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You searched for subject:(Organic synthesis). Showing records 1 – 30 of 2065 total matches.

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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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Aish GA. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2019 Apr 20]. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Gilmet J. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . [Internet] [Thesis]. Brock University; 2010. [cited 2019 Apr 20]. 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.

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


University of Colorado

4. 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

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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 http://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 20, 2019. http://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. 20 Apr 2019.

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 2019 Apr 20]. Available from: http://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: http://scholar.colorado.edu/chem_gradetds/191


Nelson Mandela Metropolitan University

5. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2013. [cited 2019 Apr 20]. 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


Rutgers University

6. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

7. 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 April 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

8. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Ebisu K. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2019 Apr 20]. 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

9. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

10. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


Georgia Tech

11. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

12. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Hale BJ. Influence of heterocycle substitution in π-functional materials for organic photovoltaics. [Internet] [Thesis]. Iowa State University; 2015. [cited 2019 Apr 20]. 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

13. 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.

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

14. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


Hong Kong University of Science and Technology

15. 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

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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 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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2019 Apr 20]. Available from: 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: 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 Hong Kong

16. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2019 Apr 20]. 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

17. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

18. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

19. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2019 Apr 20]. 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


University of Oxford

20. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Bentley SA. Asymmetric conjugate addition reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Apr 20]. 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

21. Trupina, Snjezana. Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases.

Degree: Chemistry and Biology, 2010, Linköping UniversityLinköping University

  Abnormal aggregation of misfolded proteins is related to numerous neurodegenerative diseases, which include Alzheimer’s, Parkinson’s disease and prion diseases. Luminescent conjugated probes (LCPs) have… (more)

Subjects/Keywords: Organic synthesis; Organisk syntes

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APA (6th Edition):

Trupina, S. (2010). Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases. (Thesis). Linköping UniversityLinköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989

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):

Trupina, Snjezana. “Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases.” 2010. Thesis, Linköping UniversityLinköping University. Accessed April 20, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989.

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

MLA Handbook (7th Edition):

Trupina, Snjezana. “Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases.” 2010. Web. 20 Apr 2019.

Vancouver:

Trupina S. Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases. [Internet] [Thesis]. Linköping UniversityLinköping University; 2010. [cited 2019 Apr 20]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989.

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

Council of Science Editors:

Trupina S. Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases. [Thesis]. Linköping UniversityLinköping University; 2010. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989

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


Victoria University of Wellington

22. 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

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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 20, 2019. http://hdl.handle.net/10063/6443.

MLA Handbook (7th Edition):

Asbury, Ashton Nikylla. “Toward the Synthesis of Rimarikiamide A.” 2017. Web. 20 Apr 2019.

Vancouver:

Asbury AN. Toward the Synthesis of Rimarikiamide A. [Internet] [Masters thesis]. Victoria University of Wellington; 2017. [cited 2019 Apr 20]. 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

23. 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

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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 20, 2019. 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. 20 Apr 2019.

Vancouver:

Katari NK. Studies directed towards the synthesis of dithiocarbamates and its application in organic synthesis. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2011. [cited 2019 Apr 20]. 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

24. 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

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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 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


University of KwaZulu-Natal

25. Naicker, Tricia. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .

Degree: Chemistry, 2008, University of KwaZulu-Natal

 There is enormous interest in the design and development of efficient chiral ligands for asymmetric catalysis, as a result, this field has become one of… (more)

Subjects/Keywords: Organic compounds – Synthesis.; Catalysis.; Chemistry.

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APA (6th Edition):

Naicker, T. (2008). Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/427

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):

Naicker, Tricia. “Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .” 2008. Thesis, University of KwaZulu-Natal. Accessed April 20, 2019. http://hdl.handle.net/10413/427.

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

MLA Handbook (7th Edition):

Naicker, Tricia. “Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .” 2008. Web. 20 Apr 2019.

Vancouver:

Naicker T. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . [Internet] [Thesis]. University of KwaZulu-Natal; 2008. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/10413/427.

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

Council of Science Editors:

Naicker T. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . [Thesis]. University of KwaZulu-Natal; 2008. Available from: http://hdl.handle.net/10413/427

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


Mahatma Gandhi University

26. Joshy, C L. Activation of carboxyl groups in organic synthesis.

Degree: 2010, Mahatma Gandhi University

 Activation of different carboxylic acids and amino acids using some selected heterocyclic compounds which contain light sensitive chromophore were investigated under different conditions with a… (more)

Subjects/Keywords: organic synthesis; Carboxyl groups

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

APA (6th Edition):

Joshy, C. L. (2010). Activation of carboxyl groups in organic synthesis. (Thesis). Mahatma Gandhi University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/241

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):

Joshy, C L. “Activation of carboxyl groups in organic synthesis.” 2010. Thesis, Mahatma Gandhi University. Accessed April 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/241.

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

MLA Handbook (7th Edition):

Joshy, C L. “Activation of carboxyl groups in organic synthesis.” 2010. Web. 20 Apr 2019.

Vancouver:

Joshy CL. Activation of carboxyl groups in organic synthesis. [Internet] [Thesis]. Mahatma Gandhi University; 2010. [cited 2019 Apr 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/241.

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

Council of Science Editors:

Joshy CL. Activation of carboxyl groups in organic synthesis. [Thesis]. Mahatma Gandhi University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/241

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


University of Guelph

27. Haner, Jamie. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions .

Degree: 2011, University of Guelph

 This thesis describes investigations on the topic of the versatile organic scaffold, 7-oxabenzonorbornadiene. The synthesis of 2-alkyl substituted furans via iron-catalyzed coupling of Grignard reagents… (more)

Subjects/Keywords: Oxabenzonorbornadiene; Cycloaddition; Organic Chemistry; Synthesis

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

APA (6th Edition):

Haner, J. (2011). Synthesis of Substituted Oxabenzonorbornadienes and their Reactions . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958

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):

Haner, Jamie. “Synthesis of Substituted Oxabenzonorbornadienes and their Reactions .” 2011. Thesis, University of Guelph. Accessed April 20, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958.

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

MLA Handbook (7th Edition):

Haner, Jamie. “Synthesis of Substituted Oxabenzonorbornadienes and their Reactions .” 2011. Web. 20 Apr 2019.

Vancouver:

Haner J. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions . [Internet] [Thesis]. University of Guelph; 2011. [cited 2019 Apr 20]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958.

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

Council of Science Editors:

Haner J. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions . [Thesis]. University of Guelph; 2011. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958

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


University of Western Australia

28. Nielsen, Linda Birgitta. Synthesis of some naturally occurring quinones.

Degree: PhD, 2008, University of Western Australia

Naturally occurring quinones have attracted considerable interest due to their widespread occurrence, structural diversity and often potent biological activities. The research outlined in this thesis… (more)

Subjects/Keywords: Organic synthesis; Quinones; Natural products

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APA (6th Edition):

Nielsen, L. B. (2008). Synthesis of some naturally occurring quinones. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=6076&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Nielsen, Linda Birgitta. “Synthesis of some naturally occurring quinones.” 2008. Doctoral Dissertation, University of Western Australia. Accessed April 20, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=6076&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Nielsen, Linda Birgitta. “Synthesis of some naturally occurring quinones.” 2008. Web. 20 Apr 2019.

Vancouver:

Nielsen LB. Synthesis of some naturally occurring quinones. [Internet] [Doctoral dissertation]. University of Western Australia; 2008. [cited 2019 Apr 20]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=6076&local_base=GEN01-INS01.

Council of Science Editors:

Nielsen LB. Synthesis of some naturally occurring quinones. [Doctoral Dissertation]. University of Western Australia; 2008. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=6076&local_base=GEN01-INS01


Nelson Mandela Metropolitan University

29. Pohl, Pieter Lourens. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.

Degree: Faculty of Science, 2015, Nelson Mandela Metropolitan University

 In this study, we investigated the potential of a novel chiral host compound (+)-(2R,3R)-1,1,4,4-tetraphenylbutane-1,2,3,4-tetraol (TETROL) and its derivatives for use in racemate resolution using host-guest… (more)

Subjects/Keywords: Chemistry, Organic; Chirality; Asymmetric synthesis

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APA (6th Edition):

Pohl, P. L. (2015). Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/2879

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):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Thesis, Nelson Mandela Metropolitan University. Accessed April 20, 2019. http://hdl.handle.net/10948/2879.

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

MLA Handbook (7th Edition):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Web. 20 Apr 2019.

Vancouver:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2015. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/10948/2879.

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

Council of Science Editors:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Thesis]. Nelson Mandela Metropolitan University; 2015. Available from: http://hdl.handle.net/10948/2879

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


Victoria University of Wellington

30. Hewitt, Russell James. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.

Degree: 2010, Victoria University of Wellington

 Cyclopropanes and carbohydrates are materials of great interest to chemists. Ring opening reactions of cyclopropanated carbohydrates have excellent potential for synthesis, due to the many… (more)

Subjects/Keywords: Organic compounds; Synthesis; Carbohydrates; Cyclopropane

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

APA (6th Edition):

Hewitt, R. J. (2010). Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1249

Chicago Manual of Style (16th Edition):

Hewitt, Russell James. “Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.” 2010. Doctoral Dissertation, Victoria University of Wellington. Accessed April 20, 2019. http://hdl.handle.net/10063/1249.

MLA Handbook (7th Edition):

Hewitt, Russell James. “Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.” 2010. Web. 20 Apr 2019.

Vancouver:

Hewitt RJ. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2010. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/10063/1249.

Council of Science Editors:

Hewitt RJ. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. [Doctoral Dissertation]. Victoria University of Wellington; 2010. Available from: http://hdl.handle.net/10063/1249

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