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You searched for subject:(Organic Synthesis). Showing records 1 – 30 of 2303 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 September 20, 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. 20 Sep 2020.

Vancouver:

Aish GA. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2020 Sep 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. 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 September 20, 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. 20 Sep 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 Sep 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


Nelson Mandela Metropolitan University

3. 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 September 20, 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. 20 Sep 2020.

Vancouver:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2013. [cited 2020 Sep 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


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 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 September 20, 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. 20 Sep 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 Sep 20]. 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

5. 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

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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 September 20, 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. 20 Sep 2020.

Vancouver:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Sep 20]. 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

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 September 20, 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. 20 Sep 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 Sep 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 September 20, 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. 20 Sep 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 Sep 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 Manitoba

8. 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 September 20, 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. 20 Sep 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 Sep 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


Boston University

9. 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

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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 September 20, 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. 20 Sep 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 Sep 20]. 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

10. 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 September 20, 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. 20 Sep 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 Sep 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

11. 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 September 20, 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. 20 Sep 2020.

Vancouver:

Hale BJ. Influence of heterocycle substitution in π-functional materials for organic photovoltaics. [Internet] [Thesis]. Iowa State University; 2015. [cited 2020 Sep 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 Adelaide

12. 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 September 20, 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. 20 Sep 2020.

Vancouver:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2020 Sep 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

13. 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

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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 September 20, 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. 20 Sep 2020.

Vancouver:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Internet] [Thesis]. University of California – eScholarship, University of California; 2017. [cited 2020 Sep 20]. 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

14. 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

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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 September 20, 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. 20 Sep 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 Sep 20]. 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

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 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 September 20, 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. 20 Sep 2020.

Vancouver:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Sep 20]. 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

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

Degree: PhD, 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 September 20, 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. 20 Sep 2020.

Vancouver:

Bentley SA. Asymmetric conjugate addition reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Sep 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


University of Toledo Health Science Campus

17. Farrell, Robert Liam. Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor.

Degree: MSP, Medicinal Chemistry, 2015, University of Toledo Health Science Campus

 Cancer is a general term used to describe a group of over 100 different diseases all of which have a similar characteristic about them; the… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Largazole, Synthesis

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APA (6th Edition):

Farrell, R. L. (2015). Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1440071080

Chicago Manual of Style (16th Edition):

Farrell, Robert Liam. “Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor.” 2015. Masters Thesis, University of Toledo Health Science Campus. Accessed September 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1440071080.

MLA Handbook (7th Edition):

Farrell, Robert Liam. “Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor.” 2015. Web. 20 Sep 2020.

Vancouver:

Farrell RL. Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2015. [cited 2020 Sep 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1440071080.

Council of Science Editors:

Farrell RL. Studies on the Total Synthesis of a New Largazole Analogue as a Potential Histone Deacetylase Inhibitor. [Masters Thesis]. University of Toledo Health Science Campus; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1440071080


University of Sydney

18. Norcott, Philip Laurence. On-Water Domino Reactions as Strategies for Total Synthesis .

Degree: 2015, University of Sydney

 On the instigation of Dr C. S. P. McErlean I have investigated the use of ‘in-water/on-water’ domino reactions in natural product total synthesis. Though inherently… (more)

Subjects/Keywords: synthesis; organic; catalysis; water; domino

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APA (6th Edition):

Norcott, P. L. (2015). On-Water Domino Reactions as Strategies for Total Synthesis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/14202

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):

Norcott, Philip Laurence. “On-Water Domino Reactions as Strategies for Total Synthesis .” 2015. Thesis, University of Sydney. Accessed September 20, 2020. http://hdl.handle.net/2123/14202.

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

MLA Handbook (7th Edition):

Norcott, Philip Laurence. “On-Water Domino Reactions as Strategies for Total Synthesis .” 2015. Web. 20 Sep 2020.

Vancouver:

Norcott PL. On-Water Domino Reactions as Strategies for Total Synthesis . [Internet] [Thesis]. University of Sydney; 2015. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2123/14202.

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

Council of Science Editors:

Norcott PL. On-Water Domino Reactions as Strategies for Total Synthesis . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/14202

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


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

19. Tsovaltzi, Erifili. Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων.

Degree: 2019, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

In the present study, pyrano-1,2- and pyrano-1,4-naphthoquinone derivatives, analogs of α- and β-lapachone, were synthesized. These compounds were prepared through domino Knoevenagel/hetero-Diels-Alder reactions catalyzed by… (more)

Subjects/Keywords: Οργανική σύνθεση; Organic synthesis

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APA (6th Edition):

Tsovaltzi, E. (2019). Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/46109

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):

Tsovaltzi, Erifili. “Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων.” 2019. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed September 20, 2020. http://hdl.handle.net/10442/hedi/46109.

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

MLA Handbook (7th Edition):

Tsovaltzi, Erifili. “Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων.” 2019. Web. 20 Sep 2020.

Vancouver:

Tsovaltzi E. Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2019. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10442/hedi/46109.

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

Council of Science Editors:

Tsovaltzi E. Εφαρμογές της χημείας της 2-υδροξυ-1, 4-ναφθοκινόνης και του φαινυλοϊωδωνιο-υλιδίου της στη σύνθεση νέων οργανικών ενώσεων. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2019. Available from: http://hdl.handle.net/10442/hedi/46109

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


Vanderbilt University

20. Benoy, Jennifer Rae. TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES.

Degree: PhD, Chemistry, 2019, Vanderbilt University

 I. Prostaglandin E2 (PGE2) is a cyclic, oxygenated metabolite of arachidonic acid that has been shown to play a role in the pathophysiology of many… (more)

Subjects/Keywords: arachidonic acid; organic synthesis

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APA (6th Edition):

Benoy, J. R. (2019). TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12544

Chicago Manual of Style (16th Edition):

Benoy, Jennifer Rae. “TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/12544.

MLA Handbook (7th Edition):

Benoy, Jennifer Rae. “TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES.” 2019. Web. 20 Sep 2020.

Vancouver:

Benoy JR. TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/12544.

Council of Science Editors:

Benoy JR. TOTAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE OF PROSTAGLANDIN D2 AND E2 METABOLITES. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/12544


Drexel University

21. Tsetsakos, Panagiota. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.

Degree: 2014, Drexel University

Previously, ethyl 1-nitro-1,2,3,5,6,7,8,8a-octahydro-1- naphthalenecarboxylate was synthesized via tandem Mitsunobu cyclization - [3,3]-sigmatropic rearrangement of ethyl 5-(cyclohex-1-en-1-yl)-5-hydroxy-2- nitropentenoate. It was obtained in 48% yield as a… (more)

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

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APA (6th Edition):

Tsetsakos, P. (2014). Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/4501

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):

Tsetsakos, Panagiota. “Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.” 2014. Thesis, Drexel University. Accessed September 20, 2020. http://hdl.handle.net/1860/4501.

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

MLA Handbook (7th Edition):

Tsetsakos, Panagiota. “Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.” 2014. Web. 20 Sep 2020.

Vancouver:

Tsetsakos P. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. [Internet] [Thesis]. Drexel University; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1860/4501.

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

Council of Science Editors:

Tsetsakos P. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. [Thesis]. Drexel University; 2014. Available from: http://hdl.handle.net/1860/4501

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

22. 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 September 20, 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. 20 Sep 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 Sep 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

23. 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 September 20, 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. 20 Sep 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 Sep 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


Mahatma Gandhi University

24. 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 (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 September 20, 2020. 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 Sep 2020.

Vancouver:

Joshy CL. Activation of carboxyl groups in organic synthesis. [Internet] [Thesis]. Mahatma Gandhi University; 2010. [cited 2020 Sep 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


Penn State University

25. Mason, Jeremy David. Total Synthesis of (±)-Alstoscholarisines A-E.

Degree: 2018, Penn State University

 Total syntheses of the biologically active monoterpenoid indole alkaloids (±)-alstoscholarisines A-E (1-5) have been completed in twelve to fourteen steps. The approach commenced with a… (more)

Subjects/Keywords: Indole Alkaloids; Organic Synthesis

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APA (6th Edition):

Mason, J. D. (2018). Total Synthesis of (±)-Alstoscholarisines A-E. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15645jdm505

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):

Mason, Jeremy David. “Total Synthesis of (±)-Alstoscholarisines A-E.” 2018. Thesis, Penn State University. Accessed September 20, 2020. https://submit-etda.libraries.psu.edu/catalog/15645jdm505.

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

MLA Handbook (7th Edition):

Mason, Jeremy David. “Total Synthesis of (±)-Alstoscholarisines A-E.” 2018. Web. 20 Sep 2020.

Vancouver:

Mason JD. Total Synthesis of (±)-Alstoscholarisines A-E. [Internet] [Thesis]. Penn State University; 2018. [cited 2020 Sep 20]. Available from: https://submit-etda.libraries.psu.edu/catalog/15645jdm505.

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

Council of Science Editors:

Mason JD. Total Synthesis of (±)-Alstoscholarisines A-E. [Thesis]. Penn State University; 2018. Available from: https://submit-etda.libraries.psu.edu/catalog/15645jdm505

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


McMaster University

26. Johnson, Emma. SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS.

Degree: MSc, 2019, McMaster University

Abstract The current rise in antibiotic resistance and lack of discovery of new antibiotics in recent years has caused an antibiotic crisis. A strategy for… (more)

Subjects/Keywords: edeine; organic chemistry; synthesis; antibiotic

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

APA (6th Edition):

Johnson, E. (2019). SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/25080

Chicago Manual of Style (16th Edition):

Johnson, Emma. “SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS.” 2019. Masters Thesis, McMaster University. Accessed September 20, 2020. http://hdl.handle.net/11375/25080.

MLA Handbook (7th Edition):

Johnson, Emma. “SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS.” 2019. Web. 20 Sep 2020.

Vancouver:

Johnson E. SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS. [Internet] [Masters thesis]. McMaster University; 2019. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/11375/25080.

Council of Science Editors:

Johnson E. SYNTHESIS OF EDEINE DERIVATIVES AS AN APPROACH TO TACKLE THE ANTIBIOTIC CRISIS. [Masters Thesis]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/25080


University of Johannesburg

27. Braithwaite, Dana Helen. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

The aim of this study waa to develop new methodology for the synthesis of chiral pyrrolidine derivatives Crom monosaccharides. An overview of the… (more)

Subjects/Keywords: Monosaccharides; Organic compounds - Synthesis

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

APA (6th Edition):

Braithwaite, D. H. (2014). New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10144

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):

Braithwaite, Dana Helen. “New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.” 2014. Thesis, University of Johannesburg. Accessed September 20, 2020. http://hdl.handle.net/10210/10144.

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

MLA Handbook (7th Edition):

Braithwaite, Dana Helen. “New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.” 2014. Web. 20 Sep 2020.

Vancouver:

Braithwaite DH. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10210/10144.

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

Council of Science Editors:

Braithwaite DH. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10144

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


University of Johannesburg

28. Williams, Dennis Bradley Glen. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

Palladium-mediated carbon-earbon (and carbon-heteroatom) bond formation! is to an increasing extent playing a vital role in synthetic organic chemistry. The chemistry is usually… (more)

Subjects/Keywords: Palladium; Organic compounds - Synthesis

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

APA (6th Edition):

Williams, D. B. G. (2014). Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/9145

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):

Williams, Dennis Bradley Glen. “Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.” 2014. Thesis, University of Johannesburg. Accessed September 20, 2020. http://hdl.handle.net/10210/9145.

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

MLA Handbook (7th Edition):

Williams, Dennis Bradley Glen. “Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.” 2014. Web. 20 Sep 2020.

Vancouver:

Williams DBG. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10210/9145.

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

Council of Science Editors:

Williams DBG. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/9145

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


University of Johannesburg

29. Thompson, Catherine. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

Barium titanate (BaTi03) is an important material in the electronics industry as a result of its excellent dielectric properties. It has been the… (more)

Subjects/Keywords: Barium metatitanate; Organic compounds - Synthesis

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

APA (6th Edition):

Thompson, C. (2014). Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10857

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):

Thompson, Catherine. “Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.” 2014. Thesis, University of Johannesburg. Accessed September 20, 2020. http://hdl.handle.net/10210/10857.

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

MLA Handbook (7th Edition):

Thompson, Catherine. “Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.” 2014. Web. 20 Sep 2020.

Vancouver:

Thompson C. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10210/10857.

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

Council of Science Editors:

Thompson C. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10857

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


Nelson Mandela Metropolitan University

30. Sagandira, Cloudius Ray. Exploring acyl azides chemistry in continuous flow systems.

Degree: Faculty of Science, 2017, Nelson Mandela Metropolitan University

Organic azides are important in the synthesis of many target molecules of great use in fine chemical and pharmaceutical production. The use of this class… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Flow chemistry

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

APA (6th Edition):

Sagandira, C. R. (2017). Exploring acyl azides chemistry in continuous flow systems. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/12065

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):

Sagandira, Cloudius Ray. “Exploring acyl azides chemistry in continuous flow systems.” 2017. Thesis, Nelson Mandela Metropolitan University. Accessed September 20, 2020. http://hdl.handle.net/10948/12065.

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

MLA Handbook (7th Edition):

Sagandira, Cloudius Ray. “Exploring acyl azides chemistry in continuous flow systems.” 2017. Web. 20 Sep 2020.

Vancouver:

Sagandira CR. Exploring acyl azides chemistry in continuous flow systems. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2017. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10948/12065.

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

Council of Science Editors:

Sagandira CR. Exploring acyl azides chemistry in continuous flow systems. [Thesis]. Nelson Mandela Metropolitan University; 2017. Available from: http://hdl.handle.net/10948/12065

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

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