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You searched for subject:(Organic compounds Synthesis ). Showing records 1 – 30 of 36242 total matches.

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Brock University

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Metcalf, Thomas A. “Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .” 2011. Thesis, Brock University. Accessed October 25, 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. 25 Oct 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 Oct 25]. 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

2. 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 October 25, 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. 25 Oct 2020.

Vancouver:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2013. [cited 2020 Oct 25]. 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 Oxford

3. 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 October 25, 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. 25 Oct 2020.

Vancouver:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Oct 25]. 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

4. 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 October 25, 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. 25 Oct 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 Oct 25]. 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


University of Johannesburg

5. Crous, Renier. Approaches to the synthesis of selected nitrogenous heterocycles.

Degree: PhD, 2012, University of Johannesburg

 The first part of the research described in this thesis involves the development of a new methodology for the synthesis of N-hydroxy pyrrolidines, starting from… (more)

Subjects/Keywords: Organic compounds - Synthesis.; Nitrogen compounds.; Heterocyclic compounds.

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APA (6th Edition):

Crous, R. (2012). Approaches to the synthesis of selected nitrogenous heterocycles. (Doctoral Dissertation). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/6287

Chicago Manual of Style (16th Edition):

Crous, Renier. “Approaches to the synthesis of selected nitrogenous heterocycles.” 2012. Doctoral Dissertation, University of Johannesburg. Accessed October 25, 2020. http://hdl.handle.net/10210/6287.

MLA Handbook (7th Edition):

Crous, Renier. “Approaches to the synthesis of selected nitrogenous heterocycles.” 2012. Web. 25 Oct 2020.

Vancouver:

Crous R. Approaches to the synthesis of selected nitrogenous heterocycles. [Internet] [Doctoral dissertation]. University of Johannesburg; 2012. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10210/6287.

Council of Science Editors:

Crous R. Approaches to the synthesis of selected nitrogenous heterocycles. [Doctoral Dissertation]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/6287


Drexel University

6. 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 October 25, 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. 25 Oct 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 Oct 25]. 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


University of Johannesburg

7. 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 (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 October 25, 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. 25 Oct 2020.

Vancouver:

Braithwaite DH. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Oct 25]. 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

8. 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 (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 October 25, 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. 25 Oct 2020.

Vancouver:

Williams DBG. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Oct 25]. 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

9. 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 (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 October 25, 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. 25 Oct 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 Oct 25]. 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

10. 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 (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 October 25, 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. 25 Oct 2020.

Vancouver:

Sagandira CR. Exploring acyl azides chemistry in continuous flow systems. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2017. [cited 2020 Oct 25]. 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


Victoria University of Wellington

11. 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 (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 October 25, 2020. 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. 25 Oct 2020.

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 2020 Oct 25]. 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


Hong Kong University of Science and Technology

12. Zhou, Jiangbin. Synthesis of the C8-C12 fragment of amphidinolactone B.

Degree: 2015, Hong Kong University of Science and Technology

 In connection with the total synthesis of a marine macrolide, amphidinolactone B, this thesis deals with the synthesis of the C8–C12 fragment of this molecule.… (more)

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

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APA (6th Edition):

Zhou, J. (2015). Synthesis of the C8-C12 fragment of amphidinolactone B. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-80263 ; https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/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):

Zhou, Jiangbin. “Synthesis of the C8-C12 fragment of amphidinolactone B.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-80263 ; https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/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):

Zhou, Jiangbin. “Synthesis of the C8-C12 fragment of amphidinolactone B.” 2015. Web. 25 Oct 2020.

Vancouver:

Zhou J. Synthesis of the C8-C12 fragment of amphidinolactone B. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-80263 ; https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/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:

Zhou J. Synthesis of the C8-C12 fragment of amphidinolactone B. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-80263 ; https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/th_redirect.html

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

13. Li, Zhilong. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.

Degree: 2017, Hong Kong University of Science and Technology

 This thesis consists of four chapters, describing the development of new synthetic methodology and total syntheses of natural products: chapter one is focused on the… (more)

Subjects/Keywords: Natural products ; Synthesis ; Organic compounds

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APA (6th Edition):

Li, Z. (2017). Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-88075 ; https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/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):

Li, Zhilong. “Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-88075 ; https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/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):

Li, Zhilong. “Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.” 2017. Web. 25 Oct 2020.

Vancouver:

Li Z. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-88075 ; https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/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:

Li Z. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: http://repository.ust.hk/ir/Record/1783.1-88075 ; https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/th_redirect.html

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

14. Wu, Yandong. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.

Degree: 2014, Hong Kong University of Science and Technology

 Marine microorganisms are widely viewed as an emerging source of novel natural products. A variety of butenolides [or furan-2(5H)-ones], featured with an α,β-unsaturated lactone core,… (more)

Subjects/Keywords: Organic compounds ; Synthesis ; Lactones ; Stereochemistry

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APA (6th Edition):

Wu, Y. (2014). Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/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):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/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):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Web. 25 Oct 2020.

Vancouver:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/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:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html

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. Ye, Ning. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.

Degree: 2014, Hong Kong University of Science and Technology

 Total synthesis of natural products is the Holy Grail of chemical science. Not only does it serve for structural elucidation, but also as an enabling… (more)

Subjects/Keywords: Organic compounds ; Synthesis ; Stereoisomers ; Lactones

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APA (6th Edition):

Ye, N. (2014). Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/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):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/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):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Web. 25 Oct 2020.

Vancouver:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/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:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html

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

16. Wang, Yong CHEM. Regio- and stereoselective functionalization of thioalkynes and ynamides.

Degree: 2017, Hong Kong University of Science and Technology

 Functionalization of alkynes is a very important field in organic chemistry, because it provides straightforward synthesis of multi-substituted alkenes, which are widely present in biological… (more)

Subjects/Keywords: Alkynes ; Catalysts ; Organic compounds ; Synthesis

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APA (6th Edition):

Wang, Y. C. (2017). Regio- and stereoselective functionalization of thioalkynes and ynamides. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-97159 ; https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/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):

Wang, Yong CHEM. “Regio- and stereoselective functionalization of thioalkynes and ynamides.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-97159 ; https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/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):

Wang, Yong CHEM. “Regio- and stereoselective functionalization of thioalkynes and ynamides.” 2017. Web. 25 Oct 2020.

Vancouver:

Wang YC. Regio- and stereoselective functionalization of thioalkynes and ynamides. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-97159 ; https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/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:

Wang YC. Regio- and stereoselective functionalization of thioalkynes and ynamides. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: http://repository.ust.hk/ir/Record/1783.1-97159 ; https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/th_redirect.html

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

17. Bendel, Lars Erik CHEM. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.

Degree: 2018, Hong Kong University of Science and Technology

 The SmI2-mediated reductive coupling reaction between non-conjugated aldehydes and two 2-(dialkylamido)aryl 2,3-disubstituted α,β-unsaturated esters has been investigated. In contrast to the corresponding 2- or 3-monosubstituted… (more)

Subjects/Keywords: Organic compounds ; Synthesis ; Inorganic compounds ; Aldehydes ; Samarium

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APA (6th Edition):

Bendel, L. E. C. (2018). Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-97892 ; https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/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):

Bendel, Lars Erik CHEM. “Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.” 2018. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-97892 ; https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/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):

Bendel, Lars Erik CHEM. “Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.” 2018. Web. 25 Oct 2020.

Vancouver:

Bendel LEC. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2018. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-97892 ; https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/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:

Bendel LEC. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. [Thesis]. Hong Kong University of Science and Technology; 2018. Available from: http://repository.ust.hk/ir/Record/1783.1-97892 ; https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/th_redirect.html

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

18. 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 October 25, 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. 25 Oct 2020.

Vancouver:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Oct 25]. 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


Durban University of Technology

19. Makhanya, Talent Raymond. Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides.

Degree: 2019, Durban University of Technology

Submitted in fulfillment of the requirements for the award of the degree of Doctor in Philosophy in Chemistry, Durban University of Technology, Durban, South Africa,… (more)

Subjects/Keywords: Pyrazoles – Synthesis; Naphthyridines – Synthesis; Heterocyclic compounds – Synthesis; Organic compounds

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APA (6th Edition):

Makhanya, T. R. (2019). Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides. (Thesis). Durban University of Technology. Retrieved from http://hdl.handle.net/10321/3211

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):

Makhanya, Talent Raymond. “Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides.” 2019. Thesis, Durban University of Technology. Accessed October 25, 2020. http://hdl.handle.net/10321/3211.

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

MLA Handbook (7th Edition):

Makhanya, Talent Raymond. “Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides.” 2019. Web. 25 Oct 2020.

Vancouver:

Makhanya TR. Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides. [Internet] [Thesis]. Durban University of Technology; 2019. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10321/3211.

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

Council of Science Editors:

Makhanya TR. Synthesis, characterisation and biological activity of selected pyrazoles and naphthyrides. [Thesis]. Durban University of Technology; 2019. Available from: http://hdl.handle.net/10321/3211

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


Georgia Tech

20. 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 October 25, 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. 25 Oct 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 Oct 25]. 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


Nelson Mandela Metropolitan University

21. Kleyi, Phumelele Eldridge. Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I).

Degree: MSc, Faculty of Science, 2009, Nelson Mandela Metropolitan University

 Solvent-free reactions possess advantages compared to the solvent route, such as shorter reaction times, less use of energy, better yields, etc. Herein, the synthesis and… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Organic solvents; Solution (Chemistry); Chemistry, Organic; Coordination compounds

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APA (6th Edition):

Kleyi, P. E. (2009). Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I). (Masters Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/1053

Chicago Manual of Style (16th Edition):

Kleyi, Phumelele Eldridge. “Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I).” 2009. Masters Thesis, Nelson Mandela Metropolitan University. Accessed October 25, 2020. http://hdl.handle.net/10948/1053.

MLA Handbook (7th Edition):

Kleyi, Phumelele Eldridge. “Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I).” 2009. Web. 25 Oct 2020.

Vancouver:

Kleyi PE. Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I). [Internet] [Masters thesis]. Nelson Mandela Metropolitan University; 2009. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10948/1053.

Council of Science Editors:

Kleyi PE. Solvent-free synthesis of bisferrocenylimines and their coordination to rhodium (I). [Masters Thesis]. Nelson Mandela Metropolitan University; 2009. Available from: http://hdl.handle.net/10948/1053


Ryerson University

22. Wright, Nande Abena. Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling.

Degree: 2016, Ryerson University

 The various strategies and reaction conditions towards the synthesis of benzene-, naphthalene-, and phenanthrene-based dicyclohexylbiaryl phosphanes are presented. A chiral third generation Buchwald-type precatalyst has… (more)

Subjects/Keywords: Bioactive compounds  – Synthesis; Organic compounds  – Synthesis; Palladium catalysts

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APA (6th Edition):

Wright, N. A. (2016). Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A5728

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):

Wright, Nande Abena. “Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling.” 2016. Thesis, Ryerson University. Accessed October 25, 2020. https://digital.library.ryerson.ca/islandora/object/RULA%3A5728.

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

MLA Handbook (7th Edition):

Wright, Nande Abena. “Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling.” 2016. Web. 25 Oct 2020.

Vancouver:

Wright NA. Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling. [Internet] [Thesis]. Ryerson University; 2016. [cited 2020 Oct 25]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A5728.

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

Council of Science Editors:

Wright NA. Synthesis and Application of Chiral Palladium-Phosphane Precatalyst in Enantioselective C-N Cross-Coupling. [Thesis]. Ryerson University; 2016. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A5728

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


Stellenbosch University

23. Kleinhans, Dewald Johannes. Studies in the synthesis of benzoxazole compounds.

Degree: PhD, Chemistry and Polymer Science, 2015, Stellenbosch University

ENGLISH ABSTRACT: Benzoxazoles are an important class of π-electron-excessive, benzene-fused heterocyclic compounds found in natural products and display a wide range of pharmacological applications. It… (more)

Subjects/Keywords: Benzoxazole  – Synthesis; Coordination compounds; Chiral ligands; Organic synthesis; Heterocyclic compounds; UCTD

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APA (6th Edition):

Kleinhans, D. J. (2015). Studies in the synthesis of benzoxazole compounds. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/97900

Chicago Manual of Style (16th Edition):

Kleinhans, Dewald Johannes. “Studies in the synthesis of benzoxazole compounds.” 2015. Doctoral Dissertation, Stellenbosch University. Accessed October 25, 2020. http://hdl.handle.net/10019.1/97900.

MLA Handbook (7th Edition):

Kleinhans, Dewald Johannes. “Studies in the synthesis of benzoxazole compounds.” 2015. Web. 25 Oct 2020.

Vancouver:

Kleinhans DJ. Studies in the synthesis of benzoxazole compounds. [Internet] [Doctoral dissertation]. Stellenbosch University; 2015. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10019.1/97900.

Council of Science Editors:

Kleinhans DJ. Studies in the synthesis of benzoxazole compounds. [Doctoral Dissertation]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/97900


Hong Kong University of Science and Technology

24. Ren, Jingyun CHEM. Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework.

Degree: 2015, Hong Kong University of Science and Technology

 Total syntheses of natural products is one of the most important subjects for chemical science. It is very useful for structural elucidation. Moreover, it could… (more)

Subjects/Keywords: Natural products ; Synthesis ; Organic compounds ; Organochlorine compounds ; Stereochemistry ; Asymmetric synthesis

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APA (6th Edition):

Ren, J. C. (2015). Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-94654 ; https://doi.org/10.14711/thesis-b1514906 ; http://repository.ust.hk/ir/bitstream/1783.1-94654/1/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):

Ren, Jingyun CHEM. “Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed October 25, 2020. http://repository.ust.hk/ir/Record/1783.1-94654 ; https://doi.org/10.14711/thesis-b1514906 ; http://repository.ust.hk/ir/bitstream/1783.1-94654/1/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):

Ren, Jingyun CHEM. “Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework.” 2015. Web. 25 Oct 2020.

Vancouver:

Ren JC. Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Oct 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-94654 ; https://doi.org/10.14711/thesis-b1514906 ; http://repository.ust.hk/ir/bitstream/1783.1-94654/1/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:

Ren JC. Studies on diastereoselective dichlorination and total syntheses of natural products with 6,8-dioxabicyclo[3.2.1]octane framework. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-94654 ; https://doi.org/10.14711/thesis-b1514906 ; http://repository.ust.hk/ir/bitstream/1783.1-94654/1/th_redirect.html

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


Florida Atlantic University

25. Maity, Pradip. Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C.

Degree: PhD, 2011, Florida Atlantic University

Summary: We report here the development of new and more general synthetic pathways for the preparation of allenyl and alkynyl carbonyls. These highly dense functionalized… (more)

Subjects/Keywords: Organic compounds – Synthesis; Carbonyl compounds – Synthesis; Cardiovascular system – Diseases – Treatment

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APA (6th Edition):

Maity, P. (2011). Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C. (Doctoral Dissertation). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3332717

Chicago Manual of Style (16th Edition):

Maity, Pradip. “Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C.” 2011. Doctoral Dissertation, Florida Atlantic University. Accessed October 25, 2020. http://purl.flvc.org/FAU/3332717.

MLA Handbook (7th Edition):

Maity, Pradip. “Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C.” 2011. Web. 25 Oct 2020.

Vancouver:

Maity P. Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C. [Internet] [Doctoral dissertation]. Florida Atlantic University; 2011. [cited 2020 Oct 25]. Available from: http://purl.flvc.org/FAU/3332717.

Council of Science Editors:

Maity P. Synthesis and new reactions of allenyl carbonyls: studies towards the total synthesis of anti-thrombotic natural products Vitisinol D and C. [Doctoral Dissertation]. Florida Atlantic University; 2011. Available from: http://purl.flvc.org/FAU/3332717


Columbia University

26. Radtke, Mark Alexander. Synthesis and Reactivity of Highly Stabilized Cyclopentadienes.

Degree: 2018, Columbia University

 This dissertation focuses on the development of cyclopentadienes as an emerging class of compounds for use in catalysis. Previous work in the Lambert group had… (more)

Subjects/Keywords: Cyclopentadiene; Chemistry; Organic compounds – Synthesis; Organic compounds – Reactivity

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APA (6th Edition):

Radtke, M. A. (2018). Synthesis and Reactivity of Highly Stabilized Cyclopentadienes. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8JT179K

Chicago Manual of Style (16th Edition):

Radtke, Mark Alexander. “Synthesis and Reactivity of Highly Stabilized Cyclopentadienes.” 2018. Doctoral Dissertation, Columbia University. Accessed October 25, 2020. https://doi.org/10.7916/D8JT179K.

MLA Handbook (7th Edition):

Radtke, Mark Alexander. “Synthesis and Reactivity of Highly Stabilized Cyclopentadienes.” 2018. Web. 25 Oct 2020.

Vancouver:

Radtke MA. Synthesis and Reactivity of Highly Stabilized Cyclopentadienes. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2020 Oct 25]. Available from: https://doi.org/10.7916/D8JT179K.

Council of Science Editors:

Radtke MA. Synthesis and Reactivity of Highly Stabilized Cyclopentadienes. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8JT179K


Columbia University

27. Thomas, Stephen Basil. Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes.

Degree: 2015, Columbia University

 PART I Controllable Synthesis of Complex Members of the Resveratrol Oligomer Family Chapter 1. Synthesis and Biological Evaluation of Resveratrol Family Oligomeric Natural Products This… (more)

Subjects/Keywords: Natural products – Synthesis; Biochemistry; Chemistry, Organic; Organic compounds – Synthesis; Chemistry

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APA (6th Edition):

Thomas, S. B. (2015). Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8JW8D2V

Chicago Manual of Style (16th Edition):

Thomas, Stephen Basil. “Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes.” 2015. Doctoral Dissertation, Columbia University. Accessed October 25, 2020. https://doi.org/10.7916/D8JW8D2V.

MLA Handbook (7th Edition):

Thomas, Stephen Basil. “Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes.” 2015. Web. 25 Oct 2020.

Vancouver:

Thomas SB. Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2020 Oct 25]. Available from: https://doi.org/10.7916/D8JW8D2V.

Council of Science Editors:

Thomas SB. Exploring an Interface Between Synthetic Chemistry and Chemical Biology: The Synthesis of Complex Natural Products and Novel Chemical Probes. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8JW8D2V


Ryerson University

28. Kanellis, Vassilios. Toward the Synthesis of Novel Benzisoselenazolones.

Degree: 2016, Ryerson University

 Ebselen is a synthetic selenium-containing organic compound that has been studied as a potential treatment for a number of conditions. Ebselen is an antioxidant, capable… (more)

Subjects/Keywords: Bioactive compounds  – Biotechnology; Selenium compounds; Organic compounds  – Synthesis

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APA (6th Edition):

Kanellis, V. (2016). Toward the Synthesis of Novel Benzisoselenazolones. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A5729

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):

Kanellis, Vassilios. “Toward the Synthesis of Novel Benzisoselenazolones.” 2016. Thesis, Ryerson University. Accessed October 25, 2020. https://digital.library.ryerson.ca/islandora/object/RULA%3A5729.

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

MLA Handbook (7th Edition):

Kanellis, Vassilios. “Toward the Synthesis of Novel Benzisoselenazolones.” 2016. Web. 25 Oct 2020.

Vancouver:

Kanellis V. Toward the Synthesis of Novel Benzisoselenazolones. [Internet] [Thesis]. Ryerson University; 2016. [cited 2020 Oct 25]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A5729.

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

Council of Science Editors:

Kanellis V. Toward the Synthesis of Novel Benzisoselenazolones. [Thesis]. Ryerson University; 2016. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A5729

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

29. Sar, Anobick. Generation of Diverse Molecular Complexity from Simple Hydrocarbons.

Degree: 2011, Marquette University

 In an effort to make diverse molecular complexity from simple hydrocarbons, tricarbonyl(cyclohexadienyl)iron(+1) cation was prepared in two steps from 1, 3-cycloxehadiene. Reactivity of the symmetric… (more)

Subjects/Keywords: Molecular structure; Hydrocarbons; Chemistry; Organic; Organic compounds  – Synthesis; Chemistry  – Dissertations organic chemistry; organic synthesis; Chemistry

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

APA (6th Edition):

Sar, A. (2011). Generation of Diverse Molecular Complexity from Simple Hydrocarbons. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/140

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):

Sar, Anobick. “Generation of Diverse Molecular Complexity from Simple Hydrocarbons.” 2011. Thesis, Marquette University. Accessed October 25, 2020. https://epublications.marquette.edu/dissertations_mu/140.

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

MLA Handbook (7th Edition):

Sar, Anobick. “Generation of Diverse Molecular Complexity from Simple Hydrocarbons.” 2011. Web. 25 Oct 2020.

Vancouver:

Sar A. Generation of Diverse Molecular Complexity from Simple Hydrocarbons. [Internet] [Thesis]. Marquette University; 2011. [cited 2020 Oct 25]. Available from: https://epublications.marquette.edu/dissertations_mu/140.

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

Council of Science Editors:

Sar A. Generation of Diverse Molecular Complexity from Simple Hydrocarbons. [Thesis]. Marquette University; 2011. Available from: https://epublications.marquette.edu/dissertations_mu/140

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


UCLA

30. Roberts, Courtney Arielle. Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.

Degree: Chemistry, 2016, UCLA

 In Chapter 1, rearrangements of 4-substituted bicyclo[2.2.2]oct-2-enyl-5-selenophenyl esters are explored. Reduction of the esters under radical-generating conditions initially generates a bicyclo[2.2.2]oct-5-en-2-yl radical which can rearrange… (more)

Subjects/Keywords: Organic chemistry; Bicyclic compounds; Rearrangements; Total synthesis

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APA (6th Edition):

Roberts, C. A. (2016). Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/5wb2n0rd

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):

Roberts, Courtney Arielle. “Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.” 2016. Thesis, UCLA. Accessed October 25, 2020. http://www.escholarship.org/uc/item/5wb2n0rd.

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

MLA Handbook (7th Edition):

Roberts, Courtney Arielle. “Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide.” 2016. Web. 25 Oct 2020.

Vancouver:

Roberts CA. Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide. [Internet] [Thesis]. UCLA; 2016. [cited 2020 Oct 25]. Available from: http://www.escholarship.org/uc/item/5wb2n0rd.

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

Council of Science Editors:

Roberts CA. Methodologies of Bicyclo[2.2.2]octane Compounds and Progress Toward the Total Synthesis of Parthenolide. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/5wb2n0rd

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

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