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You searched for +publisher:"Dalhousie University" +contributor:("Frances L. Cozens"). Showing records 1 – 4 of 4 total matches.

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Dalhousie University

1. Martinez-Farina, Camilo. Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins.

Degree: MS, Department of Chemistry, 2015, Dalhousie University

 Nature produces many clinically used medicines in the form of natural products. These compounds can be isolated from a variety of sources, but bacteria have… (more)

Subjects/Keywords: Natural Products; Jadomycin; Precursor-Directed Biosynthesis; WaterLOGSY

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APA (6th Edition):

Martinez-Farina, C. (2015). Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/56323

Chicago Manual of Style (16th Edition):

Martinez-Farina, Camilo. “Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins.” 2015. Masters Thesis, Dalhousie University. Accessed May 29, 2020. http://hdl.handle.net/10222/56323.

MLA Handbook (7th Edition):

Martinez-Farina, Camilo. “Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins.” 2015. Web. 29 May 2020.

Vancouver:

Martinez-Farina C. Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins. [Internet] [Masters thesis]. Dalhousie University; 2015. [cited 2020 May 29]. Available from: http://hdl.handle.net/10222/56323.

Council of Science Editors:

Martinez-Farina C. Investigations into the Biosynthesis, Derivatization, and Purification of Jadomycins. [Masters Thesis]. Dalhousie University; 2015. Available from: http://hdl.handle.net/10222/56323


Dalhousie University

2. 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

3. 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


Dalhousie University

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

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

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