

Jr. LPT. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2010. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/h128nc60644.

Council of Science Editors:

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


University of Notre Dame

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/ft848p60v7m.

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. 26 Jun 2019.

Vancouver:

Hernández REJ. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/ft848p60v7m.

Council of Science Editors:

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


University of Notre Dame

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

Degree: MS, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Bates, Jeremy A. “Efforts toward the Total Synthesis of Sphinxolide</h1>.” 2006. Masters Thesis, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/g445cc10q76.

MLA Handbook (7th Edition):

Bates, Jeremy A. “Efforts toward the Total Synthesis of Sphinxolide</h1>.” 2006. Web. 26 Jun 2019.

Vancouver:

Bates JA. Efforts toward the Total Synthesis of Sphinxolide</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2006. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/g445cc10q76.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Diène, Coura Rosalie. “Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>.” 2007. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/c247dr2919w.

MLA Handbook (7th Edition):

Diène, Coura Rosalie. “Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>.” 2007. Web. 26 Jun 2019.

Vancouver:

Diène CR. Progress towards the Syntheses of Ambruticin and Its Putative Biosynthetic Intermediate</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/c247dr2919w.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Tung, James Chenkuo. “Towards the synthesis of the cornexistins</h1>.” 2007. Doctoral Dissertation, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/7h149p3103n.

MLA Handbook (7th Edition):

Tung, James Chenkuo. “Towards the synthesis of the cornexistins</h1>.” 2007. Web. 26 Jun 2019.

Vancouver:

Tung JC. Towards the synthesis of the cornexistins</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/7h149p3103n.

Council of Science Editors:

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


University of Notre Dame

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

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Waring, Katherine. “Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>.” 2007. Masters Thesis, University of Notre Dame. Accessed June 26, 2019. https://curate.nd.edu/show/b5644q79j2q.

MLA Handbook (7th Edition):

Waring, Katherine. “Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>.” 2007. Web. 26 Jun 2019.

Vancouver:

Waring K. Natural Product Derivatization Through Nitroso Diels-Alder Reactions</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2007. [cited 2019 Jun 26]. Available from: https://curate.nd.edu/show/b5644q79j2q.

Council of Science Editors:

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

.