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You searched for subject:(Problems of organic synthesis). Showing records 1 – 30 of 282525 total matches.

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National University of Ireland – Galway

1. Mc Cleary, Nadine. Design, synthesis and catalytic activity of novel oxazoline based ligands .

Degree: 2015, National University of Ireland – Galway

 This thesis can be viewed as two separate studies. Firstly, the design, synthesis and catalytic activity of novel 2-pyridyl mono(oxazoline). A family of mono(oxazoline) ligands… (more)

Subjects/Keywords: Asymmetric catalysis; Organic synthesis; School of Chemistry

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APA (6th Edition):

Mc Cleary, N. (2015). Design, synthesis and catalytic activity of novel oxazoline based ligands . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5210

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):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands .” 2015. Thesis, National University of Ireland – Galway. Accessed October 29, 2020. http://hdl.handle.net/10379/5210.

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

MLA Handbook (7th Edition):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands .” 2015. Web. 29 Oct 2020.

Vancouver:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands . [Internet] [Thesis]. National University of Ireland – Galway; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10379/5210.

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

Council of Science Editors:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands . [Thesis]. National University of Ireland – Galway; 2015. Available from: http://hdl.handle.net/10379/5210

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


Dalhousie University

2. 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 October 29, 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. 29 Oct 2020.

Vancouver:

Aish GA. The Synthesis and Enzymatic Evaluation of Biologically Relevant Sugar 1-Phosphonates. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2020 Oct 29]. 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


National University of Ireland – Galway

3. Farrell, Mark. The anomerisation of glycosidic linkages .

Degree: 2014, National University of Ireland – Galway

 This thesis deals with the anomerisation of glycosidic linkages using TiCl4 and SnCl4. Methods involving the Lewis acid induced anomerisations of glycosides have been published… (more)

Subjects/Keywords: Carbohydrate; Synthesis; Organic chemistry; Department of Chemistry; School of Natural Sciences

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APA (6th Edition):

Farrell, M. (2014). The anomerisation of glycosidic linkages . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/4641

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):

Farrell, Mark. “The anomerisation of glycosidic linkages .” 2014. Thesis, National University of Ireland – Galway. Accessed October 29, 2020. http://hdl.handle.net/10379/4641.

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

MLA Handbook (7th Edition):

Farrell, Mark. “The anomerisation of glycosidic linkages .” 2014. Web. 29 Oct 2020.

Vancouver:

Farrell M. The anomerisation of glycosidic linkages . [Internet] [Thesis]. National University of Ireland – Galway; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10379/4641.

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

Council of Science Editors:

Farrell M. The anomerisation of glycosidic linkages . [Thesis]. National University of Ireland – Galway; 2014. Available from: http://hdl.handle.net/10379/4641

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


Brock University

4. 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 October 29, 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. 29 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 29]. 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

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

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Mahanjana, Lungelwa. “Reactions towards the synthesis of the uncommon P57 cymarose moiety.” 2013. Thesis, Nelson Mandela Metropolitan University. Accessed October 29, 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. 29 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 29]. 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

6. 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 October 29, 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. 29 Oct 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 Oct 29]. 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

7. 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 29, 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. 29 Oct 2020.

Vancouver:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Oct 29]. 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

8. 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 29, 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. 29 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 29]. 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


Miami University

9. Kumi, Godwin K. Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds.

Degree: MS, Chemistry, 2004, Miami University

 (S)-Minquartynoic acid, (S)-18-Hydroxyminquartynoic acid, and (E)-15,16-Dihydromin-quartynoic acid are polyacetylenic natural products. In recent in vitro tests, all three polyacetylenes show potent cytotoxicity, against 10 different… (more)

Subjects/Keywords: Chemistry, Organic; Synthesis of polyacetylenes

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APA (6th Edition):

Kumi, G. K. (2004). Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds. (Masters Thesis). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1091738753

Chicago Manual of Style (16th Edition):

Kumi, Godwin K. “Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds.” 2004. Masters Thesis, Miami University. Accessed October 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=miami1091738753.

MLA Handbook (7th Edition):

Kumi, Godwin K. “Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds.” 2004. Web. 29 Oct 2020.

Vancouver:

Kumi GK. Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds. [Internet] [Masters thesis]. Miami University; 2004. [cited 2020 Oct 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1091738753.

Council of Science Editors:

Kumi GK. Total Syntheses of (-)-18-Hydroxyminquartynoic Acid, (S)-E-15,16-Dihydrominquartynoic Acid, and Analogs of Minquartynoic Acid, and Antibacterial Properties of Some Selected Polyacetylenic Compounds. [Masters Thesis]. Miami University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1091738753


Dalhousie University

10. 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 October 29, 2020. http://hdl.handle.net/10222/37454.

MLA Handbook (7th Edition):

Moulins, Jonathan. “Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes.” 2013. Web. 29 Oct 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 Oct 29]. Available from: http://hdl.handle.net/10222/37454.

Council of Science Editors:

Moulins J. Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/37454


University of Manitoba

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

Degree: Chemistry, 2017, University of Manitoba

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

Subjects/Keywords: Chemistry; Organic Synthesis

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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 October 29, 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. 29 Oct 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 Oct 29]. Available from: http://hdl.handle.net/1993/32766.

Council of Science Editors:

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


Boston University

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

Degree: PhD, Chemistry, 2019, Boston University

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

Subjects/Keywords: Chemistry; Organic synthesis

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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 October 29, 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. 29 Oct 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 Oct 29]. 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


University of Wisconsin – Milwaukee

13. Uddin, Md Nazim. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.

Degree: PhD, Chemistry, 2015, University of Wisconsin – Milwaukee

  The development of efficient catalytic enantioselective synthesis of all carbon quaternary centers is a significant challenge in chemical synthesis due to the difficulties of… (more)

Subjects/Keywords: Asymmetric Allylic Alkylation; Asymmetric Synthesis; Organometallic Chemistry; Phase Transfer Catalysis; Synthesis of Chiral Tryptophans and Total Synthesis of Tryprostatin; Synthesis of Quaternary Stereocenter; Chemistry; Organic Chemistry

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APA (6th Edition):

Uddin, M. N. (2015). I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/931

Chicago Manual of Style (16th Edition):

Uddin, Md Nazim. “I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.” 2015. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed October 29, 2020. https://dc.uwm.edu/etd/931.

MLA Handbook (7th Edition):

Uddin, Md Nazim. “I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.” 2015. Web. 29 Oct 2020.

Vancouver:

Uddin MN. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2015. [cited 2020 Oct 29]. Available from: https://dc.uwm.edu/etd/931.

Council of Science Editors:

Uddin MN. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2015. Available from: https://dc.uwm.edu/etd/931


Victoria University of Wellington

14. Khan, Ashna Ashneen. Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid.

Degree: 2008, Victoria University of Wellington

 Daphnioldhanin A 1.6 is a recent alkaloid obtained from Daphyniphyllum plants. The core structure as shown consists of a 5,5,7 tricyclic ring system, which is… (more)

Subjects/Keywords: Alkaloid synthesis; Synthesis of natural products; Organic compounds; Organic chemical synthesis

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APA (6th Edition):

Khan, A. A. (2008). Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/818

Chicago Manual of Style (16th Edition):

Khan, Ashna Ashneen. “Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid.” 2008. Masters Thesis, Victoria University of Wellington. Accessed October 29, 2020. http://hdl.handle.net/10063/818.

MLA Handbook (7th Edition):

Khan, Ashna Ashneen. “Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid.” 2008. Web. 29 Oct 2020.

Vancouver:

Khan AA. Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid. [Internet] [Masters thesis]. Victoria University of Wellington; 2008. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10063/818.

Council of Science Editors:

Khan AA. Cascade Approaches Towards the Synthesis of Daphnioldhanin A Alkaloid. [Masters Thesis]. Victoria University of Wellington; 2008. Available from: http://hdl.handle.net/10063/818

15. Αγγελόπουλος, Βασίλειος. Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους.

Degree: 2011, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

 According to studies, the Johnstone-EI-Banna problem solving theory seems to exist, however it has low power. The main cause is the difficulty to define the… (more)

Subjects/Keywords: Επίπεδα νοητικής ανάπτυξης κατά Piaget; Χωρητικότητα μνήμης εργασίας; Βαθμός εξάρτησης από το πεδίο; Ιεραρχική προσέγγιση διδασκαλίας; Περιγραφική χημεία; Επεξηγήσεις; Μοντέλο Jonston – El Banna; Προβλήματα οργανικής σύνθεσης; Levels of cognitive development in Piaget; Working Memory Capacity; Dependence from the field; Hierarchical approach teaching; Descriptive chemistry; Explanation; Model Jonston – El Banna; Problems of organic synthesis

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APA (6th Edition):

Αγγελόπουλος, . . (2011). Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/26974

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):

Αγγελόπουλος, Βασίλειος. “Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους.” 2011. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed October 29, 2020. http://hdl.handle.net/10442/hedi/26974.

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

MLA Handbook (7th Edition):

Αγγελόπουλος, Βασίλειος. “Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους.” 2011. Web. 29 Oct 2020.

Vancouver:

Αγγελόπουλος . Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2011. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10442/hedi/26974.

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

Council of Science Editors:

Αγγελόπουλος . Μελέτη της περιγραφικής χημείας και των προβλημάτων οργανικής σύνθεσης σε σχέση με τρεις ψυχομετρικές παραμέτρους. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2011. Available from: http://hdl.handle.net/10442/hedi/26974

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


University of Saskatchewan

16. Diddi, Naveen 1981-. THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS.

Degree: 2019, University of Saskatchewan

 Dolabriferol C is a member of a small family of marine natural products known as non-contiguous polypropionates that are esters of a polypropionate carboxylic acid… (more)

Subjects/Keywords: Total Synthesis; One-pot Stereoselective Aldol Reactions; Polypropionates; Enantioselective Synthesis of Dolabriferol C; Meso Bisenolates; Meso 1,5-Diketones; Enantioselective Desymmetrization; Kinetic Resolution; Enantiotopic Group Selectivity; Asymmetric Synthesis; Organic Synthesis.

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APA (6th Edition):

Diddi, N. 1. (2019). THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12151

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):

Diddi, Naveen 1981-. “THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS.” 2019. Thesis, University of Saskatchewan. Accessed October 29, 2020. http://hdl.handle.net/10388/12151.

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

MLA Handbook (7th Edition):

Diddi, Naveen 1981-. “THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS.” 2019. Web. 29 Oct 2020.

Vancouver:

Diddi N1. THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10388/12151.

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

Council of Science Editors:

Diddi N1. THE TOTAL SYNTHESIS OF DOLABRIFEROL C VIA ONE-POT ENANTIOSELECTIVE BISALDOL REACTIONS. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12151

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


Georgia Tech

17. 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 29, 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. 29 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 29]. 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

18. 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 October 29, 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. 29 Oct 2020.

Vancouver:

Hale BJ. Influence of heterocycle substitution in π-functional materials for organic photovoltaics. [Internet] [Thesis]. Iowa State University; 2015. [cited 2020 Oct 29]. 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


RMIT University

19. Rao, V. Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones.

Degree: 2017, RMIT University

 Electrophilic cyclization in recent years has grown exponentially and has become the most sought-after method for the synthesis of heterocyclic molecules. The attention to electrophilic… (more)

Subjects/Keywords: Fields of Research; Iodine; Electrophilic cyclization; iodocyclization; organic synthesis; furan; iodine monochloride; iodoketones; haloketones

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APA (6th Edition):

Rao, V. (2017). Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:162275

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):

Rao, V. “Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones.” 2017. Thesis, RMIT University. Accessed October 29, 2020. http://researchbank.rmit.edu.au/view/rmit:162275.

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

MLA Handbook (7th Edition):

Rao, V. “Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones.” 2017. Web. 29 Oct 2020.

Vancouver:

Rao V. Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones. [Internet] [Thesis]. RMIT University; 2017. [cited 2020 Oct 29]. Available from: http://researchbank.rmit.edu.au/view/rmit:162275.

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

Council of Science Editors:

Rao V. Exploring aminoalkynols for the synthesis of iodo-dihydrofuran heterocycles by electrophilic cyclization and exploiting its unusual reactivity for the synthesis of α-iodoketones. [Thesis]. RMIT University; 2017. Available from: http://researchbank.rmit.edu.au/view/rmit:162275

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


University of Delaware

20. Reid, William Blackburn. Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters.

Degree: PhD, University of Delaware, Department of Chemistry and Biochemistry, 2018, University of Delaware

 Unsaturated heteroatomic compounds are an important class of molecules in many disciplines of chemistry. In particular, organosilanes and boronic esters serve as valued reagents and… (more)

Subjects/Keywords: Pure sciences; Heck reactions; Synthesis of complicated organic materials; Unsaturated heteroatomic compounds

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APA (6th Edition):

Reid, W. B. (2018). Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23801

Chicago Manual of Style (16th Edition):

Reid, William Blackburn. “Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters.” 2018. Doctoral Dissertation, University of Delaware. Accessed October 29, 2020. http://udspace.udel.edu/handle/19716/23801.

MLA Handbook (7th Edition):

Reid, William Blackburn. “Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters.” 2018. Web. 29 Oct 2020.

Vancouver:

Reid WB. Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters. [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2020 Oct 29]. Available from: http://udspace.udel.edu/handle/19716/23801.

Council of Science Editors:

Reid WB. Recent advances in heteroatomic-Heck reactions towards the synthesis of unsaturated silanes and boronic esters. [Doctoral Dissertation]. University of Delaware; 2018. Available from: http://udspace.udel.edu/handle/19716/23801


University of Adelaide

21. Zhang, Xiaozhou. Peptidomimetic protease inhibitors: activity and mechanism of inhibition.

Degree: 2015, University of Adelaide

 The study of protein mechanism and function is central to the development of biosensing tools and therapeutics for the treatment of diseases. This thesis describes… (more)

Subjects/Keywords: organic synthesis; protease inhibitors; mechanism of inhibition; peptidomimetics; photochromism; Research by Publication

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APA (6th Edition):

Zhang, X. (2015). Peptidomimetic protease inhibitors: activity and mechanism of inhibition. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/111994

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):

Zhang, Xiaozhou. “Peptidomimetic protease inhibitors: activity and mechanism of inhibition.” 2015. Thesis, University of Adelaide. Accessed October 29, 2020. http://hdl.handle.net/2440/111994.

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

MLA Handbook (7th Edition):

Zhang, Xiaozhou. “Peptidomimetic protease inhibitors: activity and mechanism of inhibition.” 2015. Web. 29 Oct 2020.

Vancouver:

Zhang X. Peptidomimetic protease inhibitors: activity and mechanism of inhibition. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2440/111994.

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

Council of Science Editors:

Zhang X. Peptidomimetic protease inhibitors: activity and mechanism of inhibition. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/111994

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


Florida International University

22. yasmeen, Samina. Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide.

Degree: MS, Chemistry, 2016, Florida International University

  Fulgides and fulgimides comprise one class of thermally irreversible photochromic organic compounds. Light dependent isomerization, has made these organic molecules promising materials for several… (more)

Subjects/Keywords: Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide; Organic Chemistry

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APA (6th Edition):

yasmeen, S. (2016). Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/2725 ; 10.25148/etd.FIDC001260 ; FIDC001260

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):

yasmeen, Samina. “Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide.” 2016. Thesis, Florida International University. Accessed October 29, 2020. https://digitalcommons.fiu.edu/etd/2725 ; 10.25148/etd.FIDC001260 ; FIDC001260.

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

MLA Handbook (7th Edition):

yasmeen, Samina. “Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide.” 2016. Web. 29 Oct 2020.

Vancouver:

yasmeen S. Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide. [Internet] [Thesis]. Florida International University; 2016. [cited 2020 Oct 29]. Available from: https://digitalcommons.fiu.edu/etd/2725 ; 10.25148/etd.FIDC001260 ; FIDC001260.

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

Council of Science Editors:

yasmeen S. Synthesis and Characterization of a Hydrolytically Stable Photochromic Copolymer Containing an N-alkylindolylfulgimide. [Thesis]. Florida International University; 2016. Available from: https://digitalcommons.fiu.edu/etd/2725 ; 10.25148/etd.FIDC001260 ; FIDC001260

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


Florida Atlantic University

23. Li, Songye. Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents.

Degree: PhD, 2011, Florida Atlantic University

Summary: We report here the development of very efficient aryl- and quinolinyl- sulfonate based leaving groups, termed Nucleophile Assisting Leaving Groups (NALGs), which substantially accelerate… (more)

Subjects/Keywords: Chemical kinetics; Chemical reaction, Condition and laws of; Organic compounds – Synthesis; Organotransition metal compounds; Intermediates (Chemistry); Organic reaction mechanisms

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APA (6th Edition):

Li, S. (2011). Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents. (Doctoral Dissertation). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3183130

Chicago Manual of Style (16th Edition):

Li, Songye. “Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents.” 2011. Doctoral Dissertation, Florida Atlantic University. Accessed October 29, 2020. http://purl.flvc.org/FAU/3183130.

MLA Handbook (7th Edition):

Li, Songye. “Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents.” 2011. Web. 29 Oct 2020.

Vancouver:

Li S. Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents. [Internet] [Doctoral dissertation]. Florida Atlantic University; 2011. [cited 2020 Oct 29]. Available from: http://purl.flvc.org/FAU/3183130.

Council of Science Editors:

Li S. Development and applications of nucleophile assisting leaving groups (NALGs) with Titanium (IV) and Grignard reagents. [Doctoral Dissertation]. Florida Atlantic University; 2011. Available from: http://purl.flvc.org/FAU/3183130


University of Adelaide

24. 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 October 29, 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. 29 Oct 2020.

Vancouver:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2020 Oct 29]. 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

25. 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 October 29, 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. 29 Oct 2020.

Vancouver:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Internet] [Thesis]. University of California – eScholarship, University of California; 2017. [cited 2020 Oct 29]. 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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Herrmann, Aaron Thomas. “Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.” 2015. Thesis, University of California – eScholarship, University of California. Accessed October 29, 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. 29 Oct 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 Oct 29]. 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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Au Yeung, Siu Fung. “Synthesis and characterization of organo-borate solids.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed October 29, 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. 29 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 29]. 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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Bentley, Scott Alexander. “Asymmetric conjugate addition reactions.” 2011. Doctoral Dissertation, University of Oxford. Accessed October 29, 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. 29 Oct 2020.

Vancouver:

Bentley SA. Asymmetric conjugate addition reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Oct 29]. 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


Nelson Mandela Metropolitan University

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

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Thesis, Nelson Mandela Metropolitan University. Accessed October 29, 2020. http://hdl.handle.net/10948/2879.

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

MLA Handbook (7th Edition):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Web. 29 Oct 2020.

Vancouver:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10948/2879.

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

Council of Science Editors:

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

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


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

30. 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 October 29, 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. 29 Oct 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 Oct 29]. 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

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