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You searched for +publisher:"Dalhousie University" +contributor:("Robert L. White"). Showing records 1 – 5 of 5 total matches.

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Dalhousie University

1. Saunders, Cheryl D.L. Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase.

Degree: PhD, Department of Chemistry, 2009, Dalhousie University

 Although some physiological effects of toxic metal poisoning have been known for centuries, the specific chemical interactions between biological molecules and mercury(I), mercury(II) or lead(II)… (more)

Subjects/Keywords: chemistry; lead; mercury; amino acids; ESI-MS; NMR; X-ray crystallography

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APA (6th Edition):

Saunders, C. D. L. (2009). Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/12228

Chicago Manual of Style (16th Edition):

Saunders, Cheryl D L. “Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase.” 2009. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/12228.

MLA Handbook (7th Edition):

Saunders, Cheryl D L. “Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase.” 2009. Web. 29 May 2020.

Vancouver:

Saunders CDL. Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase. [Internet] [Doctoral dissertation]. Dalhousie University; 2009. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/12228.

Council of Science Editors:

Saunders CDL. Isolation of Lead-Amino Acid and Mercury-Amino Acid Complexes with Characterization in the Solid State, the Solution State, and the Gas Phase. [Doctoral Dissertation]. Dalhousie University; 2009. Available from: http://hdl.handle.net/10222/12228


Dalhousie University

2. Wall, Mark James. Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery.

Degree: PhD, Department of Chemistry, 2010, Dalhousie University

 Two popular workflows exist for quantitative proteome analysis: two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), with staining to visualize proteins, and multidimensional solution phase separations of isotopically… (more)

Subjects/Keywords: Proteomics; Mass spectrometry; Biomarkers; Matrix-assisted laser desorption/ionization; Electrospray ionization

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APA (6th Edition):

Wall, M. J. (2010). Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/12840

Chicago Manual of Style (16th Edition):

Wall, Mark James. “Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery.” 2010. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/12840.

MLA Handbook (7th Edition):

Wall, Mark James. “Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery.” 2010. Web. 29 May 2020.

Vancouver:

Wall MJ. Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery. [Internet] [Doctoral dissertation]. Dalhousie University; 2010. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/12840.

Council of Science Editors:

Wall MJ. Towards the Development of a Proteomics Workflow for High-throughput Protein Biomarker Discovery. [Doctoral Dissertation]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/12840


Dalhousie University

3. Tovstiga, Tara. Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions.

Degree: MS, Department of Chemistry, 2013, Dalhousie University

 A library of 2-nitrobenzenesulfonyl (Ns) derivatives incorporating isotopic labels and a range of structural variations was prepared and characterized to investigate mass spectrometric fragmentation processes.… (more)

Subjects/Keywords: Chemistry; mass spectrometry; negative ion

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APA (6th Edition):

Tovstiga, T. (2013). Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/35370

Chicago Manual of Style (16th Edition):

Tovstiga, Tara. “Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions.” 2013. Masters Thesis, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/35370.

MLA Handbook (7th Edition):

Tovstiga, Tara. “Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions.” 2013. Web. 29 May 2020.

Vancouver:

Tovstiga T. Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/35370.

Council of Science Editors:

Tovstiga T. Novel Fragmentation Processes of 2-Nitrobenzenesulfonyl Amino Acid Anions. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/35370


Dalhousie University

4. Moulins, Jonathan. Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes.

Degree: PhD, Department of Chemistry, 2013, Dalhousie University

 Heterocycles were prepared through the geminal acylation of 2-methoxyoxazolidines with 1,2-bis(trimethylsilyloxy)cyclobutene. It was found that when water was excluded from the standard reaction conditions, regioselectivity… (more)

Subjects/Keywords: Organic; Synthesis; Methodology

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APA (6th Edition):

Moulins, J. (2013). Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/37454

Chicago Manual of Style (16th Edition):

Moulins, Jonathan. “Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes.” 2013. Doctoral Dissertation, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/37454.

MLA Handbook (7th Edition):

Moulins, Jonathan. “Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes.” 2013. Web. 29 May 2020.

Vancouver:

Moulins J. Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/37454.

Council of Science Editors:

Moulins J. Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/37454

5. Ruzic-Gauthier, Michael. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.

Degree: MS, Department of Chemistry, 2013, Dalhousie University

 DNA photocleaving reagents are a unique class of molecules that display the ability to cleave DNA, causing strand breaks, upon exposure to an irradiation source.… (more)

Subjects/Keywords: two-photon excitation; DNA cleavage

…my supervisory committee members Dr. Frances L. Cozens and Dr. Robert L. White. Aside from… 

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

APA (6th Edition):

Ruzic-Gauthier, M. (2013). Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/36323

Chicago Manual of Style (16th Edition):

Ruzic-Gauthier, Michael. “Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.” 2013. Masters Thesis, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/36323.

MLA Handbook (7th Edition):

Ruzic-Gauthier, Michael. “Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones.” 2013. Web. 29 May 2020.

Vancouver:

Ruzic-Gauthier M. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/36323.

Council of Science Editors:

Ruzic-Gauthier M. Cleavage of duplex DNA using two-photon excitation of N-(alkoxy)pyridine thiones. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/36323

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