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 subject:(Organic synthesis). Showing records 1 – 30 of 2230 total matches.

[1] [2] [3] [4] [5] … [75]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


Dalhousie University

1. Aish, Gaia Ashlee. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates.

Degree: MS, Department of Chemistry, 2014, Dalhousie University

 Phosphonates are commonly used as hydrolytically stable phosphate mimics to explore a multitude of biological processes. This general approach has lead to the development of… (more)

Subjects/Keywords: organic synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Aish, G. A. (2014). The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/54086

Chicago Manual of Style (16th Edition):

Aish, Gaia Ashlee. “The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates.” 2014. Masters Thesis, Dalhousie University. Accessed April 03, 2020. http://hdl.handle.net/10222/54086.

MLA Handbook (7th Edition):

Aish, Gaia Ashlee. “The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates.” 2014. Web. 03 Apr 2020.

Vancouver:

Aish GA. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10222/54086.

Council of Science Editors:

Aish GA. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. [Masters Thesis]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/54086


Brock University

2. Gilmet, Jacqueline. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .

Degree: Department of Chemistry, 2010, Brock University

 The present thesis reviews the development of a formal enantiodivergent synthesis of the (+)- and (-)-isomers of balanol. This approach commences from a cis-dihydrodiol derived… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Codeine  – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gilmet, J. (2010). Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3033

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):

Gilmet, Jacqueline. “Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .” 2010. Thesis, Brock University. Accessed April 03, 2020. http://hdl.handle.net/10464/3033.

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

MLA Handbook (7th Edition):

Gilmet, Jacqueline. “Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .” 2010. Web. 03 Apr 2020.

Vancouver:

Gilmet J. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . [Internet] [Thesis]. Brock University; 2010. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10464/3033.

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

Council of Science Editors:

Gilmet J. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . [Thesis]. Brock University; 2010. Available from: http://hdl.handle.net/10464/3033

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


Brock University

3. Metcalf, Thomas A. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .

Degree: Department of Chemistry, 2011, Brock University

 The present studies describe our recent work on expanding the use of the Burgess reagent and its reaction with oxiranes. Several new variants of the… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Morphine  – Synthesis.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Metcalf, T. A. (2011). Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3417

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):

Metcalf, Thomas A. “Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .” 2011. Thesis, Brock University. Accessed April 03, 2020. http://hdl.handle.net/10464/3417.

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

MLA Handbook (7th Edition):

Metcalf, Thomas A. “Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .” 2011. Web. 03 Apr 2020.

Vancouver:

Metcalf TA. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . [Internet] [Thesis]. Brock University; 2011. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10464/3417.

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

Council of Science Editors:

Metcalf TA. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . [Thesis]. Brock University; 2011. Available from: http://hdl.handle.net/10464/3417

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


Nelson Mandela Metropolitan University

4. Mahanjana, Lungelwa. Reactions towards the synthesis of the uncommon P57 cymarose moiety.

Degree: Faculty of Science, 2013, Nelson Mandela Metropolitan University

 The work described in this study aims to investigate methods that will improve a lengthy synthetic pathway in the synthesis of the P57 cymarose moiety,… (more)

Subjects/Keywords: Chemistry, Organic; Organic compounds  – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mahanjana, L. (2013). Reactions towards the synthesis of the uncommon P57 cymarose moiety. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/6711

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):

Mahanjana, Lungelwa. “Reactions towards the synthesis of the uncommon P57 cymarose moiety.” 2013. Thesis, Nelson Mandela Metropolitan University. Accessed April 03, 2020. http://hdl.handle.net/10948/6711.

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

MLA Handbook (7th Edition):

Mahanjana, Lungelwa. “Reactions towards the synthesis of the uncommon P57 cymarose moiety.” 2013. Web. 03 Apr 2020.

Vancouver:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2013. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10948/6711.

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

Council of Science Editors:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Thesis]. Nelson Mandela Metropolitan University; 2013. Available from: http://hdl.handle.net/10948/6711

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


University of Colorado

5. Nedungadi, Sachin. Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission.

Degree: MS, Chemistry & Biochemistry, 2016, University of Colorado

  The present work is directed toward the synthesis of small chromophores capable of exhibiting singlet fission which can be utilized for application in solar… (more)

Subjects/Keywords: Physical Organic; Synthesis; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nedungadi, S. (2016). Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/191

Chicago Manual of Style (16th Edition):

Nedungadi, Sachin. “Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission.” 2016. Masters Thesis, University of Colorado. Accessed April 03, 2020. https://scholar.colorado.edu/chem_gradetds/191.

MLA Handbook (7th Edition):

Nedungadi, Sachin. “Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission.” 2016. Web. 03 Apr 2020.

Vancouver:

Nedungadi S. Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission. [Internet] [Masters thesis]. University of Colorado; 2016. [cited 2020 Apr 03]. Available from: https://scholar.colorado.edu/chem_gradetds/191.

Council of Science Editors:

Nedungadi S. Starting Materials for the Synthesis of Biradicaloid Heterocycles as Small Chromophores for Singlet Fission. [Masters Thesis]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/chem_gradetds/191


University of Oxford

6. Akhtar, Wasim. The α-alkylation of ketones using hydrogen borrowing catalysis.

Degree: PhD, 2018, University of Oxford

 <b>Introduction - Hydrogen Borrowing Alkylation Reactions Using Alcohols</b> The introduction reviews the origins of hydrogen borrowing catalysis and how it has been applied to utilise… (more)

Subjects/Keywords: Organic Chemistry; Organic compounds – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Akhtar, W. (2018). The α-alkylation of ketones using hydrogen borrowing catalysis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421

Chicago Manual of Style (16th Edition):

Akhtar, Wasim. “The α-alkylation of ketones using hydrogen borrowing catalysis.” 2018. Doctoral Dissertation, University of Oxford. Accessed April 03, 2020. http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421.

MLA Handbook (7th Edition):

Akhtar, Wasim. “The α-alkylation of ketones using hydrogen borrowing catalysis.” 2018. Web. 03 Apr 2020.

Vancouver:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Apr 03]. Available from: http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421.

Council of Science Editors:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421


Rutgers University

7. Ramanathan, Ahalya. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.

Degree: PhD, Chemistry and Chemical Biology, 2011, Rutgers University

TMC-95A is a natural product which has demonstrated inhibition activity against the proteasomal pathway. Though its biological activity is proven, the total synthesis of the… (more)

Subjects/Keywords: Chemistry, Organic; Organic compounds – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramanathan, A. (2011). I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673

Chicago Manual of Style (16th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Doctoral Dissertation, Rutgers University. Accessed April 03, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

MLA Handbook (7th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Web. 03 Apr 2020.

Vancouver:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2020 Apr 03]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

Council of Science Editors:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673


Dalhousie University

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 April 03, 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. 03 Apr 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 Apr 03]. 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


University of Hawaii

9. Ebisu, Kikuye. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography: leaves [60]-64.

x, 64 l illus

The highly strained bicyclo[2.1.1]hexane system has been of considerable interest to chemists especially in connection with bond… (more)

Subjects/Keywords: Organic compounds  – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ebisu, K. (2009). The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11389

Chicago Manual of Style (16th Edition):

Ebisu, Kikuye. “The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.” 2009. Doctoral Dissertation, University of Hawaii. Accessed April 03, 2020. http://hdl.handle.net/10125/11389.

MLA Handbook (7th Edition):

Ebisu, Kikuye. “The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.” 2009. Web. 03 Apr 2020.

Vancouver:

Ebisu K. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10125/11389.

Council of Science Editors:

Ebisu K. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11389


University of Hong Kong

10. He, Jiayun. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.

Degree: PhD, 2017, University of Hong Kong

The intramolecular (4+3) cycloadditions of epoxy enolsilane substrates 1.89 generated polycyclic cycloadducts 1.90 having bicyclo[5.3.0]decane frameworks, a skeleton which is common among terpenoid natural products… (more)

Subjects/Keywords: Organic compounds - Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

He, J. (2017). Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/241419

Chicago Manual of Style (16th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. http://hdl.handle.net/10722/241419.

MLA Handbook (7th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Web. 03 Apr 2020.

Vancouver:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Internet] [Doctoral dissertation]. University of Hong Kong; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10722/241419.

Council of Science Editors:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Doctoral Dissertation]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/241419


University of Manitoba

11. Othen, Edwin. The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues.

Degree: Chemistry, 2017, University of Manitoba

 I would like to convey my sincerest thanks to my supervisor Dr. John Sorensen for his seemingly unending patience and compassion; without it I would… (more)

Subjects/Keywords: Chemistry; Organic Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Othen, E. (2017). The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32766

Chicago Manual of Style (16th Edition):

Othen, Edwin. “The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues.” 2017. Masters Thesis, University of Manitoba. Accessed April 03, 2020. http://hdl.handle.net/1993/32766.

MLA Handbook (7th Edition):

Othen, Edwin. “The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues.” 2017. Web. 03 Apr 2020.

Vancouver:

Othen E. The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues. [Internet] [Masters thesis]. University of Manitoba; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1993/32766.

Council of Science Editors:

Othen E. The synthesis of novel fuels from polyhydroxyalkanoates and g-quadruplex stabilizers as well as their analogues. [Masters Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32766


Boston University

12. Wong, Christopher Ryan. Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes.

Degree: PhD, Chemistry, 2019, Boston University

 The unique ability of allyl and crotyl silane reagents to act as competent nucleophiles as well as electron-rich dienophiles prompted an investigation into utilizing allyl… (more)

Subjects/Keywords: Chemistry; Organic synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wong, C. R. (2019). Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/39378

Chicago Manual of Style (16th Edition):

Wong, Christopher Ryan. “Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes.” 2019. Doctoral Dissertation, Boston University. Accessed April 03, 2020. http://hdl.handle.net/2144/39378.

MLA Handbook (7th Edition):

Wong, Christopher Ryan. “Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes.” 2019. Web. 03 Apr 2020.

Vancouver:

Wong CR. Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes. [Internet] [Doctoral dissertation]. Boston University; 2019. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/2144/39378.

Council of Science Editors:

Wong CR. Enantioselective reactions of crotyl silane with ortho-quinone methide intermediates and progress toward an asymmetric cyclopropanation of allenylsilanes. [Doctoral Dissertation]. Boston University; 2019. Available from: http://hdl.handle.net/2144/39378


Georgia Tech

13. Mojica, Mike. Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures.

Degree: PhD, Chemistry and Biochemistry, 2014, Georgia Tech

 This thesis explores three rare synthetic routes: the synthesis of hydrazines via the aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions… (more)

Subjects/Keywords: Organic chemistry; Hydrazine Synthesis; Azides Synthesis; Organic compounds Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mojica, M. (2014). Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51791

Chicago Manual of Style (16th Edition):

Mojica, Mike. “Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 03, 2020. http://hdl.handle.net/1853/51791.

MLA Handbook (7th Edition):

Mojica, Mike. “Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures.” 2014. Web. 03 Apr 2020.

Vancouver:

Mojica M. Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1853/51791.

Council of Science Editors:

Mojica M. Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/51791


Iowa State University

14. Hale, Benjamin James. Influence of heterocycle substitution in π-functional materials for organic photovoltaics.

Degree: 2015, Iowa State University

 Heterocycle substitution can have a dramatic, and potentially unintended, impact the physical, optical, electrochemical, and photovoltaic properties of donor materials used in organic electronics. A… (more)

Subjects/Keywords: Organic Chemistry; Organic electronics; Organic photovoltaics; Organic synthesis; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hale, B. J. (2015). Influence of heterocycle substitution in π-functional materials for organic photovoltaics. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14833

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):

Hale, Benjamin James. “Influence of heterocycle substitution in π-functional materials for organic photovoltaics.” 2015. Thesis, Iowa State University. Accessed April 03, 2020. https://lib.dr.iastate.edu/etd/14833.

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

MLA Handbook (7th Edition):

Hale, Benjamin James. “Influence of heterocycle substitution in π-functional materials for organic photovoltaics.” 2015. Web. 03 Apr 2020.

Vancouver:

Hale BJ. Influence of heterocycle substitution in π-functional materials for organic photovoltaics. [Internet] [Thesis]. Iowa State University; 2015. [cited 2020 Apr 03]. Available from: https://lib.dr.iastate.edu/etd/14833.

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

Council of Science Editors:

Hale BJ. Influence of heterocycle substitution in π-functional materials for organic photovoltaics. [Thesis]. Iowa State University; 2015. Available from: https://lib.dr.iastate.edu/etd/14833

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


University of Hong Kong

15. Ou, Jun. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.

Degree: PhD, 2011, University of Hong Kong

 Two syntheses of non-cross-linked polystyrene-supported TADDOL-based phosphoric acid organocatalyst have been developed. The optimal polymer-supported catalyst 2.29d exhibited comparable catalytic activity to its small molecule… (more)

Subjects/Keywords: Asymmetric synthesis.; Catalysis.; Organic compounds - Synthesis.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ou, J. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528

Chicago Manual of Style (16th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

MLA Handbook (7th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Web. 03 Apr 2020.

Vancouver:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2020 Apr 03]. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

Council of Science Editors:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528


University of Hawaii – Manoa

16. Zou, Xianglong. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.

Degree: PhD, 2009, University of Hawaii – Manoa

Microfiche.

xi, 127 leaves, bound ill. 29 cm

Part I: The stereoselective total synthesis of each of the two diastereomeric C6-hydroxyhexahydrocannabinols is described. The extension… (more)

Subjects/Keywords: Cannabinoids  – Synthesis; Sarcophyton; Organic compounds  – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zou, X. (2009). Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9527

Chicago Manual of Style (16th Edition):

Zou, Xianglong. “Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed April 03, 2020. http://hdl.handle.net/10125/9527.

MLA Handbook (7th Edition):

Zou, Xianglong. “Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.” 2009. Web. 03 Apr 2020.

Vancouver:

Zou X. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10125/9527.

Council of Science Editors:

Zou X. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9527


University of Hong Kong

17. Hermeke, Julia. Chiral phosphonium ion tagged and spiroindane-based organocatalysts.

Degree: M. Phil., 2011, University of Hong Kong

The research on asymmetric organocatalysis has been intensifying since the beginning of 2000. The growing interest in this research area is driven by the importance… (more)

Subjects/Keywords: Organic compounds - Synthesis; Asymmetric synthesis; Catalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hermeke, J. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Masters Thesis). University of Hong Kong. Retrieved from Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871

Chicago Manual of Style (16th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Masters Thesis, University of Hong Kong. Accessed April 03, 2020. Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

MLA Handbook (7th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Web. 03 Apr 2020.

Vancouver:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2020 Apr 03]. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

Council of Science Editors:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Masters Thesis]. University of Hong Kong; 2011. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871


University of Hong Kong

18. 汪子玉; Wang, Ziyu. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.

Degree: PhD, 2012, University of Hong Kong

The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream of organic chemists. In the past decades, organocatalysis has been… (more)

Subjects/Keywords: Nitroalkenes; Asymmetric synthesis; Dibenzofurans; Organic compounds - Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

汪子玉; Wang, Z. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388

Chicago Manual of Style (16th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

MLA Handbook (7th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Web. 03 Apr 2020.

Vancouver:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Apr 03]. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

Council of Science Editors:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388


Brock University

19. Xu, Shufen. Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts .

Degree: Centre for Biotechnology, 2010, Brock University

 Compounds containing the pyrrolidine moiety are key substructures of compounds with biological activity and organocatalysts. In particular, annulated chiral pyrrolidines with alpha stereogenic centers have… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Aldosterone  – Synthesis; Pyrrolidine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xu, S. (2010). Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3043

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):

Xu, Shufen. “Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts .” 2010. Thesis, Brock University. Accessed April 03, 2020. http://hdl.handle.net/10464/3043.

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

MLA Handbook (7th Edition):

Xu, Shufen. “Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts .” 2010. Web. 03 Apr 2020.

Vancouver:

Xu S. Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts . [Internet] [Thesis]. Brock University; 2010. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10464/3043.

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

Council of Science Editors:

Xu S. Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones. Access to aldosterone synthase inhibitors and chiral precatalysts . [Thesis]. Brock University; 2010. Available from: http://hdl.handle.net/10464/3043

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


University of Adelaide

20. Pepper, Henry Patrick. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.

Degree: 2016, University of Adelaide

 Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation were undertaken in order to gain biosynthetic insight and to develop efficient syntheses of… (more)

Subjects/Keywords: chemistry; organic; biomimetic synthesis; natural product synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pepper, H. P. (2016). Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/114063

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):

Pepper, Henry Patrick. “Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.” 2016. Thesis, University of Adelaide. Accessed April 03, 2020. http://hdl.handle.net/2440/114063.

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

MLA Handbook (7th Edition):

Pepper, Henry Patrick. “Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.” 2016. Web. 03 Apr 2020.

Vancouver:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/2440/114063.

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

Council of Science Editors:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/114063

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

21. Chen, Joanna. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.

Degree: 2017, University of California – eScholarship, University of California

 Cyanobacteria, also known as blue-green algae, are prokaryotic organisms that inhabit freshwater and brackish lakes. They produce toxic secondary metabolites known as cyanotoxins, the increased… (more)

Subjects/Keywords: Organic chemistry; natural product synthesis; total synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, J. (2017). Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/5m39680q

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):

Chen, Joanna. “Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.” 2017. Thesis, University of California – eScholarship, University of California. Accessed April 03, 2020. http://www.escholarship.org/uc/item/5m39680q.

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

MLA Handbook (7th Edition):

Chen, Joanna. “Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.” 2017. Web. 03 Apr 2020.

Vancouver:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Internet] [Thesis]. University of California – eScholarship, University of California; 2017. [cited 2020 Apr 03]. Available from: http://www.escholarship.org/uc/item/5m39680q.

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

Council of Science Editors:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Thesis]. University of California – eScholarship, University of California; 2017. Available from: http://www.escholarship.org/uc/item/5m39680q

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

22. Herrmann, Aaron Thomas. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.

Degree: 2015, University of California – eScholarship, University of California

 Marine natural products have long served as promising compounds and scaffolds for new therapeutic agents; however, their utilization is often extremely limited due to poor… (more)

Subjects/Keywords: Chemistry; Chemistry; Methodology; Organic; Synthesis; Total Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Herrmann, A. T. (2015). Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/8fd8138z

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):

Herrmann, Aaron Thomas. “Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.” 2015. Thesis, University of California – eScholarship, University of California. Accessed April 03, 2020. http://www.escholarship.org/uc/item/8fd8138z.

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

MLA Handbook (7th Edition):

Herrmann, Aaron Thomas. “Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.” 2015. Web. 03 Apr 2020.

Vancouver:

Herrmann AT. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. [Internet] [Thesis]. University of California – eScholarship, University of California; 2015. [cited 2020 Apr 03]. Available from: http://www.escholarship.org/uc/item/8fd8138z.

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

Council of Science Editors:

Herrmann AT. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. [Thesis]. University of California – eScholarship, University of California; 2015. Available from: http://www.escholarship.org/uc/item/8fd8138z

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


Hong Kong University of Science and Technology

23. Au Yeung, Siu Fung. Synthesis and characterization of organo-borate solids.

Degree: 2011, Hong Kong University of Science and Technology

 Boric acid ‘flux’ synthesis was developed by our group and assisted the preparation of new borate materials solids. In this thesis apply the methodology to… (more)

Subjects/Keywords: Borates  – Synthesis ; Organic compounds  – Synthesis ; Salicylates

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Au Yeung, S. F. (2011). Synthesis and characterization of organo-borate solids. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7306 ; https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html

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):

Au Yeung, Siu Fung. “Synthesis and characterization of organo-borate solids.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed April 03, 2020. http://repository.ust.hk/ir/Record/1783.1-7306 ; https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Au Yeung, Siu Fung. “Synthesis and characterization of organo-borate solids.” 2011. Web. 03 Apr 2020.

Vancouver:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Apr 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-7306 ; https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html.

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

Council of Science Editors:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7306 ; https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html

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


University of Oxford

24. Bentley, Scott Alexander. Asymmetric conjugate addition reactions.

Degree: 2011, University of Oxford

 This thesis is concerned with the asymmetric conjugate addition reactions of a range of chiral nucloeophiles. Chapter 1 introduces the conjugate addition reaction as a… (more)

Subjects/Keywords: 547.2; Organic synthesis : Organic synthesis : asymmetric synthesis : organic chemistry : conjugate addition : chemical methodology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bentley, S. A. (2011). Asymmetric conjugate addition reactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560927

Chicago Manual of Style (16th Edition):

Bentley, Scott Alexander. “Asymmetric conjugate addition reactions.” 2011. Doctoral Dissertation, University of Oxford. Accessed April 03, 2020. http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560927.

MLA Handbook (7th Edition):

Bentley, Scott Alexander. “Asymmetric conjugate addition reactions.” 2011. Web. 03 Apr 2020.

Vancouver:

Bentley SA. Asymmetric conjugate addition reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Apr 03]. Available from: http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560927.

Council of Science Editors:

Bentley SA. Asymmetric conjugate addition reactions. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560927


Victoria University of Wellington

25. Asbury, Ashton Nikylla. Toward the Synthesis of Rimarikiamide A.

Degree: 2017, Victoria University of Wellington

 Rimarikiamide A is a linear diterpenoid marine natural product featuring an unusual taurine structural moiety. Rimarikiamide A was isolated from the sea sponge Latrunculia brevis… (more)

Subjects/Keywords: Synthesis; Organic; Rimarikiamide A

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Asbury, A. N. (2017). Toward the Synthesis of Rimarikiamide A. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/6443

Chicago Manual of Style (16th Edition):

Asbury, Ashton Nikylla. “Toward the Synthesis of Rimarikiamide A.” 2017. Masters Thesis, Victoria University of Wellington. Accessed April 03, 2020. http://hdl.handle.net/10063/6443.

MLA Handbook (7th Edition):

Asbury, Ashton Nikylla. “Toward the Synthesis of Rimarikiamide A.” 2017. Web. 03 Apr 2020.

Vancouver:

Asbury AN. Toward the Synthesis of Rimarikiamide A. [Internet] [Masters thesis]. Victoria University of Wellington; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10063/6443.

Council of Science Editors:

Asbury AN. Toward the Synthesis of Rimarikiamide A. [Masters Thesis]. Victoria University of Wellington; 2017. Available from: http://hdl.handle.net/10063/6443


University of Hawaii

26. Siṃha, Īśvara. Synthetic approaches toward napthazarin derivatives.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography: leaves [114]-116.

ix, 116 l illus., tables

The sea urchin pigments, spinochromes A, C, D, and E (I, II, III, and IV) are… (more)

Subjects/Keywords: Naphthazarin; Organic compounds  – Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Siṃha, I. (2009). Synthetic approaches toward napthazarin derivatives. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11394

Chicago Manual of Style (16th Edition):

Siṃha, Īśvara. “Synthetic approaches toward napthazarin derivatives.” 2009. Doctoral Dissertation, University of Hawaii. Accessed April 03, 2020. http://hdl.handle.net/10125/11394.

MLA Handbook (7th Edition):

Siṃha, Īśvara. “Synthetic approaches toward napthazarin derivatives.” 2009. Web. 03 Apr 2020.

Vancouver:

Siṃha I. Synthetic approaches toward napthazarin derivatives. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10125/11394.

Council of Science Editors:

Siṃha I. Synthetic approaches toward napthazarin derivatives. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11394


University of Hong Kong

27. 陳肇人; Chan, Diana. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.

Degree: PhD, 2016, University of Hong Kong

The first transannular (4+3) cycloadditions based on the activation of epoxy enolsilanes have been realized. Six macrocyclic epoxy ketones were converted to enolsilanes, then treated… (more)

Subjects/Keywords: Organic cyclic compounds - Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

陳肇人; Chan, D. (2016). Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238343

Chicago Manual of Style (16th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. http://hdl.handle.net/10722/238343.

MLA Handbook (7th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Web. 03 Apr 2020.

Vancouver:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10722/238343.

Council of Science Editors:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238343


University of Hong Kong

28. Guo, Jiawen. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.

Degree: M. Phil., 2013, University of Hong Kong

Recently, during the past10 years, with the intensified attention paid to the environment and industrial development, there has been growing interest in organocatalysis. One important… (more)

Subjects/Keywords: Chemistry, Organic; Catalysts - Synthesis; Catalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guo, J. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Masters Thesis). University of Hong Kong. Retrieved from Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023

Chicago Manual of Style (16th Edition):

Guo, Jiawen. “Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.” 2013. Masters Thesis, University of Hong Kong. Accessed April 03, 2020. Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023.

MLA Handbook (7th Edition):

Guo, Jiawen. “Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction.” 2013. Web. 03 Apr 2020.

Vancouver:

Guo J. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2020 Apr 03]. Available from: Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023.

Council of Science Editors:

Guo J. Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. [Masters Thesis]. University of Hong Kong; 2013. Available from: Guo, J. [郭嘉雯]. (2013). Chiral spirodiphosphine dioxides organocatalysis and hydrogen transfer reduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153730 ; http://dx.doi.org/10.5353/th_b5153730 ; http://hdl.handle.net/10722/196023

29. Katari, Naresh Kumar. Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis.

Degree: Chemistry, 2011, Jawaharlal Nehru Technological University

Investigation embodied in this thesis entitled “Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis” divided into four chapters, which are… (more)

Subjects/Keywords: Dithiocarbamates; Organic synthesis; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Katari, N. K. (2011). Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/3484

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):

Katari, Naresh Kumar. “Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis.” 2011. Thesis, Jawaharlal Nehru Technological University. Accessed April 03, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/3484.

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

MLA Handbook (7th Edition):

Katari, Naresh Kumar. “Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis.” 2011. Web. 03 Apr 2020.

Vancouver:

Katari NK. Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2011. [cited 2020 Apr 03]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3484.

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

Council of Science Editors:

Katari NK. Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis. [Thesis]. Jawaharlal Nehru Technological University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3484

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

30. Kumar, Vinoth V. Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -.

Degree: Chemistry, 2012, Acharya Nagarjuna University

None

Bibliography given

Advisors/Committee Members: Raghavan S.

Subjects/Keywords: Organic Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kumar, V. V. (2012). Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -. (Thesis). Acharya Nagarjuna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/48913

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):

Kumar, Vinoth V. “Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -.” 2012. Thesis, Acharya Nagarjuna University. Accessed April 03, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/48913.

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

MLA Handbook (7th Edition):

Kumar, Vinoth V. “Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -.” 2012. Web. 03 Apr 2020.

Vancouver:

Kumar VV. Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -. [Internet] [Thesis]. Acharya Nagarjuna University; 2012. [cited 2020 Apr 03]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/48913.

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

Council of Science Editors:

Kumar VV. Perparation and Utility of Chlorosulfides in Organic Synthesis Stereoselesctive Synthesis of the C1 C8 and C9 C19 Subunits of Pelourside A; -. [Thesis]. Acharya Nagarjuna University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/48913

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

[1] [2] [3] [4] [5] … [75]

.